https://www.bosterbio.com/products/primary-antibodies/anti-blvrb-picoband-trade-antibody-a08072-2-boster.html2026-03-17T05:14:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08072-2-blvrb-primary-antibodies-wb-testing-1.jpgAnti-BLVRB Antibody Picoband® Western blot analysis of BLVRB using anti-BLVRB antibody (A08072-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BLVRB antigen affinity purified polyclonal antibody (Catalog # A08072-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BLVRB at approximately 22 kDa. The expected band size for BLVRB is at 22-27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08072-2-blvrb-primary-antibodies-if-testing-2.jpgAnti-BLVRB Antibody Picoband® IF analysis of BLVRB using anti-BLVRB antibody (A08072-2). BLVRB was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BLVRB Antibody (A08072-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08072-2-blvrb-primary-antibodies-fcm-testing-3.pngAnti-BLVRB Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-BLVRB antibody (A08072-2). Overlay histogram showing MCF-7 cells stained with A08072-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BLVRB Antibody (A08072-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-cxcl1-picoband-trade-antibody-a00533-2-boster.html2026-03-17T05:14:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00533-2-cxcl1-primary-antibodies-ihc-testing-1.jpgAnti-CXCL1 Antibody IHC analysis of CXCL1 using anti-CXCL1 antibody (A00533-2). CXCL1 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CXCL1 Antibody (A00533-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-ccl7-picoband-trade-antibody-a02379-1-boster.html2026-03-17T05:14:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02379-1-ccl7-primary-antibodies-wb-testing-1.jpgAnti-Ccl7 Antibody Picoband® Western blot analysis of Ccl7 using anti-Ccl7 antibody (A02379-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. Lane 1: recombinant rat Ccl7 protein 10 ng, Lane 2: recombinant rat Ccl7 protein 5 ng. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ccl7 antigen affinity purified polyclonal antibody (Catalog # A02379-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Ccl7 at approximately 9 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-ccl23-picoband-trade-antibody-a05808-1-boster.html2026-03-17T05:14:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05808-1-ccl23-primary-antibodies-ihc-testing-1.jpgAnti-CCL23 Antibody IHC analysis of CCL23 using anti-CCL23 antibody (A05808-1). CCL23 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CCL23 Antibody (A05808-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05808-1-ccl23-primary-antibodies-ihc-testing-2.jpgAnti-CCL23 Antibody IHC analysis of CCL23 using anti-CCL23 antibody (A05808-1). CCL23 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CCL23 Antibody (A05808-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05808-1-ccl23-primary-antibodies-ihc-testing-3.jpgAnti-CCL23 Antibody IHC analysis of CCL23 using anti-CCL23 antibody (A05808-1). CCL23 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CCL23 Antibody (A05808-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-ccl15-picoband-trade-antibody-a05563-1-boster.html2026-03-17T05:14:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05563-1-ccl15-primary-antibodies-ihc-testing-1.jpgAnti-CCL15 Antibody IHC analysis of CCL15 using anti-CCL15 antibody (A05563-1). CCL15 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CCL15 Antibody (A05563-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05563-1-ccl15-primary-antibodies-ihc-testing-2.jpgAnti-CCL15 Antibody IHC analysis of CCL15 using anti-CCL15 antibody (A05563-1). CCL15 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CCL15 Antibody (A05563-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-tdp-43-tardbp-picoband-trade-antibody-a01001-3-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-wb-testing-1.jpgAnti-TDP-43/TARDBP Antibody Picoband® Western blot analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse pancrease lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TDP-43/TARDBP antigen affinity purified polyclonal antibody (Catalog # A01001-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TDP-43/TARDBP at approximately 43 kDa. The expected band size for TDP-43/TARDBP is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-ihc-testing-2.jpgAnti-TDP-43/TARDBP Antibody Picoband® IHC analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3). TDP-43/TARDBP was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDP-43/TARDBP Antibody (A01001-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-ihc-testing-3.jpgAnti-TDP-43/TARDBP Antibody Picoband® IHC analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3). TDP-43/TARDBP was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDP-43/TARDBP Antibody (A01001-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-ihc-testing-4.jpgAnti-TDP-43/TARDBP Antibody Picoband® IHC analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3). TDP-43/TARDBP was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDP-43/TARDBP Antibody (A01001-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-ihc-testing-5.jpgAnti-TDP-43/TARDBP Antibody Picoband® IHC analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3). TDP-43/TARDBP was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDP-43/TARDBP Antibody (A01001-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-ihc-testing-6.jpgAnti-TDP-43/TARDBP Antibody Picoband® IHC analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3). TDP-43/TARDBP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDP-43/TARDBP Antibody (A01001-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-ihc-testing-7.jpgAnti-TDP-43/TARDBP Antibody Picoband® IHC analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3). TDP-43/TARDBP was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDP-43/TARDBP Antibody (A01001-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-if-testing-8.jpgAnti-TDP-43/TARDBP Antibody Picoband® IF analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3) and anti-Beta Tubulin antibody (M01857-3). TDP-43/TARDBP was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TDP-43/TARDBP Antibody (A01001-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-ip-testing-1.jpgAnti-TDP-43/TARDBP Antibody Picoband®Immunoprecipitating (IP) TDP-43/TARDBP in HepG2 whole cell lysate. Western blot analysis of TDP-43/TARDBP using anti-TDP-43/TARDBP antibody (A01001-3); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-TDP-43/TARDBP antibody in HepG2 whole cell lysate; Lane 3: anti-TDP-43/TARDBP antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TDP-43/TARDBP antigen affinity purified polyclonal antibody (A01001-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for TDP-43/TARDBP at approximately 40 kDa. The expected band size for TDP-43/TARDBP is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01001-3-tardbp-primary-antibodies-fcm-testing-9.pngAnti-TDP-43/TARDBP Antibody Picoband® Flow Cytometry analysis of JK cells using anti-TDP-43/TARDBP antibody (A01001-3). Overlay histogram showing JK cells stained with A01001-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TDP-43/TARDBP Antibody (A01001-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1236372026-03-13T05:04:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02019-2-redd1-ddit4-primary-antibodies-wb-testing-1.jpgAnti-REDD1/DDIT4 specific Antibody Western blot analysis of REDD1/DDIT4 using anti-REDD1/DDIT4 antibody (A02019-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-REDD1/DDIT4 antigen affinity purified polyclonal antibody (A02019-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for REDD1/DDIT4 at approximately 35 kDa. The expected band size for REDD1/DDIT4 is at 25 kDa. https://www.bosterbio.com/catalog/product/view/id/1236382026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00016-5-p16ink4a-cdkn2a-primary-antibodies-wb-testing-1.jpgAnti-p16INK4a/CDKN2A Antibody Western blot analysis of p16INK4a/CDKN2A using anti-p16INK4a/CDKN2A antibody (A00016-5). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p16INK4a/CDKN2A antigen affinity purified polyclonal antibody (A00016-5) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for p16INK4a/CDKN2A at approximately 17 kDa. The expected band size for p16INK4a/CDKN2A is at 17 kDa. https://www.bosterbio.com/catalog/product/view/id/1236392026-03-13T05:04:58+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236402026-03-17T05:14:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01246-4-ocln-primary-antibodies-wb-testing-1.jpgAnti-Occludin/OCLN Antibody Picoband® Western blot analysis of Occludin/OCLN using anti-Occludin/OCLN antibody (A01246-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Occludin/OCLN antigen affinity purified polyclonal antibody (A01246-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Occludin/OCLN at approximately 59 kDa. The expected band size for Occludin/OCLN is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01246-4-ocln-primary-antibodies-ihc-testing-3_1.jpgAnti-Occludin/OCLN Antibody Picoband®IHC analysis of Occludin/OCLN using anti-Occludin/OCLN antibody (A01246-4). Occludin/OCLN was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Occludin/OCLN Antibody (A01246-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01246-4-ocln-primary-antibodies-ihc-testing-4.jpgAnti-Occludin/OCLN Antibody Picoband®IHC analysis of Occludin/OCLN using anti-Occludin/OCLN antibody (A01246-4). Occludin/OCLN was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Occludin/OCLN Antibody (A01246-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01246-4-13020_2025_1180_fig7_html.pngAnti-Occludin/OCLN Antibody Picoband®Effect of Huanglian-Jiedu decoction on intestinal barrier in APP/PS1 mice. A Representative image of HE staining in the mouse intestine, and representative images of immunohistochemistry of intestinal Occludin and ZO-1 (Scale bar = 50 μm). B Statistical analysis of the relative expression level of Occludin. C Statistical analysis of the relative expression level of ZO-1. D The expressions of ZO-1 and Occludin proteins in the intestine were detected by Western blotting. E Semi-quantitative analysis of the gray value of Occludin. F Semi-quantitative analysis of the gray value of ZO-1. Data are presented as mean ± SD (n = 3). ## P < 0.01 (vs control group), * P < 0.05 and ** P < 0.01 (vs model group) Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-025-01180-4'>40770806</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01246-4-fft270164-fig-0008-m.jpgAnti-Occludin/OCLN Antibody Picoband®Effects of MT water extract on regulating macrophage polarization, maintaining intestinal barrier integrity, and alleviating oxidative stress in the colons of DSS-induced UC mice. (A) IHC staining of iNOS, Arg1, occludin, and ZO-1 expressions in mouse colon tissues. Quantitative analysis of the integrated optical density (IOD) of (B) iNOS, (C) Arg1, (D) occludin, and (E) ZO-1 in each group. The levels of (F) IL-6, (G) IL-10, (H) MDA, and (I) GSH were measured and analyzed. Data were presented as means ± SD for three independent trials. One-way ANOVA followed by Tukey's multiple comparison test was performed to compare the differences between groups. *p < 0.05 versus control and #p < 0.05 versus DSS alone group. Arg1, arginase 1; DSS, dextran sulfate sodium; IL, interleukin; iNOS, inducible nitric oxide synthase; MDA, malondialdehyde; MT, Medulla Tetrapanacis. Index in Food Frontiers under a CC BY license. DOI: <a href='0'>10.1002/fft2.70164</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01246-4-ocln-primary-antibodies-testing-ip-2.jpgAnti-Occludin/OCLN Antibody Picoband® Immunoprecipitating Occludin/OCLN in HepG2 whole cell lysate. Western blot analysis of Occludin/OCLN using anti-Occludin/OCLN antibody (A01246-4). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-Occludin/OCLN antibody in HepG2 whole cell lysate, Lane 3: anti-Occludin/OCLN antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Occludin/OCLN antigen affinity purified polyclonal antibody (A01246-4) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Light Chain Specific). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for Occludin/OCLN at approximately 59 kDa. The expected band size for Occludin/OCLN is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01246-4-ocln-primary-antibodies-ihc-testing-3.jpgAnti-Occludin/OCLN Antibody Picoband® IHC analysis of Occludin/OCLN using anti-Occludin/OCLN antibody (A01246-4). Occludin/OCLN was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Occludin/OCLN Antibody (A01246-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1236412026-03-13T05:04:58+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236422026-03-17T05:14:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02558-1-sesn2-primary-antibodies-wb-testing-1.jpgAnti-Sestrin 2/SESN2 Antibody Picoband®Western blot analysis of SESN2 using anti-SESN2 antibody (A02558-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SESN2 antigen affinity purified polyclonal antibody (A02558-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SESN2 at approximately 60 kDa. The expected band size for SESN2 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02558-1-sesn2-primary-antibodies-ihc-testing-1.jpgAnti-Sestrin 2/SESN2 Antibody Picoband®IHC analysis of SESN2 using anti-SESN2 antibody (A02558-1). SESN2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SESN2 Antibody (A02558-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02558-1-sesn2-primary-antibodies-ihc-testing-2.jpgAnti-Sestrin 2/SESN2 Antibody Picoband®IHC analysis of SESN2 using anti-SESN2 antibody (A02558-1). SESN2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SESN2 Antibody (A02558-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02558-1-sesn2-primary-antibodies-ihc-testing-3.jpgAnti-Sestrin 2/SESN2 Antibody Picoband®IHC analysis of SESN2 using anti-SESN2 antibody (A02558-1). SESN2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SESN2 Antibody (A02558-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02558-1-sesn2-primary-antibodies-if-testing-1.jpgAnti-Sestrin 2/SESN2 Antibody Picoband®IF analysis of SESN2 using anti-SESN2 antibody (A02558-1). SESN2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SESN2 Antibody (A02558-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02558-1-sesn2-primary-antibodies-fcm-testing-1.jpgAnti-Sestrin 2/SESN2 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-SESN2 antibody (A02558-1). Overlay histogram showing Jurkat cells stained with A02558-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SESN2 Antibody (A02558-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236432026-03-17T05:14:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-wb-testing-1.jpgAnti-YTHDF1 Antibody Picoband® Western blot analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YTHDF1 antigen affinity purified polyclonal antibody (A09853-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for YTHDF1 at approximately 67 kDa. The expected band size for YTHDF1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-ihc-testing-2.jpgAnti-YTHDF1 Antibody Picoband® IHC analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-ihc-testing-3.jpgAnti-YTHDF1 Antibody Picoband® IHC analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in a paraffin-embedded section of mouse epididymis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-ihc-testing-4.jpgAnti-YTHDF1 Antibody Picoband® IHC analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-wb-testing-1_1.jpgAnti-YTHDF1 Antibody Picoband®Western blot analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YTHDF1 antigen affinity purified polyclonal antibody (A09853-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for YTHDF1 at approximately 65 kDa. The expected band size for YTHDF1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-ihc-testing-1.jpgAnti-YTHDF1 Antibody Picoband®IHC analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-ihc-testing-2_1.jpgAnti-YTHDF1 Antibody Picoband®IHC analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-ihc-testing-3_1.jpgAnti-YTHDF1 Antibody Picoband®IHC analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-ihc-testing-4_1.jpgAnti-YTHDF1 Antibody Picoband®IHC analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-if-testing-1.jpgAnti-YTHDF1 Antibody Picoband®IF analysis of YTHDF1 using anti-YTHDF1 antibody (A09853-2). YTHDF1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-YTHDF1 Antibody (A09853-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09853-2-ythdf1-primary-antibodies-fcm-testing-1.jpgAnti-YTHDF1 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-YTHDF1 antibody (A09853-2). Overlay histogram showing HepG2 cells stained with A09853-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-YTHDF1 Antibody (A09853-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236452026-03-16T05:08:10+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236472026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00282-2-srebf1-primary-antibodies-wb-testing-1.jpgAnti-SREBF1 Antibody Western blot analysis of SREBF1 using anti-SREBF1 antibody (A00282-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: rat RH-35 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SREBF1 antigen affinity purified polyclonal antibody (A00282-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SREBF1 at approximately 122 kDa. The expected band size for SREBF1 is at 122 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00282-2-srebf1-primary-antibodies-ihc-testing-2.jpgAnti-SREBF1 Antibody IHC analysis of SREBF1 using anti-SREBF1 antibody (A00282-2). SREBF1 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-SREBF1 Antibody (A00282-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00282-2-srebf1-primary-antibodies-if-testing-1.jpgAnti-SREBF1 AntibodyIF analysis of SREBF1 using anti-SREBF1 antibody (A00282-2). SREBF1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-SREBF1 Antibody (A00282-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1236482026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01173-2-pkm2-primary-antibodies-wb-testing-1.jpgAnti-PKM2/PKM specific AntibodyWestern blot analysis of PKM2 using anti-PKM2 antibody (A01173-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human GES-1 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PKM2 antigen affinity purified polyclonal antibody (A01173-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PKM2 at approximately 58 kDa. The expected band size for PKM2 is at 58 kDa. https://www.bosterbio.com/catalog/product/view/id/1236492026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01168-2-vdac1-2-primary-antibodies-wb-testing-1.jpgAnti-VDAC1/2 Antibody Western blot analysis of VDAC1/2 using anti-VDAC1/2 antibody (A01168-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VDAC1/2 antigen affinity purified polyclonal antibody (A01168-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VDAC1/2 at approximately 31 kDa. The expected band size for VDAC1/2 is at 31 kDa. https://www.bosterbio.com/catalog/product/view/id/1236502026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02265-2-ifitm3-primary-antibodies-wb-testing-1.jpgAnti-IFITM3 AntibodyWestern blot analysis of IFITM3 using anti-IFITM3 antibody (A02265-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human SIHA whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFITM3 antigen affinity purified polyclonal antibody (A02265-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IFITM3 at approximately 17 kDa. The expected band size for IFITM3 is at 15 kDa. https://www.bosterbio.com/catalog/product/view/id/1236512026-03-10T04:35:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00165-7-irf3-primary-antibodies-wb-testing-1.jpgAnti-IRF3 Antibody Picoband® Western blot analysis of IRF3 using anti-IRF3 antibody (A00165-7). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRF3 antigen affinity purified polyclonal antibody (A00165-7) at 0.5 μg/ml overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IRF3 at approximately 50-55 kDa. The expected band size for IRF3 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00165-7-irf3-primary-antibodies-ihc-testing-2.jpgAnti-IRF3 Antibody Picoband® IHC analysis of IRF3 using anti-IRF3 antibody (A00165-7). IRF3 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF3 Antibody (A00165-7) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00165-7-irf3-primary-antibodies-ihc-testing-3.jpgAnti-IRF3 Antibody Picoband® IHC analysis of IRF3 using anti-IRF3 antibody (A00165-7). IRF3 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF3 Antibody (A00165-7) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1236522026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00046-2-kras-primary-antibodies-wb-testing-1.jpgAnti-KRAS Antibody Western blot analysis of KRAS using anti-KRAS antibody (A00046-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human SW620 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRAS antigen affinity purified polyclonal antibody (A00046-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRAS at approximately 20 kDa. The expected band size for KRAS is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00046-2-kras-primary-antibodies-ihc-testing-2.jpgAnti-KRAS Antibody IHC analysis of KRAS using anti-KRAS antibody (A00046-2). KRAS was detected in a paraffin-embedded section of human cervica squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-KRAS Antibody (A00046-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00046-2-kras-primary-antibodies-ihc-testing-3.jpgAnti-KRAS Antibody IHC analysis of KRAS using anti-KRAS antibody (A00046-2). KRAS was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-KRAS Antibody (A00046-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00046-2-kras-primary-antibodies-ihc-testing-4.jpgAnti-KRAS Antibody IHC analysis of KRAS using anti-KRAS antibody (A00046-2). KRAS was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-KRAS Antibody (A00046-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1236532026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00207-3-rhoa-primary-antibodies-wb-testing-1.jpgAnti-RHOA AntibodyWestern blot analysis of RHOA using anti-RHOA antibody (A00207-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RHOA antigen affinity purified polyclonal antibody (A00207-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RHOA at approximately 22 kDa. The expected band size for RHOA is at 22 kDa. https://www.bosterbio.com/catalog/product/view/id/1236552026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02394-5-ppp1r15a-primary-antibodies-wb-testing-1.jpgAnti-GADD34/PPP1R15A AntibodyWestern blot analysis of GADD34/PPP1R15A using anti-GADD34/PPP1R15A antibody (A02394-5). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GADD34/PPP1R15A antigen affinity purified polyclonal antibody (A02394-5) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GADD34/PPP1R15A at approximately 100 kDa. The expected band size for GADD34/PPP1R15A is at 73 kDa. https://www.bosterbio.com/catalog/product/view/id/1236562026-03-17T05:14:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00849-3-mx1-primary-antibodies-wb-testing-1_1.jpgAnti-MX1 Antibody Picoband®Western blot analysis of MX1 using anti-MX1 antibody (A00849-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MX1 antigen affinity purified polyclonal antibody (A00849-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MX1 at approximately 76 kDa. The expected band size for MX1 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00849-3-mx1-primary-antibodies-if-testing-1.jpgAnti-MX1 Antibody Picoband®IF analysis of MX1 using anti-MX1 antibody (A00849-3) and anti-Tubulin Alpha antibody (M03989-3). MX1 was detected in immunocytochemical section of SiHa cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MX1 Antibody (A00849-3) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00849-3-mx1-primary-antibodies-fcm-testing-1.jpgAnti-MX1 Antibody Picoband®Flow Cytometry analysis of SiHa cells using anti-MX1 antibody (A00849-3). Overlay histogram showing SiHa cells stained with A00849-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MX1 Antibody (A00849-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236572026-04-02T05:00:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09218-1-timm23-primary-antibodies-wb-testing-1.jpgAnti-TIM23/TIMM23 Antibody Picoband® Western blot analysis of TIMM23 using anti-TIMM23 antibody (A09218-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIMM23 antigen affinity purified polyclonal antibody (A09218-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TIMM23 at approximately 22 kDa. The expected band size for TIMM23 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09218-1-timm23-primary-antibodies-ihc-testing-2.jpgAnti-TIM23/TIMM23 Antibody Picoband® IHC analysis of TIMM23 using anti-TIMM23 antibody (A09218-1). TIMM23 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TIMM23 Antibody (A09218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09218-1-timm23-primary-antibodies-wb-testing-1_1.jpgAnti-TIM23/TIMM23 Antibody Picoband®Western blot analysis of TIM23/TIMM23 using anti-TIM23/TIMM23 antibody (A09218-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIM23/TIMM23 antigen affinity purified polyclonal antibody (A09218-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TIM23/TIMM23 at approximately 20 kDa. The expected band size for TIM23/TIMM23 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09218-1-timm23-primary-antibodies-ihc-testing-1.jpgAnti-TIM23/TIMM23 Antibody Picoband®IHC analysis of TIM23/TIMM23 using anti-TIM23/TIMM23 antibody (A09218-1). TIM23/TIMM23 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TIM23/TIMM23 Antibody (A09218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09218-1-timm23-primary-antibodies-ihc-testing-2_1.jpgAnti-TIM23/TIMM23 Antibody Picoband®IHC analysis of TIM23/TIMM23 using anti-TIM23/TIMM23 antibody (A09218-1). TIM23/TIMM23 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TIM23/TIMM23 Antibody (A09218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1236582026-03-16T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06687-1-sharpin-primary-antibodies-wb-testing-1.jpgAnti-SHARPIN Antibody Western blot analysis of SHARPIN using anti-SHARPIN antibody (A06687-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human THP-1 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHARPIN antigen affinity purified polyclonal antibody (A06687-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SHARPIN at approximately 40 kDa. The expected band size for SHARPIN is at 40 kDa. https://www.bosterbio.com/catalog/product/view/id/1236592026-03-13T05:04:58+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236612026-03-13T05:04:58+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236622026-03-17T05:14:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-wb-testing-1.jpgAnti-RB1CC1 Antibody Picoband® Western blot analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human SW620 whole cell lysates, Lane 4: rat RH-35 whole cell lysates, Lane 5: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RB1CC1 antigen affinity purified polyclonal antibody (A02414-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RB1CC1 at approximately 230 kDa. The expected band size for RB1CC1 is at 183 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-wb-testing-1_1.jpgAnti-RB1CC1 Antibody Picoband®Western blot analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RB1CC1 antigen affinity purified polyclonal antibody (A02414-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RB1CC1 at approximately 230 kDa. The expected band size for RB1CC1 is at 183 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-ihc-testing-1.jpgAnti-RB1CC1 Antibody Picoband®IHC analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). RB1CC1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1CC1 Antibody (A02414-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-ihc-testing-2.jpgAnti-RB1CC1 Antibody Picoband®IHC analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). RB1CC1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1CC1 Antibody (A02414-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-ihc-testing-3.jpgAnti-RB1CC1 Antibody Picoband®IHC analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). RB1CC1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1CC1 Antibody (A02414-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-ihc-testing-4.jpgAnti-RB1CC1 Antibody Picoband®IHC analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). RB1CC1 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1CC1 Antibody (A02414-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-ihc-testing-5.jpgAnti-RB1CC1 Antibody Picoband®IHC analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). RB1CC1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1CC1 Antibody (A02414-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-if-testing-1.jpgAnti-RB1CC1 Antibody Picoband®IF analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). RB1CC1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-RB1CC1 Antibody (A02414-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-if-testing-2.jpgAnti-RB1CC1 Antibody Picoband®IF analysis of RB1CC1 using anti-RB1CC1 antibody (A02414-1). RB1CC1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RB1CC1 Antibody (A02414-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02414-1-rb1cc1-primary-antibodies-fcm-testing-1.jpgAnti-RB1CC1 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-RB1CC1 antibody (A02414-1). Overlay histogram showing 293T cells stained with A02414-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RB1CC1 Antibody (A02414-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236632026-03-16T05:08:10+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236642026-03-13T05:04:58+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236652026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00241-4-histone-h2a.x-h2afx-primary-antibodies-wb-testing-1.jpgAnti-Histone H2A.X/H2AFX Antibody Western blot analysis of Histone H2A.X/H2AFX using anti-Histone H2A.X/H2AFX antibody (A00241-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse 3T3-L1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H2A.X/H2AFX antigen affinity purified polyclonal antibody (A00241-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H2A.X/H2AFX at approximately 17 kDa. The expected band size for Histone H2A.X/H2AFX is at 15 kDa. https://www.bosterbio.com/catalog/product/view/id/1236662026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00252-3-foxo3-primary-antibodies-wb-testing-1.jpgAnti-FOXO3A/FOXO3 AntibodyWestern blot analysis of FOXO3A/FOXO3 using anti-FOXO3A/FOXO3 antibody (A00252-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXO3A/FOXO3 antigen affinity purified polyclonal antibody (A00252-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOXO3A/FOXO3 at approximately 90 kDa. The expected band size for FOXO3A/FOXO3 is at 71 kDa. https://www.bosterbio.com/catalog/product/view/id/1236682026-03-17T05:14:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03036-2-xct-slc7a11-primary-antibodies-wb-testing-1.jpgAnti-xCT/SLC7A11 Antibody Picoband® Western blot analysis of xCT/SLC7A11 using anti-xCT/SLC7A11 antibody (A03036-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human U2OS whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-xCT/SLC7A11 antigen affinity purified polyclonal antibody (A03036-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for xCT/SLC7A11 at approximately 40-50 kDa. The expected band size for xCT/SLC7A11 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03036-2-slc7a11-primary-antibodies-ihc-testing-1.jpgAnti-xCT/SLC7A11 Antibody Picoband®IHC analysis of xCT/SLC7A11 using anti-xCT/SLC7A11 antibody (A03036-2). xCT/SLC7A11 was detected in a paraffin-embedded section of human ovraian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-xCT/SLC7A11 Antibody (A03036-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03036-2-12903_2025_6858_fig3_html.pngAnti-xCT/SLC7A11 Antibody Picoband®Expression patterns and diagnostic performance analysis. ( A ) Expression levels and ROC curve analysis of GSTA4, GGT6, SLC7A11, and CHAC1 in the GSE16134 dataset. ( B ) Validation of expression levels and ROC curve analysis in the GSE10334 dataset Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12903-025-06858-7'>41053677</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03036-2-12903_2025_6858_fig8_html.pngAnti-xCT/SLC7A11 Antibody Picoband®Validation of experimental periodontitis model. ( A ) HE staining showing periodontal tissue architecture in control and periodontitis groups. ( B ) Three-dimensional micro-CT reconstructions of maxillary molars. ( C ) Quantitative analysis of CEJ-ABC distance. ( D ) Immunohistochemical staining of SLC7A11. ( E ) Quantitative analysis of SLC7A11 immunohistochemical intensity. with * indicating statistical significance (** p < 0.01, *** p < 0.001). Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12903-025-06858-7'>41053677</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03036-2-xct-slc7a11-primary-antibodies-wb-testing-2.pngAnti-xCT/SLC7A11 Antibody Picoband®Western blot analysis of xCT/SLC7A11 using anti-xCT/SLC7A11 antibody (A03036-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1-5: model group-human uterine tissue lysates, Lane 6-10: young group-human uterine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-xCT/SLC7A11 antigen affinity purified polyclonal antibody (A03036-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1. hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate with Tanon 5200 system. A specific band was detected for xCT/SLC7A11 at approximately 40-50 kDa. The expected band size for xCT/SLC7A11 is at 40-50 kDa. https://www.bosterbio.com/catalog/product/view/id/1236692026-03-16T05:08:10+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236702026-03-16T05:08:10+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236712026-03-17T05:14:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00881-3-setdb1-primary-antibodies-wb-testing-1.jpgAnti-SETDB1 Antibody Picoband®Western blot analysis of SETDB1 using anti-SETDB1 antibody (A00881-3). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SETDB1 antigen affinity purified polyclonal antibody (A00881-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SETDB1 at approximately 180 kDa. The expected band size for SETDB1 is at 143 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00881-3-setdb1-primary-antibodies-fcm-testing-1.jpgAnti-SETDB1 Antibody Picoband®Flow Cytometry analysis of HeLa cells using anti-SETDB1 antibody (A00881-3). Overlay histogram showing HeLa cells stained with A00881-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SETDB1 Antibody (A00881-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236722026-03-16T05:08:10+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236732026-03-17T05:14:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07253-ift20-primary-antibodies-wb-testing-1.jpgAnti-IFT20 Antibody Picoband®Western blot analysis of IFT20 using anti-IFT20 antibody (A07253). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFT20 antigen affinity purified polyclonal antibody (A07253) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IFT20 at approximately 15 kDa. The expected band size for IFT20 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07253-ift20-primary-antibodies-ihc-testing-1.jpgAnti-IFT20 Antibody Picoband®IHC analysis of IFT20 using anti-IFT20 antibody (A07253). IFT20 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT20 Antibody (A07253) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07253-ift20-primary-antibodies-ihc-testing-2.jpgAnti-IFT20 Antibody Picoband®IHC analysis of IFT20 using anti-IFT20 antibody (A07253). IFT20 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT20 Antibody (A07253) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07253-ift20-primary-antibodies-ihc-testing-3.jpgAnti-IFT20 Antibody Picoband®IHC analysis of IFT20 using anti-IFT20 antibody (A07253). IFT20 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT20 Antibody (A07253) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07253-ift20-primary-antibodies-if-testing-1.jpgAnti-IFT20 Antibody Picoband®IF analysis of IFT20 using anti-IFT20 antibody (A07253). IFT20 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-IFT20 Antibody (A07253) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07253-ift20-primary-antibodies-fcm-testing-1.jpgAnti-IFT20 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-IFT20 antibody (A07253). Overlay histogram showing 293T cells stained with A07253 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFT20 Antibody (A07253, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236742026-03-16T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31546-smcr7l-mid51-mief1-primary-antibodies-wb-testing-1.jpgAnti-SMCR7L/MID51/MIEF1 Antibody Western blot analysis of SMCR7L/MID51/MIEF1 using anti-SMCR7L/MID51/MIEF1 antibody (A31546). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HT-1080 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat RH-35 whole cell lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMCR7L/MID51/MIEF1 antigen affinity purified polyclonal antibody (A31546) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SMCR7L/MID51/MIEF1 at approximately 48 kDa. The expected band size for SMCR7L/MID51/MIEF1 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31546-smcr7l-mid51-mief1-primary-antibodies-if-testing-1.jpgAnti-SMCR7L/MID51/MIEF1 AntibodyIF analysis of SMCR7L/MID51/MIEF1 using anti-SMCR7L/MID51/MIEF1 antibody (A31546). SMCR7L/MID51/MIEF1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-SMCR7L/MID51/MIEF1 Antibody (A31546) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1236752026-03-13T05:04:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01883-2-nmdar2b-grin2b-primary-antibodies-wb-testing-1.jpgAnti-NMDAR2B/GRIN2B Antibody Western blot analysis of NMDAR2B/GRIN2B using anti-NMDAR2B/GRIN2B antibody (A01883-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NMDAR2B/GRIN2B antigen affinity purified polyclonal antibody (A01883-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NMDAR2B/GRIN2B at approximately 180 kDa. The expected band size for NMDAR2B/GRIN2B is at 166 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01883-2-nmdar2b-grin2b-primary-antibodies-ihc-testing-1.jpgAnti-NMDAR2B/GRIN2B AntibodyIHC analysis of NMDAR2B/GRIN2B using anti-NMDAR2B/GRIN2B antibody (A01883-2). NMDAR2B/GRIN2B was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NMDAR2B/GRIN2B Antibody (A01883-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01883-2-nmdar2b-grin2b-primary-antibodies-ihc-testing-2.jpgAnti-NMDAR2B/GRIN2B AntibodyIHC analysis of NMDAR2B/GRIN2B using anti-NMDAR2B/GRIN2B antibody (A01883-2). NMDAR2B/GRIN2B was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NMDAR2B/GRIN2B Antibody (A01883-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01883-2-nmdar2b-grin2b-primary-antibodies-ihc-testing-3.jpgAnti-NMDAR2B/GRIN2B AntibodyIHC analysis of NMDAR2B/GRIN2B using anti-NMDAR2B/GRIN2B antibody (A01883-2). NMDAR2B/GRIN2B was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NMDAR2B/GRIN2B Antibody (A01883-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01883-2-nmdar2b-grin2b-primary-antibodies-ihc-testing-4.jpgAnti-NMDAR2B/GRIN2B AntibodyIHC analysis of NMDAR2B/GRIN2B using anti-NMDAR2B/GRIN2B antibody (A01883-2). NMDAR2B/GRIN2B was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NMDAR2B/GRIN2B Antibody (A01883-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1236762026-03-13T05:04:58+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236772026-03-17T05:14:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02418-1-eif2a-primary-antibodies-wb-testing-1.jpgAnti-EIF2A Antibody Picoband®Western blot analysis of EIF2A using anti-EIF2A antibody (A02418-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat PC-12 tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF2A antigen affinity purified polyclonal antibody (A02418-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EIF2A at approximately 65 kDa. The expected band size for EIF2A is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02418-1-eif2a-primary-antibodies-ihc-testing-1.jpgAnti-EIF2A Antibody Picoband®IHC analysis of EIF2A using anti-EIF2A antibody (A02418-1). EIF2A was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF2A Antibody (A02418-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02418-1-eif2a-primary-antibodies-fcm-testing-1.jpgAnti-EIF2A Antibody Picoband®Flow Cytometry analysis of Caco-2 cells using anti-EIF2A antibody (A02418-1). Overlay histogram showing Caco-2 cells stained with A02418-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-EIF2A Antibody (A02418-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236782026-04-02T05:00:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-hur-elavl1-primary-antibodies-wb-testing-1.jpgAnti-HuR/ELAVL1 Antibody Picoband® Western blot analysis of HuR/ELAVL1 using anti-HuR/ELAVL1 antibody (A00736-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HuR/ELAVL1 antigen affinity purified polyclonal antibody (A00736-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HuR/ELAVL1 at approximately 36 kDa. The expected band size for HuR/ELAVL1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-hur-elavl1-primary-antibodies-ihc-testing-2.jpgAnti-HuR/ELAVL1 Antibody Picoband® IHC analysis of HuR/ELAVL1 using anti-HuR/ELAVL1 antibody (A00736-1). HuR/ELAVL1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HuR/ELAVL1 Antibody (A00736-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-hur-elavl1-primary-antibodies-ihc-testing-3.jpgAnti-HuR/ELAVL1 Antibody Picoband® IHC analysis of HuR/ELAVL1 using anti-HuR/ELAVL1 antibody (A00736-1). HuR/ELAVL1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HuR/ELAVL1 Antibody (A00736-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-hur-elavl1-primary-antibodies-ihc-testing-4.jpgAnti-HuR/ELAVL1 Antibody Picoband® IHC analysis of HuR/ELAVL1 using anti-HuR/ELAVL1 antibody (A00736-1). HuR/ELAVL1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HuR/ELAVL1 Antibody (A00736-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-hur-elavl1-primary-antibodies-ihc-testing-5.jpgAnti-HuR/ELAVL1 Antibody Picoband® IHC analysis of HuR/ELAVL1 using anti-HuR/ELAVL1 antibody (A00736-1). HuR/ELAVL1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HuR/ELAVL1 Antibody (A00736-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-elavl1-primary-antibodies-wb-testing-1.jpgAnti-HuR/ELAVL1 Antibody Picoband®Western blot analysis of HuR/ELAVL1 using anti-HuR/ELAVL1 antibody (A00736-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HuR/ELAVL1 antigen affinity purified polyclonal antibody (A00736-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HuR/ELAVL1 at approximately 36 kDa. The expected band size for HuR/ELAVL1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-elavl1-primary-antibodies-if-testing-1.jpgAnti-HuR/ELAVL1 Antibody Picoband®IF analysis of HuR/ELAVL1 using anti-HuR/ELAVL1 antibody (A00736-1) and anti-Alpha Tubulin antibody (M03989-3). HuR/ELAVL1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HuR/ELAVL1 Antibody (A00736-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-elavl1-primary-antibodies-fcm-testing-1.jpgAnti-HuR/ELAVL1 Antibody Picoband®Flow Cytometry analysis of A431 cells using anti-HuR/ELAVL1 antibody (A00736-1). Overlay histogram showing A431 cells stained with A00736-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HuR/ELAVL1 Antibody (A00736-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00736-1-elavl1-primary-antibodies-fcm-testing-2.jpgAnti-HuR/ELAVL1 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-HuR/ELAVL1 antibody (A00736-1). Overlay histogram showing Jurkat cells stained with A00736-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HuR/ELAVL1 Antibody (A00736-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236792026-03-13T05:04:58+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236802026-03-13T05:04:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02292-1-nd1-mt-nd1-primary-antibodies-wb-testing-1.jpgAnti-ND1/MT-ND1 Antibody Western blot analysis of ND1/MT-ND1 using anti-ND1/MT-ND1 antibody (A02292-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat heart tissue lysates, Lane 3: mouse brain tissue lysates, Lane 4: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ND1/MT-ND1 antigen affinity purified polyclonal antibody (A02292-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ND1/MT-ND1 at approximately 36 kDa. The expected band size for ND1/MT-ND1 is at 36 kDa. https://www.bosterbio.com/catalog/product/view/id/1236812026-03-17T05:14:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04920-1-ndufs1-primary-antibodies-wb-testing-1_1.jpgAnti-NDUFS1 Antibody Picoband®Western blot analysis of NDUFS1 using anti-NDUFS1 antibody (A04920-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFS1 antigen affinity purified polyclonal antibody (A04920-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NDUFS1 at approximately 79 kDa. The expected band size for NDUFS1 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04920-1-ndufs1-primary-antibodies-wb-testing-1.jpgAnti-NDUFS1 Antibody Picoband® Western blot analysis of NDUFS1 using anti-NDUFS1 antibody (A04920-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat kidney tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse kidney tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFS1 antigen affinity purified polyclonal antibody (A04920-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NDUFS1 at approximately 79 kDa. The expected band size for NDUFS1 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04920-1-ndufs1-primary-antibodies-ihc-testing-1.jpgAnti-NDUFS1 Antibody Picoband®IHC analysis of NDUFS1 using anti-NDUFS1 antibody (A04920-1). NDUFS1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFS1 Antibody (A04920-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04920-1-ndufs1-primary-antibodies-ihc-testing-2.jpgAnti-NDUFS1 Antibody Picoband®IHC analysis of NDUFS1 using anti-NDUFS1 antibody (A04920-1). NDUFS1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFS1 Antibody (A04920-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04920-1-ndufs1-primary-antibodies-fcm-testing-1.jpgAnti-NDUFS1 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-NDUFS1 antibody (A04920-1). Overlay histogram showing HepG2 cells stained with A04920-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NDUFS1 Antibody (A04920-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236822026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07850-2-gorasp2-primary-antibodies-wb-testing-1.jpgAnti-GORASP2 AntibodyWestern blot analysis of GORASP2 using anti-GORASP2 antibody (A07850-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human COLO-320 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat PC-12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GORASP2 antigen affinity purified polyclonal antibody (A07850-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GORASP2 at approximately 59 kDa. The expected band size for GORASP2 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07850-2-gorasp2-primary-antibodies-ihc-testing-2.jpgAnti-GORASP2 AntibodyIHC analysis of GORASP2 using anti-GORASP2 antibody (A07850-2). GORASP2 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GORASP2 Antibody (A07850-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07850-2-gorasp2-primary-antibodies-ihc-testing-3.jpgAnti-GORASP2 AntibodyIHC analysis of GORASP2 using anti-GORASP2 antibody (A07850-2). GORASP2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GORASP2 Antibody (A07850-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07850-2-gorasp2-primary-antibodies-ihc-testing-1.jpgAnti-GORASP2 AntibodyIHC analysis of GORASP2 using anti-GORASP2 antibody (A07850-2). GORASP2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GORASP2 Antibody (A07850-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07850-2-gorasp2-primary-antibodies-if-testing-1.jpgAnti-GORASP2 AntibodyIF analysis of GORASP2 using anti-GORASP2 antibody (A07850-2) and anti-Tubulin Alpha antibody (M03989-3). GORASP2 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-GORASP2 Antibody (A07850-2) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07850-2-gorasp2-primary-antibodies-if-testing-2.jpgAnti-GORASP2 AntibodyIF analysis of GORASP2 using anti-GORASP2 antibody (A07850-2) and anti-Tubulin Alpha antibody (M03989-3). GORASP2 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-GORASP2 Antibody (A07850-2) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and Fluoro488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1236832026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03012-1-yme1l1-primary-antibodies-wb-testing-1.jpgAnti-YME1L1 Antibody Western blot analysis of YME1L1 using anti-YME1L1 antibody (A03012-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human COLO320 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YME1L1 antigen affinity purified polyclonal antibody (A03012-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for YME1L1 at approximately 63 kDa. The expected band size for YME1L1 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03012-1-yme1l1-primary-antibodies-ihc-testing-2.jpgAnti-YME1L1 Antibody IHC analysis of YME1L1 using anti-YME1L1 antibody (A03012-1). YME1L1 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-YME1L1 Antibody (A03012-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03012-1-yme1l1-primary-antibodies-ihc-testing-3.jpgAnti-YME1L1 Antibody IHC analysis of YME1L1 using anti-YME1L1 antibody (A03012-1). YME1L1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-YME1L1 Antibody (A03012-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03012-1-yme1l1-primary-antibodies-if-testing-1.jpgAnti-YME1L1 AntibodyIF analysis of YME1L1 using anti-YME1L1 antibody (A03012-1). YME1L1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-YME1L1 Antibody (A03012-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1236842026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00659-2-foxm1-primary-antibodies-wb-testing-1.jpgAnti-FOXM1 Antibody Picoband® Western blot analysis of FOXM1 using anti-FOXM1 antibody (A00659-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human DLD1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXM1 antigen affinity purified polyclonal antibody (A00659-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOXM1 at approximately 100-110 kDa. The expected band size for FOXM1 is at 84 kDa. https://www.bosterbio.com/catalog/product/view/id/1236852026-03-13T05:04:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02622-2-dmt1-slc11a2-primary-antibodies-wb-testing-1.jpgAnti-DMT1/SLC11A2 Antibody Western blot analysis of DMT1/SLC11A2 using anti-DMT1/SLC11A2 antibody (A02622-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat RH-35 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DMT1/SLC11A2 antigen affinity purified polyclonal antibody (A02622-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DMT1/SLC11A2 at approximately 70 kDa. The expected band size for DMT1/SLC11A2 is at 62 kDa. https://www.bosterbio.com/catalog/product/view/id/1236862026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236872026-03-13T05:04:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01432-3-krt14-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 14/KRT14 AntibodyWestern blot analysis of KRT14 using anti-KRT14 antibody (A01432-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT14 antigen affinity purified polyclonal antibody (A01432-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT14 at approximately 52 kDa. The expected band size for KRT14 is at 52 kDa. https://www.bosterbio.com/catalog/product/view/id/1236882026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06877-padi2-primary-antibodies-wb-testing-1.jpgAnti-PADI2 Antibody Picoband®Western blot analysis of PADI2 using anti-PADI2 antibody (A06877). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PADI2 antigen affinity purified polyclonal antibody (A06877) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PADI2 at approximately 75 kDa. The expected band size for PADI2 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06877-padi2-primary-antibodies-wb-testing-1_1.jpgAnti-PADI2 Antibody Picoband®Western blot analysis of PADI2 using anti-PADI2 antibody (A06877). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HL-60 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human THP-1 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat small intestine tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PADI2 antigen affinity purified polyclonal antibody (A06877) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PADI2 at approximately 75 kDa. The expected band size for PADI2 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06877-padi2-primary-antibodies-ihc-testing-1.jpgAnti-PADI2 Antibody Picoband®IHC analysis of PADI2 using anti-PADI2 antibody (A06877). PADI2 was detected in a paraffin-embedded section of human endometrial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PADI2 Antibody (A06877) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06877-padi2-primary-antibodies-ihc-testing-2.jpgAnti-PADI2 Antibody Picoband®IHC analysis of PADI2 using anti-PADI2 antibody (A06877). PADI2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PADI2 Antibody (A06877) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06877-padi2-primary-antibodies-ihc-testing-3.jpgAnti-PADI2 Antibody Picoband®IHC analysis of PADI2 using anti-PADI2 antibody (A06877). PADI2 was detected in a paraffin-embedded section of mouse spinal cord tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PADI2 Antibody (A06877) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06877-padi2-primary-antibodies-ihc-testing-4.jpgAnti-PADI2 Antibody Picoband®IHC analysis of PADI2 using anti-PADI2 antibody (A06877). PADI2 was detected in a paraffin-embedded section of rat spinal cord tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PADI2 Antibody (A06877) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06877-padi2-primary-antibodies-fcm-testing-1.jpgAnti-PADI2 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-PADI2 antibody (A06877). Overlay histogram showing MCF-7 cells stained with A06877 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PADI2 Antibody (A06877, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236892026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-wb-testing-1.jpgAnti-RB1 Antibody Picoband® Western blot analysis of RB1 using anti-RB1 antibody (A00039-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RB1 antigen affinity purified polyclonal antibody (A00039-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RB1 at approximately 110-120 kDa. The expected band size for RB1 is at 106 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-2.jpgAnti-RB1 Antibody Picoband® IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-3.jpgAnti-RB1 Antibody Picoband® IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-wb-testing-1_1.jpgAnti-RB1 Antibody Picoband®Western blot analysis of RB1 using anti-RB1 antibody (A00039-3). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RB1 antigen affinity purified polyclonal antibody (A00039-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RB1 at approximately 110 kDa. The expected band size for RB1 is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-1.jpgAnti-RB1 Antibody Picoband®IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-2_1.jpgAnti-RB1 Antibody Picoband®IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-3_1.jpgAnti-RB1 Antibody Picoband®IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-4.jpgAnti-RB1 Antibody Picoband®IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-5.jpgAnti-RB1 Antibody Picoband®IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-6.jpgAnti-RB1 Antibody Picoband®IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-ihc-testing-7.jpgAnti-RB1 Antibody Picoband®IHC analysis of RB1 using anti-RB1 antibody (A00039-3). RB1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RB1 Antibody (A00039-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-if-testing-1.jpgAnti-RB1 Antibody Picoband®IF analysis of RB1 using anti-RB1 antibody (A00039-3) and anti-Beta Tubulin antibody (M01857-3). RB1 was detected in an immunocytochemical section of SIHA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RB1 Antibody (A00039-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00039-3-rb1-primary-antibodies-fcm-testing-1.jpgAnti-RB1 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-RB1 antibody (A00039-3). Overlay histogram showing Jurkat cells stained with A00039-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RB1 Antibody (A00039-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236902026-03-16T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-1.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-2.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-3.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-4.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-5.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-6.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-7.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-8.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-9.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-10.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-ihc-testing-11.jpgAnti-CAPRIN1 AntibodyIHC analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). CAPRIN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CAPRIN1 Antibody (A05178-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05178-2-caprin1-primary-antibodies-wb-testing-1.jpgAnti-CAPRIN1 AntibodyWestern blot analysis of CAPRIN1 using anti-CAPRIN1 antibody (A05178-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAPRIN1 antigen affinity purified polyclonal antibody (A05178-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CAPRIN1 at approximately 116 kDa. The expected band size for CAPRIN1 is at 78 kDa. https://www.bosterbio.com/catalog/product/view/id/1236912026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14495-3-histone-h4-primary-antibodies-wb-testing-1.jpgAnti-Histone H4 Antibody Picoband®Western blot analysis of Histone H4 using anti-Histone H4 antibody (A14495-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human HT1080 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat thymus tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H4 antigen affinity purified polyclonal antibody (A14495-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H4 at approximately 14 kDa. The expected band size for Histone H4 is at 11 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14495-3-histone-h4-primary-antibodies-ihc-testing-1.jpgAnti-Histone H4 Antibody Picoband®IHC analysis of Histone H4 using anti-Histone H4 antibody (A14495-3). Histone H4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Histone H4 Antibody (A14495-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14495-3-histone-h4-primary-antibodies-if-testing-1.jpgAnti-Histone H4 Antibody Picoband®IF analysis of Histone H4 using anti-Histone H4 antibody (A14495-3). Histone H4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Histone H4 Antibody (A14495-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14495-3-histone-h4-primary-antibodies-if-testing-2.jpgAnti-Histone H4 Antibody Picoband®IF analysis of Histone H4 using anti-Histone H4 antibody (A14495-3) and anti-Beta Tubulin antibody (M01857-3). Histone H4 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Histone H4 Antibody (A14495-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14495-3-histone-h4-primary-antibodies-fcm-testing-1.jpgAnti-Histone H4 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-Histone H4 antibody (A14495-3). Overlay histogram showing 293T cells stained with A14495-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Histone H4 Antibody (A14495-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14495-3-histone-h4-primary-antibodies-fcm-testing-2.jpgAnti-Histone H4 Antibody Picoband®Flow Cytometry analysis of C6 cells using anti-Histone H4 antibody (A14495-3). Overlay histogram showing C6 cells stained with A14495-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Histone H4 Antibody (A14495-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14495-3-histone-h4-primary-antibodies-fcm-testing-3.jpgAnti-Histone H4 Antibody Picoband®Flow Cytometry analysis of HEPA1-6 cells using anti-Histone H4 antibody (A14495-3). Overlay histogram showing HEPA1-6 cells stained with A14495-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Histone H4 Antibody (A14495-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1236922026-03-16T05:08:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31589-tomm70-primary-antibodies-wb-testing-1.jpgAnti-TOM70/TOMM70 AntibodyWestern blot analysis of TOMM70 using anti-TOMM70 antibody (A31589). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human CACO-2 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TOMM70 antigen affinity purified polyclonal antibody (A31589) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TOMM70 at approximately 67 kDa. The expected band size for TOMM70 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31589-tomm70-primary-antibodies-ihc-testing-1.jpgAnti-TOM70/TOMM70 AntibodyIHC analysis of TOMM70 using anti-TOMM70 antibody (A31589). TOMM70 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TOMM70 Antibody (A31589) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31589-tomm70-primary-antibodies-ihc-testing-2.jpgAnti-TOM70/TOMM70 AntibodyIHC analysis of TOMM70 using anti-TOMM70 antibody (A31589). TOMM70 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TOMM70 Antibody (A31589) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1236932026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236942026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-wb-testing-1.jpgAnti-IGF2BP2 Antibody Picoband® Western blot analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGF2BP2 antigen affinity purified polyclonal antibody (A02010-4) at 0.5 μg/ml overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IGF2BP2 at approximately 66 kDa. The expected band size for IGF2BP2 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-2.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-3.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-4.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-5.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-6.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-7.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-8.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-ihc-testing-9.jpgAnti-IGF2BP2 Antibody Picoband® IHC analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02010-4-igf2bp2-primary-antibodies-if-testing-10.jpgAnti-IGF2BP2 Antibody Picoband® IF analysis of IGF2BP2 using anti-IGF2BP2 antibody (A02010-4). IGF2BP2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/ml rabbit anti-IGF2BP2 Antibody (A02010-4) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1236952026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236962026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03327-3-pex14-primary-antibodies-wb-testing-1.jpgAnti-PEX14 Antibody Picoband®Western blot analysis of PEX14 using anti-PEX14 antibody (A03327-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat PC-12 tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse NIH/3T3 tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PEX14 antigen affinity purified polyclonal antibody (A03327-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PEX14 at approximately 57 kDa. The expected band size for PEX14 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03327-3-pex14-primary-antibodies-ihc-testing-1.jpgAnti-PEX14 Antibody Picoband®IHC analysis of PEX14 using anti-PEX14 antibody (A03327-3). PEX14 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PEX14 Antibody (A03327-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03327-3-pex14-primary-antibodies-if-testing-1.jpgAnti-PEX14 Antibody Picoband®IF analysis of PEX14 using anti-PEX14 antibody (A03327-3). PEX14 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PEX14 Antibody (A03327-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1236972026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1236982026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04601-2-plod2-primary-antibodies-wb-testing-1.jpgAnti-PLOD2 Antibody Western blot analysis of PLOD2 using anti-PLOD2 antibody (A04601-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U87 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLOD2 antigen affinity purified polyclonal antibody (A04601-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PLOD2 at approximately 85 kDa. The expected band size for PLOD2 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04601-2-plod2-primary-antibodies-ihc-testing-2.jpgAnti-PLOD2 Antibody IHC analysis of PLOD2 using anti-PLOD2 antibody (A04601-2). PLOD2 was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PLOD2 Antibody (A04601-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1236992026-03-13T05:04:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00191-3-tet2-primary-antibodies-wb-testing-1.jpgAnti-TET2 AntibodyWestern blot analysis of TET2 using anti-TET2 antibody (A00191-3). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TET2 antigen affinity purified polyclonal antibody (A00191-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TET2 at approximately 250 kDa. The expected band size for TET2 is at 224 kDa. https://www.bosterbio.com/catalog/product/view/id/1237002026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06763-1-sqle-primary-antibodies-wb-testing-1.jpgAnti-SQLE Antibody Western blot analysis of SQLE using anti-SQLE antibody (A06763-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SQLE antigen affinity purified polyclonal antibody (A06763-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SQLE at approximately 64 kDa. The expected band size for SQLE is at 64 kDa. https://www.bosterbio.com/catalog/product/view/id/1237012026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237022026-04-02T05:00:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07937-1-uqcrc2-primary-antibodies-wb-testing-1.jpgAnti-UQCRC2 Antibody Picoband®Western blot analysis of UQCRC2 using anti-UQCRC2 antibody (A07937-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UQCRC2 antigen affinity purified polyclonal antibody (A07937-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UQCRC2 at approximately 48 kDa. The expected band size for UQCRC2 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07937-1-uqcrc2-primary-antibodies-wb-testing-1_1.jpgAnti-UQCRC2 Antibody Picoband®Western blot analysis of UQCRC2 using anti-UQCRC2 antibody (A07937-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UQCRC2 antigen affinity purified polyclonal antibody (A07937-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UQCRC2 at approximately 40 kDa. The expected band size for UQCRC2 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07937-1-uqcrc2-primary-antibodies-ihc-testing-1_1.jpgAnti-UQCRC2 Antibody Picoband®IHC analysis of UQCRC2 using anti-UQCRC2 antibody (A07937-1). UQCRC2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UQCRC2 Antibody (A07937-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07937-1-uqcrc2-primary-antibodies-ihc-testing-2_1.jpgAnti-UQCRC2 Antibody Picoband®IHC analysis of UQCRC2 using anti-UQCRC2 antibody (A07937-1). UQCRC2 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UQCRC2 Antibody (A07937-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07937-1-uqcrc2-primary-antibodies-fcm-testing-1.jpgAnti-UQCRC2 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-UQCRC2 antibody (A07937-1). Overlay histogram showing 293T cells stained with A07937-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-UQCRC2 Antibody (A07937-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07937-1-uqcrc2-primary-antibodies-ihc-testing-1.jpgAnti-UQCRC2 Antibody Picoband®IHC analysis of UQCRC2 using anti-UQCRC2 antibody (A07937-1). UQCRC2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-UQCRC2 Antibody (A07937-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07937-1-uqcrc2-primary-antibodies-ihc-testing-2.jpgAnti-UQCRC2 Antibody Picoband®IHC analysis of UQCRC2 using anti-UQCRC2 antibody (A07937-1). UQCRC2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-UQCRC2 Antibody (A07937-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237042026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237052026-04-03T05:00:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03059-2-dync1h1-primary-antibodies-ihc-testing-1.jpgAnti-DYNC1H1 AntibodyIHC analysis of DYNC1H1 using anti-DYNC1H1 antibody (A03059-2). DYNC1H1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNC1H1 Antibody (A03059-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03059-2-dync1h1-primary-antibodies-ihc-testing-2.jpgAnti-DYNC1H1 AntibodyIHC analysis of DYNC1H1 using anti-DYNC1H1 antibody (A03059-2). DYNC1H1 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DYNC1H1 Antibody (A03059-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237062026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237072026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03845-2-rab35-primary-antibodies-wb-testing-1.jpgAnti-RAB35 Antibody Picoband®Western blot analysis of RAB35 using anti-RAB35 antibody (A03845-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB35 antigen affinity purified polyclonal antibody (A03845-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RAB35 at approximately 23 kDa. The expected band size for RAB35 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03845-2-rab35-primary-antibodies-if-testing-1.jpgAnti-RAB35 Antibody Picoband®IF analysis of RAB35 using anti-RAB35 antibody (A03845-2). RAB35 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RAB35 Antibody (A03845-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03845-2-rab35-primary-antibodies-fcm-testing-1.jpgAnti-RAB35 Antibody Picoband®Flow Cytometry analysis of C6 cells using anti-RAB35 antibody (A03845-2). Overlay histogram showing C6 cells stained with A03845-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RAB35 Antibody (A03845-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03845-2-rab35-primary-antibodies-fcm-testing-2.jpgAnti-RAB35 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-RAB35 antibody (A03845-2). Overlay histogram showing MCF-7 cells stained with A03845-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RAB35 Antibody (A03845-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1237082026-03-13T05:04:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01934-2-kif5b-primary-antibodies-wb-testing-1.jpgAnti-KIF5B Antibody Western blot analysis of KIF5B using anti-KIF5B antibody (A01934-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse Neuro-2a whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KIF5B antigen affinity purified polyclonal antibody (A01934-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KIF5B at approximately 110 kDa. The expected band size for KIF5B is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01934-2-kif5b-primary-antibodies-ihc-testing-2.jpgAnti-KIF5B Antibody IHC analysis of KIF5B using anti-KIF5B antibody (A01934-2). KIF5B was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-KIF5B Antibody (A01934-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01934-2-kif5b-primary-antibodies-ihc-testing-3.jpgAnti-KIF5B Antibody IHC analysis of KIF5B using anti-KIF5B antibody (A01934-2). KIF5B was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-KIF5B Antibody (A01934-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237092026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237112026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237122026-03-17T05:14:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-wb-testing-1.jpgAnti-ADAM12 Antibody Picoband® Western blot analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM12 antigen affinity purified polyclonal antibody (A02264-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ADAM12 at approximately 75 kDa. The expected band size for ADAM12 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-ihc-testing-2.jpgAnti-ADAM12 Antibody Picoband® IHC analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). ADAM12 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ADAM12 Antibody (A02264-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-ihc-testing-3.jpgAnti-ADAM12 Antibody Picoband® IHC analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). ADAM12 was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ADAM12 Antibody (A02264-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-wb-testing-1_1.jpgAnti-ADAM12 Antibody Picoband®Western blot analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM12 antigen affinity purified polyclonal antibody (A02264-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ADAM12 at approximately 90 kDa. The expected band size for ADAM12 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-ihc-testing-1.jpgAnti-ADAM12 Antibody Picoband®IHC analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). ADAM12 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ADAM12 Antibody (A02264-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-ihc-testing-2_1.jpgAnti-ADAM12 Antibody Picoband®IHC analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). ADAM12 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ADAM12 Antibody (A02264-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-if-testing-1.jpgAnti-ADAM12 Antibody Picoband®IF analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). ADAM12 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ADAM12 Antibody (A02264-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-if-testing-2.jpgAnti-ADAM12 Antibody Picoband®IF analysis of ADAM12 using anti-ADAM12 antibody (A02264-2). ADAM12 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ADAM12 Antibody (A02264-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-fcm-testing-1.jpgAnti-ADAM12 Antibody Picoband®Flow Cytometry analysis of C6 cells using anti-ADAM12 antibody (A02264-2). Overlay histogram showing C6 cells stained with A02264-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ADAM12 Antibody (A02264-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02264-2-adam12-primary-antibodies-fcm-testing-2.jpgAnti-ADAM12 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-ADAM12 antibody (A02264-2). Overlay histogram showing MCF-7 cells stained with A02264-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ADAM12 Antibody (A02264-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1237132026-03-13T05:04:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00683-2-ire1-ern1-primary-antibodies-wb-testing-1.jpgAnti-IRE1/ERN1 Antibody Western blot analysis of IRE1/ERN1 using anti-IRE1/ERN1 antibody (A00683-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRE1/ERN1 antigen affinity purified polyclonal antibody (A00683-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IRE1/ERN1 at approximately 120 kDa. The expected band size for IRE1/ERN1 is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00683-2-ire1-ern1-primary-antibodies-ihc-testing-2.jpgAnti-IRE1/ERN1 Antibody IHC analysis of IRE1/ERN1 using anti-IRE1/ERN1 antibody (A00683-2). IRE1/ERN1 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IRE1/ERN1 Antibody (A00683-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00683-2-ire1-ern1-primary-antibodies-ihc-testing-3.jpgAnti-IRE1/ERN1 Antibody IHC analysis of IRE1/ERN1 using anti-IRE1/ERN1 antibody (A00683-2). IRE1/ERN1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IRE1/ERN1 Antibody (A00683-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00683-2-ire1-ern1-primary-antibodies-ihc-testing-4.jpgAnti-IRE1/ERN1 Antibody IHC analysis of IRE1/ERN1 using anti-IRE1/ERN1 antibody (A00683-2). IRE1/ERN1 was detected in a paraffin-embedded section of human non-small-cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IRE1/ERN1 Antibody (A00683-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00683-2-ire1-ern1-primary-antibodies-ihc-testing-5.jpgAnti-IRE1/ERN1 Antibody IHC analysis of IRE1/ERN1 using anti-IRE1/ERN1 antibody (A00683-2). IRE1/ERN1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IRE1/ERN1 Antibody (A00683-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00683-2-ire1-ern1-primary-antibodies-ihc-testing-6.jpgAnti-IRE1/ERN1 Antibody IHC analysis of IRE1/ERN1 using anti-IRE1/ERN1 antibody (A00683-2). IRE1/ERN1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IRE1/ERN1 Antibody (A00683-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00683-2-ire1-ern1-primary-antibodies-ihc-testing-7.jpgAnti-IRE1/ERN1 Antibody IHC analysis of IRE1/ERN1 using anti-IRE1/ERN1 antibody (A00683-2). IRE1/ERN1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IRE1/ERN1 Antibody (A00683-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237142026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237152026-04-03T05:00:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01388-4-trkb-ntrk2-primary-antibodies-wb-testing-1.jpgAnti-TrkB/NTRK2 Antibody Picoband® Western blot analysis of TrkB/NTRK2 using anti-TrkB/NTRK2 antibody (A01388-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TrkB/NTRK2 antigen affinity purified polyclonal antibody (A01388-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TrkB/NTRK2 at approximately 92150 kDa. The expected band size for TrkB/NTRK2 is at 92 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01388-4-trkb-ntrk2-primary-antibodies-ihc-testing-2.jpgAnti-TrkB/NTRK2 Antibody Picoband® IHC analysis of TrkB/NTRK2 using anti-TrkB/NTRK2 antibody (A01388-4). TrkB/NTRK2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TrkB/NTRK2 Antibody (A01388-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01388-4-trkb-ntrk2-primary-antibodies-ihc-testing-3.jpgAnti-TrkB/NTRK2 Antibody Picoband® IHC analysis of TrkB/NTRK2 using anti-TrkB/NTRK2 antibody (A01388-4). TrkB/NTRK2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TrkB/NTRK2 Antibody (A01388-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01388-4-41598_2018_27787_fig1_html.jpgAnti-TrkB/NTRK2 Antibody Picoband®The representative samples of immunohistochemical staining for AGE, RAGE, TGF-β1, TGF- β1 receptor, BDNF and TrkB in the colon wall of two groups. The microscopy with high magnification have been inserted in each single histological photo (arrow) in order to display the localization of markers. The staining of all proteins was stronger in the muscle layer than other layers. In the different layers, the staining of AGE, RAGE, TGF-β1 and TGF- β1 receptor was stronger whereas the staining of BDNF and TrkB was weaker in the Diabetes group than in Control group. Bar = 100 um. Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-27787-2'>29930382</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01388-4-41598_2018_27787_fig2_html.jpgAnti-TrkB/NTRK2 Antibody Picoband®The fraction of AGE, RAGE, TGF-β1, TGF- β1 receptor, BDNF and TrkB in the different layers of the colon between two groups. In the different layers, the fraction of AGE, RAGE, TGF-β1 and TGF- β1 receptor was bigger whereas the fraction of BDNF and TrkB was smaller in the Diabetes group than in Control group. Compared with Control group: *P < 0.05, **P < 0.01. Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-27787-2'>29930382</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01388-4-41598_2018_27787_fig4_html.jpgAnti-TrkB/NTRK2 Antibody Picoband®( A ) Correlation between AGE and RAGE in different layers; ( B ) Correlation between TGF-β1 and TGF-β1receptor in different layers; ( C ) Correlation between BDNF and TrkB in different layers; ( D ) Correlation between RAGE and TGF-β1receptor in different layers. Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-018-27787-2'>29930382</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01388-4-ntrk2-primary-antibodies-wb-testing-1.jpgAnti-TrkB/NTRK2 Antibody Picoband®Western blot analysis of TrkB/NTRK2 using anti-TrkB/NTRK2 antibody (A01388-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TrkB/NTRK2 antigen affinity purified polyclonal antibody (A01388-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TrkB/NTRK2 at approximately 92 kDa. The expected band size for TrkB/NTRK2 is at 92 kDa. https://www.bosterbio.com/catalog/product/view/id/1237162026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237172026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237182026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04964-2-ifitm2-primary-antibodies-ihc-testing-1.jpgAnti-IFITM2 Antibody IHC analysis of IFITM2 using anti-IFITM2 antibody (A04964-2). IFITM2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IFITM2 Antibody (A04964-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04964-2-ifitm2-primary-antibodies-ihc-testing-2.jpgAnti-IFITM2 Antibody IHC analysis of IFITM2 using anti-IFITM2 antibody (A04964-2). IFITM2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-IFITM2 Antibody (A04964-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237192026-03-13T05:04:59+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237202026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237212026-03-13T05:05:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02240-1-mct1-slc16a1-primary-antibodies-wb-testing-1.jpgAnti-MCT1/SLC16A1 Antibody Western blot analysis of MCT1/SLC16A1 using anti-MCT1/SLC16A1 antibody (A02240-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U87 whole cell lysates, Lane 2: human HL-60 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCT1/SLC16A1 antigen affinity purified polyclonal antibody (A02240-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MCT1/SLC16A1 at approximately 40 kDa. The expected band size for MCT1/SLC16A1 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02240-1-mct1-slc16a1-primary-antibodies-ihc-testing-2.jpgAnti-MCT1/SLC16A1 Antibody IHC analysis of MCT1/SLC16A1 using anti-MCT1/SLC16A1 antibody (A02240-1). MCT1/SLC16A1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MCT1/SLC16A1 Antibody (A02240-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02240-1-mct1-slc16a1-primary-antibodies-ihc-testing-3.jpgAnti-MCT1/SLC16A1 Antibody IHC analysis of MCT1/SLC16A1 using anti-MCT1/SLC16A1 antibody (A02240-1). MCT1/SLC16A1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MCT1/SLC16A1 Antibody (A02240-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237222026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05510-2-mct4-slc16a3-primary-antibodies-wb-testing-1.jpgAnti-MCT4/SLC16A3 Antibody Western blot analysis of MCT4/SLC16A3 using anti-MCT4/SLC16A3 antibody (A05510-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCT4/SLC16A3 antigen affinity purified polyclonal antibody (A05510-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MCT4/SLC16A3 at approximately 40 kDa. The expected band size for MCT4/SLC16A3 is at 49 kDa. https://www.bosterbio.com/catalog/product/view/id/1237232026-03-13T05:05:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03534-2-nbr1-primary-antibodies-ihc-testing-1.jpgAnti-NBR1 AntibodyIHC analysis of NBR1 using anti-NBR1 antibody (A03534-2). NBR1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NBR1 Antibody (A03534-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03534-2-nbr1-primary-antibodies-ihc-testing-2.jpgAnti-NBR1 AntibodyIHC analysis of NBR1 using anti-NBR1 antibody (A03534-2). NBR1 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NBR1 Antibody (A03534-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237242026-03-13T05:05:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-wb-testing-1.jpgAnti-PDH E1 Alpha/PDHA1 Antibody Western blot analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDH E1 Alpha/PDHA1 antigen affinity purified polyclonal antibody (A01906-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDH E1 Alpha/PDHA1 at approximately 40 kDa. The expected band size for PDH E1 Alpha/PDHA1 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-ihc-testing-6.jpgAnti-PDH E1 Alpha/PDHA1 Antibody IHC analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). PDH E1 Alpha/PDHA1 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PDH E1 Alpha/PDHA1 Antibody (A01906-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-ihc-testing-7.jpgAnti-PDH E1 Alpha/PDHA1 Antibody IHC analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). PDH E1 Alpha/PDHA1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PDH E1 Alpha/PDHA1 Antibody (A01906-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-ihc-testing-5.jpgAnti-PDH E1 Alpha/PDHA1 Antibody IHC analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). PDH E1 Alpha/PDHA1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PDH E1 Alpha/PDHA1 Antibody (A01906-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-ihc-testing-4.jpgAnti-PDH E1 Alpha/PDHA1 Antibody IHC analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). PDH E1 Alpha/PDHA1 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PDH E1 Alpha/PDHA1 Antibody (A01906-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-ihc-testing-3.jpgAnti-PDH E1 Alpha/PDHA1 Antibody IHC analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). PDH E1 Alpha/PDHA1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PDH E1 Alpha/PDHA1 Antibody (A01906-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-ihc-testing-2.jpgAnti-PDH E1 Alpha/PDHA1 Antibody IHC analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). PDH E1 Alpha/PDHA1 was detected in a paraffin-embedded section of human appendix carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PDH E1 Alpha/PDHA1 Antibody (A01906-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdha1-primary-antibodies-if-testing-1.jpgAnti-PDH E1 Alpha/PDHA1 AntibodyIF analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4). PDH E1 Alpha/PDHA1 was detected in an immunocytochemical section of chuman Hela ells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-PDH E1 Alpha/PDHA1 Antibody (A01906-4) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01906-4-pdh-e1-alpha-pdha1-primary-antibodies-ip-testing-1.jpgAnti-PDH E1 Alpha/PDHA1 AntibodyImmunoprecipitating (IP) PDH E1 Alpha/PDHA1 in HepG2 whole cell lysate. Western blot analysis of PDH E1 Alpha/PDHA1 using anti-PDH E1 Alpha/PDHA1 antibody (A01906-4); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-PDH E1 Alpha/PDHA1 antibody in HepG2 whole cell lysate; Lane 3: anti-PDH E1 Alpha/PDHA1 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PDH E1 Alpha/PDHA1 antigen affinity purified polyclonal antibody (A01906-4) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light Chiain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PDH E1 Alpha/PDHA1 at approximately 40 kDa. The expected band size for PDH E1 Alpha/PDHA1 is at 43 kDa. https://www.bosterbio.com/catalog/product/view/id/1237252026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237262026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237272026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06465-1-mthfd2-primary-antibodies-wb-testing-1.jpgAnti-MTHFD2 Antibody Western blot analysis of MTHFD2 using anti-MTHFD2 antibody (A06465-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTHFD2 antigen affinity purified polyclonal antibody (A06465-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MTHFD2 at approximately 35 kDa. The expected band size for MTHFD2 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06465-1-mthfd2-primary-antibodies-ihc-testing-2.jpgAnti-MTHFD2 Antibody IHC analysis of MTHFD2 using anti-MTHFD2 antibody (A06465-1). MTHFD2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTHFD2 Antibody (A06465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06465-1-mthfd2-primary-antibodies-ihc-testing-3.jpgAnti-MTHFD2 Antibody IHC analysis of MTHFD2 using anti-MTHFD2 antibody (A06465-1). MTHFD2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTHFD2 Antibody (A06465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06465-1-mthfd2-primary-antibodies-ihc-testing-4.jpgAnti-MTHFD2 Antibody IHC analysis of MTHFD2 using anti-MTHFD2 antibody (A06465-1). MTHFD2 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTHFD2 Antibody (A06465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06465-1-mthfd2-primary-antibodies-ihc-testing-5.jpgAnti-MTHFD2 Antibody IHC analysis of MTHFD2 using anti-MTHFD2 antibody (A06465-1). MTHFD2 was detected in a paraffin-embedded section of mouse epididymis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTHFD2 Antibody (A06465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06465-1-mthfd2-primary-antibodies-ihc-testing-6.jpgAnti-MTHFD2 Antibody IHC analysis of MTHFD2 using anti-MTHFD2 antibody (A06465-1). MTHFD2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTHFD2 Antibody (A06465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237282026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237292026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07110-1-gbp5-primary-antibodies-wb-testing-1.jpgAnti-GBP5 AntibodyWestern blot analysis of GBP5 using anti-GBP5 antibody (A07110-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human U937 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: mouse spleen tissue lysates, Lane 5: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GBP5 antigen affinity purified polyclonal antibody (A07110-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GBP5 at approximately 67 kDa. The expected band size for GBP5 is at 67 kDa. https://www.bosterbio.com/catalog/product/view/id/1237302026-03-13T05:05:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00436-3-hmga2-primary-antibodies-wb-testing-1.jpgAnti-HMGA2 Antibody Western blot analysis of HMGA2 using anti-HMGA2 antibody (A00436-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HMGA2 antigen affinity purified polyclonal antibody (A00436-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HMGA2 at approximately 18-20 kDa. The expected band size for HMGA2 is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00436-3-hmga2-primary-antibodies-ihc-testing-2.jpgAnti-HMGA2 Antibody IHC analysis of HMGA2 using anti-HMGA2 antibody (A00436-3). HMGA2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HMGA2 Antibody (A00436-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00436-3-hmga2-primary-antibodies-if-testing-3.jpgAnti-HMGA2 Antibody IF analysis of HMGA2 using anti-HMGA2 antibody (A00436-3). HMGA2 was detected in an immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-HMGA2 Antibody (A00436-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1237312026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1237322026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07895-2-cox5a-primary-antibodies-wb-testing-1.jpgAnti-COX5A Antibody Western blot analysis of COX5A using anti-COX5A antibody (A07895-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COX5A antigen affinity purified polyclonal antibody (A07895-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for COX5A at approximately 15 kDa. The expected band size for COX5A is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07895-2-cox5a-primary-antibodies-ihc-testing-2.jpgAnti-COX5A Antibody IHC analysis of COX5A using anti-COX5A antibody (A07895-2). COX5A was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-COX5A Antibody (A07895-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07895-2-cox5a-primary-antibodies-ihc-testing-3.jpgAnti-COX5A Antibody IHC analysis of COX5A using anti-COX5A antibody (A07895-2). COX5A was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-COX5A Antibody (A07895-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07895-2-cox5a-primary-antibodies-ihc-testing-4.jpgAnti-COX5A Antibody IHC analysis of COX5A using anti-COX5A antibody (A07895-2). COX5A was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-COX5A Antibody (A07895-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1237332026-03-17T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-ihc-testing-6.jpgAnti-INF2 Antibody Picoband®IHC analysis of INF2 using anti-INF2 antibody (A02710-2). INF2 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INF2 Antibody (A02710-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-wb-testing-1_1.jpgAnti-INF2 Antibody Picoband® Western blot analysis of INF2 using anti-INF2 antibody (A02710-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INF2 antigen affinity purified polyclonal antibody (A02710-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for INF2 at approximately 180 kDa. The expected band size for INF2 is at 136 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-ihc-testing-2.jpgAnti-INF2 Antibody Picoband® IHC analysis of INF2 using anti-INF2 antibody (A02710-2). INF2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INF2 Antibody (A02710-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-ihc-testing-3.jpgAnti-INF2 Antibody Picoband® IHC analysis of INF2 using anti-INF2 antibody (A02710-2). INF2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INF2 Antibody (A02710-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-ihc-testing-4.jpgAnti-INF2 Antibody Picoband® IHC analysis of INF2 using anti-INF2 antibody (A02710-2). INF2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INF2 Antibody (A02710-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-ihc-testing-5.jpgAnti-INF2 Antibody Picoband® IHC analysis of INF2 using anti-INF2 antibody (A02710-2). INF2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INF2 Antibody (A02710-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-if-testing-6.jpgAnti-INF2 Antibody Picoband® IF analysis of INF2 using anti-INF2 antibody (A02710-2). INF2 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/ml rabbit anti-INF2 Antibody (A02710-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02710-2-inf2-primary-antibodies-ip-testing-7.jpgAnti-INF2 Antibody Picoband® Immunoprecipitating (IP) INF2 in Hela whole cell lysate. Western blot analysis of INF2 using anti-INF2 antibody (A02710-2); Lane 1: Hela whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-INF2 antibody in Hela whole cell lysate; Lane 3: anti-INF2 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-INF2 antigen affinity purified polyclonal antibody (A02710-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for INF2 at approximately 180 kDa. The expected band size for INF2 is at 136 kDa. https://www.bosterbio.com/catalog/product/view/id/1237342026-03-10T04:35:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2244.pngHuman Layilin ELISA Kit PicoKine®Human Layilin PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1237362026-03-10T04:35:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2246.pngHuman ASAHL ELISA Kit PicoKine®Human ASAHL PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1237382026-03-10T04:35:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2248.pngHuman NAGA ELISA Kit PicoKine®Human NAGA PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1237392026-03-10T04:35:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2249.pngHuman Napsin A ELISA Kit PicoKine®Human Napsin A PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1237402026-03-10T04:35:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2250.jpgHuman NCR2 ELISA Kit PicoKine®Human NCR2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1237412026-03-10T04:35:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2251.pngHuman PDGFRB ELISA Kit PicoKine®Human PDGFRB PicoKine ELISA Kit standard curve https://www.bosterbio.com/products/ez-set-elisa-kits-antibody-pairs/human-vegf-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0539-boster.html2026-03-10T04:35:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0539.pngHuman VEGF ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human VEGF EZ Set ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-torulopsis-glabrata-pdr1-antibody-dz41406-boster.html2026-03-10T04:35:43+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-african-clawed-frog-plekhg5-antibody-dz41390-boster.html2026-03-10T04:35:43+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-mouse-ear-cress-nup1-nup136-antibody-dz41396-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-mouse-ear-cress-aladin-antibody-dz41397-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-dhd-antibody-dz41398-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-cg12942-antibody-dz41399-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-burkholderia-glumae-qsmr-antibody-dz41401-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-austrofundulus-limnaeus-g3bp1-antibody-dz41405-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-lrrk-antibody-dz41384-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-venom-pla2-antibody-dz41404-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-spire-antibody-dz41407-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-mylpfa-mutant-antibody-dz41409-boster.html2026-03-17T05:14:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-unc13a-antibody-dz41411-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-fife-antibody-dz41412-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-rim-antibody-dz41413-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-liprin-alpha-antibody-dz41414-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-saccharomyces-cerevisiae-elp1-antibody-dz41402-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-unc45b-antibody-dz41410-boster.html2026-03-17T05:14:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-wtpre-ppifb-antibody-dz41415-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-xenous-laevis-folr1-l-antibody-dz41423-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-pea-polyphenol-oxidase-ppo-antibody-dz41424-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-squid-adar1-antibody-dz41418-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-cdk9-55-antibody-dz41422-boster.html2026-03-10T04:35:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-nfix-picoband-trade-antibody-a04138-1-boster.html2026-03-17T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04138-1-nfix-primary-antibodies-wb-testing-1.jpgAnti-NFIX Antibody Picoband® Western blot analysis of NFIX using anti-NFIX antibody (A04138-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFIX antigen affinity purified polyclonal antibody (Catalog # A04138-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NFIX at approximately 55 kDa. The expected band size for NFIX is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04138-1-nfix-primary-antibodies-if-testing-2.jpgAnti-NFIX Antibody Picoband® IF analysis of NFIX using anti-NFIX antibody (A04138-1). NFIX was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NFIX Antibody (A04138-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04138-1-nfix-primary-antibodies-fcm-testing-3.pngAnti-NFIX Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-NFIX antibody (A04138-1). Overlay histogram showing U20S cells stained with A04138-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFIX Antibody (A04138-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nfkbiz-picoband-trade-antibody-a05312-1-boster.html2026-03-17T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05312-1-nfkbiz-primary-antibodies-wb-testing-1.jpgAnti-NFKBIZ Antibody Picoband® Western blot analysis of NFKBIZ using anti-NFKBIZ antibody (A05312-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFKBIZ antigen affinity purified polyclonal antibody (Catalog # A05312-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NFKBIZ at approximately 85 kDa. The expected band size for NFKBIZ is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05312-1-nfkbiz-primary-antibodies-if-testing-2.jpgAnti-NFKBIZ Antibody Picoband® IF analysis of NFKBIZ using anti-NFKBIZ antibody (A05312-1) and anti-Beta Tubulin antibody (M01857-3). NFKBIZ was detected in immunocytochemical section of SIHA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NFKBIZ Antibody (A05312-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05312-1-nfkbiz-primary-antibodies-fcm-testing-3.pngAnti-NFKBIZ Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NFKBIZ antibody (A05312-1). Overlay histogram showing HEL cells stained with A05312-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFKBIZ Antibody (A05312-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nhp2-picoband-trade-antibody-a05665-1-boster.html2026-03-17T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05665-1-nhp2-primary-antibodies-wb-testing-1_1.jpgAnti-NHP2 Antibody Picoband® Western blot analysis of NHP2 using anti-NHP2 antibody (A04887-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NHP2 antigen affinity purified polyclonal antibody (A04887-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NHP2 at approximately 20 kDa. The expected band size for NHP2 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05665-1-nhp2-primary-antibodies-if-testing-2_1.jpgAnti-NHP2 Antibody Picoband® IF analysis of NHP2 using anti-NHP2 antibody (A05665-1) and anti-Beta Tubulin antibody (M01857-3). NHP2 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NHP2 Antibody (A05665-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05665-1-nhp2-primary-antibodies-ip-testing-3.jpgAnti-NHP2 Antibody Picoband® Immunoprecipitating NHP2 in SH-SY5Y whole cell lysate. Western blot analysis of NHP2 using anti-NHP2 antibody (A05665-1); Lane 1: SH-SY5Y whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-NHP2 antibody in SH-SY5Y whole cell lysate; Lane 3: anti-NHP2 antibody (2μg) + SH-SY5Y whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NHP2 antigen affinity purified polyclonal antibody (A05665-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NHP2 at approximately 20 kDa. The expected band size for NHP2 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05665-1-nhp2-primary-antibodies-fcm-testing-4.jpgAnti-NHP2 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-NHP2 antibody (A05665-1). Overlay histogram showing CACO-2 cells stained with A05665-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NHP2 Antibody (A05665-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-ninein-nin-picoband-trade-antibody-a03001-1-boster.html2026-03-17T05:14:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03001-1-nin-primary-antibodies-wb-testing-1.jpgAnti-Ninein/NIN Antibody Picoband® Western blot analysis of Ninein/NIN using anti-Ninein/NIN antibody (A03001-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MOLT4 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ninein/NIN antigen affinity purified polyclonal antibody (Catalog # A03001-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Ninein/NIN at approximately 260 kDa. The expected band size for Ninein/NIN is at 243 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03001-1-nin-primary-antibodies-fcm-testing-2.pngAnti-Ninein/NIN Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-Ninein/NIN antibody (A03001-1). Overlay histogram showing MCF-7 cells stained with A03001-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Ninein/NIN Antibody (A03001-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nlrp9-picoband-trade-antibody-a14119-1-boster.html2026-03-17T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14119-1-nlrp9-primary-antibodies-wb-testing-1.jpgAnti-NLRP9 Antibody Picoband® Western blot analysis of NLRP9 using anti-NLRP9 antibody (A14119-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NLRP9 antigen affinity purified polyclonal antibody (Catalog # A14119-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NLRP9 at approximately 113 kDa. The expected band size for NLRP9 is at 113 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-caspase-1-p20-casp1-picoband-trade-antibody-a00048-1-boster.html2026-03-17T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00048-1-casp1-primary-antibodies-wb-testing-1.jpgAnti-Caspase 1(p20)/CASP1 Antibody Picoband® Western blot analysis of Caspase 1(P20)/CASP1 using anti-Caspase 1(P20)/CASP1 antibody (A00048-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-2 whole cell lysates, Lane 2: human U937 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Caspase 1(P20)/CASP1 antigen affinity purified polyclonal antibody (Catalog # A00048-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Caspase 1(P20)/CASP1 at approximately 47 kDa. The expected band size for Caspase 1(P20)/CASP1 is at 47 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-tp53bp1-picoband-trade-antibody-a00397-1-boster.html2026-03-17T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00397-1-tp53bp1-primary-antibodies-wb-testing-1.jpgAnti-TP53BP1 Antibody Picoband® Western blot analysis of TP53BP1 using anti-TP53BP1 antibody (A00397-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TP53BP1 antigen affinity purified polyclonal antibody (Catalog # A00397-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TP53BP1 at approximately 300-350 kDa. The expected band size for TP53BP1 is at 210 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00397-1-tp53bp1-primary-antibodies-ihc-testing-1.jpgAnti-TP53BP1 Antibody Picoband®IHC analysis of TP53BP1 using anti-TP53BP1 antibody (A00397-1). TP53BP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TP53BP1 Antibody (A00397-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00397-1-tp53bp1-primary-antibodies-if-testing-2.jpgAnti-TP53BP1 Antibody Picoband® IF analysis of TP53BP1 using anti-TP53BP1 antibody (A00397-1) and anti-Beta Tubulin antibody (M01857-3). TP53BP1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TP53BP1 Antibody (A00397-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00397-1-tp53bp1-primary-antibodies-fcm-testing-3.pngAnti-TP53BP1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-TP53BP1 antibody (A00397-1). Overlay histogram showing HepG2 cells stained with A00397-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TP53BP1 Antibody (A00397-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-six4-picoband-trade-antibody-a05695-1-boster.html2026-03-17T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05695-1-six4-primary-antibodies-wb-testing-1.jpgAnti-SIX4 Antibody Picoband® Western blot analysis of SIX4 using anti-SIX4 antibody (A05695-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIX4 antigen affinity purified polyclonal antibody (Catalog # A05695-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SIX4 at approximately 95 kDa. The expected band size for SIX4 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05695-1-six4-primary-antibodies-if-testing-2.jpgAnti-SIX4 Antibody Picoband® IF analysis of SIX4 using anti-SIX4 antibody (A05695-1) and anti-Beta Tubulin antibody (M01857-3). SIX4 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SIX4 Antibody (A05695-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05695-1-six4-primary-antibodies-fcm-testing-3.pngAnti-SIX4 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-SIX4 antibody (A05695-1). Overlay histogram showing U20S cells stained with A05695-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SIX4 Antibody (A05695-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-sult1c4-picoband-trade-antibody-a10623-1-boster.html2026-03-17T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10623-1-sult1c4-primary-antibodies-wb-testing-1.jpgAnti-SULT1C4 Antibody Picoband® Western blot analysis of SULT1C4 using anti-SULT1C4 antibody (A10623-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SULT1C4 antigen affinity purified polyclonal antibody (Catalog # A10623-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SULT1C4 at approximately 38 kDa. The expected band size for SULT1C4 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10623-1-sult1c4-primary-antibodies-fcm-testing-2.pngAnti-SULT1C4 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-SULT1C4 antibody (A10623-1). Overlay histogram showing HepG2 cells stained with A10623-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SULT1C4 Antibody (A10623-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rufy3-picoband-trade-antibody-a09453-1-boster.html2026-03-17T05:14:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09453-1-rufy3-primary-antibodies-wb-testing-1.jpgAnti-RUFY3 Antibody Picoband® Western blot analysis of RUFY3 using anti-RUFY3 antibody (A09453-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RUFY3 antigen affinity purified polyclonal antibody (Catalog # A09453-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RUFY3 at approximately 53-65 kDa. The expected band size for RUFY3 is at 53-65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09453-1-rufy3-primary-antibodies-fcm-testing-2.pngAnti-RUFY3 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-RUFY3 antibody (A09453-1). Overlay histogram showing SH-SY5Y cells stained with A09453-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RUFY3 Antibody (A09453-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-papss2-picoband-trade-antibody-a05684-1-boster.html2026-03-17T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-wb-testing-1.jpgAnti-PAPSS2 Antibody Picoband® Western blot analysis of PAPSS2 using anti-PAPSS2 antibody (A05684-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: rat kidney tissue lysates, Lane 4: mouse liver tissue lysates, Lane 5: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAPSS2 antigen affinity purified polyclonal antibody (Catalog # A05684-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAPSS2 at approximately 70 kDa. The expected band size for PAPSS2 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-ihc-testing-2.jpgAnti-PAPSS2 Antibody Picoband® IHC analysis of PAPSS2 using anti-PAPSS2 antibody (A05684-1). PAPSS2 was detected in a paraffin-embedded section of human adrenocortical adenoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAPSS2 Antibody (A05684-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-ihc-testing-3.jpgAnti-PAPSS2 Antibody Picoband® IHC analysis of PAPSS2 using anti-PAPSS2 antibody (A05684-1). PAPSS2 was detected in a paraffin-embedded section of human laryngeal squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAPSS2 Antibody (A05684-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-ihc-testing-4.jpgAnti-PAPSS2 Antibody Picoband® IHC analysis of PAPSS2 using anti-PAPSS2 antibody (A05684-1). PAPSS2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAPSS2 Antibody (A05684-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-ihc-testing-5.jpgAnti-PAPSS2 Antibody Picoband® IHC analysis of PAPSS2 using anti-PAPSS2 antibody (A05684-1). PAPSS2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAPSS2 Antibody (A05684-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-if-testing-6.jpgAnti-PAPSS2 Antibody Picoband® IF analysis of PAPSS2 using anti-PAPSS2 antibody (A05684-1). PAPSS2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/mL rabbit anti-PAPSS2 Antibody (A05684-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-if-testing-7.jpgAnti-PAPSS2 Antibody Picoband® IF analysis of PAPSS2 using anti-PAPSS2 antibody (A05684-1). PAPSS2 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/mL rabbit anti-PAPSS2 Antibody (A05684-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05684-1-papss2-primary-antibodies-fcm-testing-8.pngAnti-PAPSS2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PAPSS2 antibody (A05684-1). Overlay histogram showing MCF-7 cells stained with A05684-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PAPSS2 Antibody (A05684-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-phf1-picoband-trade-antibody-a03758-2-boster.html2026-03-17T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03758-2-phf1-primary-antibodies-wb-testing-1.jpgAnti-PHF1 Antibody Picoband® Western blot analysis of PHF1 using anti-PHF1 antibody (A03758-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates, Lane 3: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF1 antigen affinity purified polyclonal antibody (Catalog # A03758-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHF1 at approximately 62 kDa. The expected band size for PHF1 is at 62 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-prmt6-picoband-trade-antibody-a02924-1-boster.html2026-03-17T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02924-1-prmt6-primary-antibodies-wb-testing-1.jpgAnti-PRMT6 Antibody Picoband® Western blot analysis of PRMT6 using anti-PRMT6 antibody (A02924-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRMT6 antigen affinity purified polyclonal antibody (Catalog # A02924-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRMT6 at approximately 40 kDa. The expected band size for PRMT6 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02924-1-prmt6-primary-antibodies-fcm-testing-2.pngAnti-PRMT6 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PRMT6 antibody (A02924-1). Overlay histogram showing SH-SY5Y cells stained with A02924-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PRMT6 Antibody (A02924-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-prmt7-picoband-trade-antibody-a05485-2-boster.html2026-03-17T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05485-2-prm7-primary-antibodies-wb-testing-1.jpgAnti-PRMT7 Antibody Picoband® Western blot analysis of PRMT7 using anti-PRMT7 antibody (A05485-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRMT7 antigen affinity purified polyclonal antibody (Catalog # A05485-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRMT7 at approximately 78 kDa. The expected band size for PRMT7 is at 78 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05485-2-prm7-primary-antibodies-ihc-testing-2.jpgAnti-PRMT7 Antibody Picoband® IHC analysis of PRMT7 using anti-PRMT7 antibody (A05485-2). PRMT7 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PRMT7 Antibody (A05485-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05485-2-prm7-primary-antibodies-ihc-testing-3.jpgAnti-PRMT7 Antibody Picoband® IHC analysis of PRMT7 using anti-PRMT7 antibody (A05485-2). PRMT7 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PRMT7 Antibody (A05485-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05485-2-prm7-primary-antibodies-ihc-testing-4.jpgAnti-PRMT7 Antibody Picoband® IHC analysis of PRMT7 using anti-PRMT7 antibody (A05485-2). PRMT7 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PRMT7 Antibody (A05485-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05485-2-prm7-primary-antibodies-if-testing-1.jpgAnti-PRMT7 Antibody Picoband®IF analysis of PRMT7 using anti-PRMT7 antibody (A05485-2) and anti-Tubulin Alpha antibody (M03989-3). PRMT7 was detected in immunocytochemical section of CACO-2 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PRMT7 Antibody (A05485-2) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05485-2-prm7-primary-antibodies-fcm-testing-5.pngAnti-PRMT7 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PRMT7 antibody (A05485-2). Overlay histogram showing HepG2 cells stained with A05485-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PRMT7 Antibody (A05485-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-abcc3-picoband-trade-antibody-a02429-2-boster.html2026-03-17T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02429-2-abcc3-primary-antibodies-wb-testing-1.jpgAnti-ABCC3 Antibody Picoband® Western blot analysis of ABCC3 using anti-ABCC3 antibody (A02429-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCC3 antigen affinity purified polyclonal antibody (Catalog # A02429-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ABCC3 at approximately 200 kDa. The expected band size for ABCC3 is at 200 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02429-2-abcc3-primary-antibodies-fcm-testing-2.pngAnti-ABCC3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ABCC3 antibody (A02429-2). Overlay histogram showing HepG2 cells stained with A02429-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ABCC3 Antibody (A02429-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-tsc22d1-picoband-trade-antibody-a06397-2-boster.html2026-03-17T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06397-2-tsc22d1-primary-antibodies-wb-testing-1.jpgAnti-TSC22D1 Antibody Picoband® Western blot analysis of TSC22D1 using anti-TSC22D1 antibody (A06397-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSC22D1 antigen affinity purified polyclonal antibody (Catalog # A06397-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TSC22D1 at approximately 140-150 kDa. The expected band size for TSC22D1 is at 140-150 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06397-2-tsc22d1-primary-antibodies-fcm-testing-2.pngAnti-TSC22D1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-TSC22D1 antibody (A06397-2). Overlay histogram showing SH-SY5Y cells stained with A06397-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TSC22D1 Antibody (A06397-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-naprt-picoband-trade-antibody-a10553-1-boster.html2026-03-17T05:15:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10553-1-naprt-primary-antibodies-wb-testing-1.jpgAnti-NAPRT Antibody Picoband® Western blot analysis of NAPRT using anti-NAPRT antibody (A10553-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAPRT antigen affinity purified polyclonal antibody (Catalog # A10553-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAPRT at approximately 58 kDa. The expected band size for NAPRT is at 58 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-narf-picoband-trade-antibody-a10513-2-boster.html2026-03-17T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10513-2-narf-primary-antibodies-wb-testing-1.jpgAnti-NARF Antibody Picoband® Western blot analysis of NARF using anti-NARF antibody (A10513-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NARF antigen affinity purified polyclonal antibody (Catalog # A10513-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NARF at approximately 52 kDa. The expected band size for NARF is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10513-2-narf-primary-antibodies-fcm-testing-2.pngAnti-NARF Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NARF antibody (A10513-2). Overlay histogram showing 293T cells stained with A10513-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NARF Antibody (A10513-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ttc39b-picoband-trade-antibody-a13852-1-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13852-1-ttc39b-primary-antibodies-wb-testing-1.jpgAnti-TTC39B Antibody Picoband® Western blot analysis of TTC39B using anti-TTC39B antibody (A13852-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TTC39B antigen affinity purified polyclonal antibody (Catalog # A13852-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TTC39B at approximately 70 kDa. The expected band size for TTC39B is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13852-1-ttc39b-primary-antibodies-fcm-testing-2.pngAnti-TTC39B Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-TTC39B antibody (A13852-1). Overlay histogram showing HepG2 cells stained with A13852-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TTC39B Antibody (A13852-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-selenon-picoband-trade-antibody-a31971-1-boster.html2026-03-17T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31971-1-selenon-primary-antibodies-wb-testing-1.jpgAnti-SELENON Antibody Picoband® Western blot analysis of SELENON using anti-SELENON antibody (A31971-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SELENON antigen affinity purified polyclonal antibody (Catalog # A31971-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SELENON at approximately 66-70 kDa. The expected band size for SELENON is at 66-70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31971-1-selenon-primary-antibodies-fcm-testing-2.pngAnti-SELENON Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-SELENON antibody (A31971-1). Overlay histogram showing HEL cells stained with A31971-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SELENON Antibody (A31971-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rufy1-picoband-trade-antibody-a10201-1-boster.html2026-03-17T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10201-1-rufy1-primary-antibodies-wb-testing-1.jpgAnti-RUFY1 Antibody Picoband® Western blot analysis of RUFY1 using anti-RUFY1 antibody (A10201-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RUFY1 antigen affinity purified polyclonal antibody (Catalog # A10201-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RUFY1 at approximately 80 kDa. The expected band size for RUFY1 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10201-1-rufy1-primary-antibodies-fcm-testing-2.pngAnti-RUFY1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-RUFY1 antibody (A10201-1). Overlay histogram showing MCF-7 cells stained with A10201-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RUFY1 Antibody (A10201-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-prodh-picoband-trade-antibody-a03231-3-boster.html2026-03-17T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03231-3-prodh-primary-antibodies-wb-testing-1.jpgAnti-PRODH Antibody Picoband® Western blot analysis of PRODH using anti-PRODH antibody (A03231-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates, Lane 3: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRODH antigen affinity purified polyclonal antibody (Catalog # A03231-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRODH at approximately 69 kDa. The expected band size for PRODH is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03231-3-prodh-primary-antibodies-ihc-testing-2.jpgAnti-PRODH Antibody Picoband® IHC analysis of PRODH using anti-PRODH antibody (A03231-3). PRODH was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PRODH Antibody (A03231-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03231-3-prodh-primary-antibodies-fcm-testing-3.pngAnti-PRODH Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PRODH antibody (A03231-3). Overlay histogram showing RT4 cells stained with A03231-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PRODH Antibody (A03231-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-proser3-picoband-trade-antibody-a16383-1-boster.html2026-03-17T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16383-1-proser3-primary-antibodies-wb-testing-1.jpgAnti-PROSER3 Antibody Picoband® Western blot analysis of PROSER3 using anti-PROSER3 antibody (A16383-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PROSER3 antigen affinity purified polyclonal antibody (Catalog # A16383-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PROSER3 at approximately 36 kDa. The expected band size for PROSER3 is at 53,36,20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16383-1-proser3-primary-antibodies-ihc-testing-2.jpgAnti-PROSER3 Antibody Picoband® IHC analysis of PROSER3 using anti-PROSER3 antibody (A16383-1). PROSER3 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PROSER3 Antibody (A16383-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-syndig4-prrt1-picoband-trade-antibody-a13564-1-boster.html2026-03-17T05:15:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13564-1-prrt-primary-antibodies-wb-testing-1.jpgAnti-SynDIG4/PRRT1 Antibody Picoband® Western blot analysis of SynDIG4/PRRT1 using anti-SynDIG4/PRRT1 antibody (A13564-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SynDIG4/PRRT1 antigen affinity purified polyclonal antibody (Catalog # A13564-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SynDIG4/PRRT1 at approximately 36 kDa. The expected band size for SynDIG4/PRRT1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13564-1-prrt-primary-antibodies-ihc-testing-2.jpgAnti-SynDIG4/PRRT1 Antibody Picoband® IHC analysis of SynDIG4/PRRT1 using anti-SynDIG4/PRRT1 antibody (A13564-1). SynDIG4/PRRT1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SynDIG4/PRRT1 Antibody (A13564-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13564-1-prrt-primary-antibodies-ihc-testing-3.jpgAnti-SynDIG4/PRRT1 Antibody Picoband® IHC analysis of SynDIG4/PRRT1 using anti-SynDIG4/PRRT1 antibody (A13564-1). SynDIG4/PRRT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SynDIG4/PRRT1 Antibody (A13564-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13564-1-prrt-primary-antibodies-if-testing-4.jpgAnti-SynDIG4/PRRT1 Antibody Picoband® IF analysis of SynDIG4/PRRT1 using anti-SynDIG4/PRRT1 antibody (A13564-1). SynDIG4/PRRT1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SynDIG4/PRRT1 Antibody (A13564-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13564-1-prrt-primary-antibodies-fcm-testing-5.pngAnti-SynDIG4/PRRT1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-SynDIG4/PRRT1 antibody (A13564-1). Overlay histogram showing SH-SY5Y cells stained with A13564-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SynDIG4/PRRT1 Antibody (A13564-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pspc1-picoband-trade-antibody-a06348-1-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06348-1-pspc1-primary-antibodies-wb-testing-1.jpgAnti-PSPC1 Antibody Picoband® Western blot analysis of PSPC1 using anti-PSPC1 antibody (A06348-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSPC1 antigen affinity purified polyclonal antibody (Catalog # A06348-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSPC1 at approximately 66 kDa. The expected band size for PSPC1 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06348-1-pspc1-primary-antibodies-ihc-testing-2.jpgAnti-PSPC1 Antibody Picoband® IHC analysis of PSPC1 using anti-PSPC1 antibody (A16132-1). PSPC1 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSPC1 Antibody (A16132-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06348-1-pspc1-primary-antibodies-ihc-testing-3.jpgAnti-PSPC1 Antibody Picoband® IHC analysis of PSPC1 using anti-PSPC1 antibody (A16132-1). PSPC1 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSPC1 Antibody (A16132-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06348-1-pspc1-primary-antibodies-if-testing-4.jpgAnti-PSPC1 Antibody Picoband® IF analysis of PSPC1 using anti-PSPC1 antibody (A06348-1) and anti-Beta Tubulin antibody (M01857-3). PSPC1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PSPC1 Antibody (A06348-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06348-1-pspc1-primary-antibodies-fcm-testing-5.pngAnti-PSPC1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-PSPC1 antibody (A06348-1). Overlay histogram showing HEL cells stained with A06348-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSPC1 Antibody (A06348-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pstpip2-picoband-trade-antibody-a11056-1-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11056-1-pstpip2-primary-antibodies-wb-testing-1.jpgAnti-PSTPIP2 Antibody Picoband® Western blot analysis of PSTPIP2 using anti-PSTPIP2 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSTPIP2 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSTPIP2 at approximately 36,39 kDa. The expected band size for PSTPIP2 is at 36,39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11056-1-pstpip2-primary-antibodies-if-testing-2.jpgAnti-PSTPIP2 Antibody Picoband® IF analysis of PSTPIP2 using anti-PSTPIP2 antibody (A11056-1). PSTPIP2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PSTPIP2 Antibody (A11056-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11056-1-pstpip2-primary-antibodies-fcm-testing-3.pngAnti-PSTPIP2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-PSTPIP2 antibody (A11056-1). Overlay histogram showing HEL cells stained with A11056-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSTPIP2 Antibody (A11056-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-chd8-picoband-trade-antibody-a01346-1-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01346-1-chd8-primary-antibodies-wb-testing-1.jpgAnti-CHD8 Antibody Picoband® Western blot analysis of CHD8 using anti-CHD8 antibody (A01346-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHD8 antigen affinity purified polyclonal antibody (Catalog # A01346-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHD8 at approximately 300 kDa. The expected band size for CHD8 is at 300 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01346-1-chd8-primary-antibodies-ihc-testing-2.jpgAnti-CHD8 Antibody Picoband® IHC analysis of CHD8 using anti-CHD8 antibody (A01346-1). CHD8 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHD8 Antibody (A01346-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01346-1-chd8-primary-antibodies-fcm-testing-3.pngAnti-CHD8 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-CHD8 antibody (A01346-1). Overlay histogram showing SH-SY5Y cells stained with A01346-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHD8 Antibody (A01346-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-gli2-picoband-trade-antibody-a00701-6-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00701-6-gli2-primary-antibodies-wb-testing-1.jpgAnti-GLI2 Antibody Picoband® Western blot analysis of GLI2 using anti-GLI2 antibody (A00701-6). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: rat brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLI2 antigen affinity purified polyclonal antibody (Catalog # A00701-6) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLI2 at approximately 180-200 kDa. The expected band size for GLI2 is at 220 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00701-6-gli2-primary-antibodies-ihc-testing-2.jpgAnti-GLI2 Antibody Picoband® IHC analysis of GLI2 using anti-GLI2 antibody (A00701-6). GLI2 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLI2 Antibody (A00701-6) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00701-6-gli2-primary-antibodies-ihc-testing-3.jpgAnti-GLI2 Antibody Picoband® IHC analysis of GLI2 using anti-GLI2 antibody (A00701-6). GLI2 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLI2 Antibody (A00701-6) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00701-6-gli2-primary-antibodies-ihc-testing-4.jpgAnti-GLI2 Antibody Picoband® IHC analysis of GLI2 using anti-GLI2 antibody (A00701-6). GLI2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLI2 Antibody (A00701-6) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00701-6-gli2-primary-antibodies-if-testing-5.jpgAnti-GLI2 Antibody Picoband® IF analysis of GLI2 using anti-GLI2 antibody (A00701-6) and anti-Beta Tubulin antibody (M01857-3). GLI2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GLI2 Antibody (A00701-6) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00701-6-gli2-primary-antibodies-fcm-testing-6.pngAnti-GLI2 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-GLI2 antibody (A00701-6). Overlay histogram showing U20S cells stained with A00701-6 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLI2 Antibody (A00701-6, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-klk7-picoband-trade-antibody-a02739-1-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02739-1-klk7-primary-antibodies-wb-testing-1.jpgAnti-Klk7 Antibody Picoband® Western blot analysis of Klk7 using anti-Klk7 antibody (A02739-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Klk7 antigen affinity purified polyclonal antibody (Catalog # A02739-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Klk7 at approximately 38 kDa. The expected band size for Klk7 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02739-1-klk7-primary-antibodies-ihc-testing-2.jpgAnti-Klk7 Antibody Picoband® IHC analysis of Klk7 using anti-Klk7 antibody (A02739-1). Klk7 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Klk7 Antibody (A02739-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-ncx1-slc8a1-picoband-trade-antibody-a03876-2-boster.html2026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03876-2-slc8a1-primary-antibodies-wb-testing-1.jpgAnti-NCX1/SLC8A1 Antibody Picoband® Western blot analysis of NCX1/SLC8A1 using anti-NCX1/SLC8A1 antibody (A03876-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NCX1/SLC8A1 antigen affinity purified polyclonal antibody (Catalog # A03876-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NCX1/SLC8A1 at approximately 120 kDa. The expected band size for NCX1/SLC8A1 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03876-2-slc8a1-primary-antibodies-if-testing-2.jpgAnti-NCX1/SLC8A1 Antibody Picoband® IF analysis of SLC8A1 using anti-SLC8A1 antibody (A03876-2). SLC8A1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SLC8A1 Antibody (A03876-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 594 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-pus7-picoband-trade-antibody-a13434-1-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13434-1-pus7-primary-antibodies-wb-testing-1_1.jpgAnti-PUS7 Antibody Picoband®Western blot analysis of PUS7 using anti-PUS7 antibody (A13434-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PUS7 antigen affinity purified polyclonal antibody (A13434-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PUS7 at approximately 75 kDa. The expected band size for PUS7 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13434-1-pus7-primary-antibodies-ihc-testing-1.jpgAnti-PUS7 Antibody Picoband®IHC analysis of PUS7 using anti-PUS7 antibody (A13434-1). PUS7 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PUS7 Antibody (A13434-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13434-1-pus7-primary-antibodies-ihc-testing-2.jpgAnti-PUS7 Antibody Picoband®IHC analysis of PUS7 using anti-PUS7 antibody (A13434-1). PUS7 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PUS7 Antibody (A13434-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13434-1-pus7-primary-antibodies-ihc-testing-3.jpgAnti-PUS7 Antibody Picoband®IHC analysis of PUS7 using anti-PUS7 antibody (A13434-1). PUS7 was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PUS7 Antibody (A13434-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13434-1-pus7-primary-antibodies-if-testing-1.jpgAnti-PUS7 Antibody Picoband®IF analysis of PUS7 using anti-PUS7 antibody (A13434-1) and anti-Tubulin Alpha antibody (M03989-3). PUS7 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PUS7 Antibody (A13434-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13434-1-pus7-primary-antibodies-if-testing-2.jpgAnti-PUS7 Antibody Picoband®IF analysis of PUS7 using anti-PUS7 antibody (A13434-1). PUS7 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PUS7 Antibody (A13434-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1031) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13434-1-pus7-primary-antibodies-fcm-testing-1.jpgAnti-PUS7 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-PUS7 antibody (A13434-1). Overlay histogram showing MCF-7 cells stained with A13434-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PUS7 Antibody (A13434-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-pus7l-picoband-trade-antibody-a14523-1-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14523-1-pus7l-primary-antibodies-wb-testing-1_1.jpgAnti-PUS7L Antibody Picoband®Western blot analysis of PUS7L using anti-PUS7L antibody (A14523-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human CACO-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PUS7L antigen affinity purified polyclonal antibody (Catalog # A14523-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PUS7L at approximately 81 kDa. The expected band size for PUS7L is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14523-1-pus7l-primary-antibodies-ihc-testing-1.jpgAnti-PUS7L Antibody Picoband®IHC analysis of PUS7L using anti-PUS7L antibody (A14523-1). PUS7L was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PUS7L Antibody (A14523-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14523-1-pus7l-primary-antibodies-ihc-testing-2.jpgAnti-PUS7L Antibody Picoband®IHC analysis of PUS7L using anti-PUS7L antibody (A14523-1). PUS7L was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PUS7L Antibody (A14523-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14523-1-pus7l-primary-antibodies-if-testing-1.jpgAnti-PUS7L Antibody Picoband®IF analysis of PUS7L using anti-PUS7L antibody (A14523-1). PUS7L was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PUS7L Antibody (A14523-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14523-1-pus7l-primary-antibodies-if-testing-2.jpgAnti-PUS7L Antibody Picoband®IF analysis of PUS7L using anti-PUS7L antibody (A14523-1). PUS7L was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PUS7L Antibody (A14523-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14523-1-pus7l-primary-antibodies-ip-testing-1.jpgAnti-PUS7L Antibody Picoband®Immunoprecipitating (IP) PUS7L in Hela whole cell lysate. Western blot analysis of PUS7L using anti-PUS7L antibody (A14523-1); Lane 1: Hela whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-PUS7L antibody in Hela whole cell lysate; Lane 3: anti-PUS7L antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PUS7L antigen affinity purified polyclonal antibody (A14523-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PUS7L at approximately 81 kDa. The expected band size for PUS7L is at 81 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nat10-picoband-trade-antibody-a06226-2-boster.html2026-03-17T05:15:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06226-2-nat10-primary-antibodies-wb-testing-1.jpgAnti-NAT10 Antibody Picoband® Western blot analysis of NAT10 using anti-NAT10 antibody (A06226-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAT10 antigen affinity purified polyclonal antibody (Catalog # A06226-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAT10 at approximately 120 kDa. The expected band size for NAT10 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06226-2-nat10-primary-antibodies-if-testing-2.jpgAnti-NAT10 Antibody Picoband® IF analysis of NAT10 using anti-NAT10 antibody (A06226-2) and anti-Beta Tubulin antibody (M01857-3). NAT10 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NAT10 Antibody (A06226-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06226-2-nat10-primary-antibodies-if-testing-3.jpgAnti-NAT10 Antibody Picoband® IF analysis of NAT10 using anti-NAT10 antibody (A06226-2) and anti-Tubulin Alpha antibody (M03989-3). NAT10 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NAT10 Antibody (A06226-2) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06226-2-nat10-primary-antibodies-ip-testing-1.jpgAnti-NAT10 Antibody Picoband®Immunoprecipitating (IP) NAT10 in 293T whole cell lysate. Western blot analysis of NAT10 using anti-NAT10 antibody (A06226-2); Lane 1: 293T whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-NAT10 antibody in 293T whole cell lysate; Lane 3: anti-NAT10 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NAT10 antigen affinity purified polyclonal antibody (A06226-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NAT10 at approximately 120 kDa. The expected band size for NAT10 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06226-2-nat10-primary-antibodies-fcm-testing-4.jpgAnti-NAT10 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-NAT10 antibody (A06226-2). Overlay histogram showing Hela cells stained with A06226-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAT10 Antibody (A06226-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-tgm2-picoband-trade-antibody-a02229-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02229-tgm2-primary-antibodies-wb-testing-1.jpgAnti-TGM2 Antibody Picoband® Western blot analysis of TGM2 using anti-TGM2 antibody (A02229). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human placenta tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TGM2 antigen affinity purified polyclonal antibody (Catalog # A02229) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TGM2 at approximately 80 kDa. The expected band size for TGM2 is at 80 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-ghrh-picoband-trade-antibody-a01699-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01699-1-ghrh-primary-antibodies-wb-testing-1.jpgAnti-GHRH Antibody Picoband® Western blot analysis of GHRH using anti-GHRH antibody (A01699-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat lung tissue lysates, Lane 2: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GHRH antigen affinity purified polyclonal antibody (Catalog # A01699-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GHRH at approximately 13-15 kDa. The expected band size for GHRH is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01699-1-ghrh-primary-antibodies-ihc-testing-2.jpgAnti-GHRH Antibody Picoband® IHC analysis of GHRH using anti-GHRH antibody (A01699-1). GHRH was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GHRH Antibody (A01699-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01699-1-ghrh-primary-antibodies-ihc-testing-3_1.jpgAnti-GHRH Antibody Picoband® IHC analysis of GHRH using anti-GHRH antibody (A01699-1). GHRH was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GHRH Antibody (A01699-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-sox10-picoband-trade-antibody-a00758-3-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-3-sox10-primary-antibodies-wb-testing-1.jpgAnti-SOX10 Antibody Picoband® Western blot analysis of SOX10 using anti-SOX10 antibody (A00758-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOX10 antigen affinity purified polyclonal antibody (Catalog # A00758-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX10 at approximately 60-65 kDa. The expected band size for SOX10 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-3-sox10-primary-antibodies-if-testing-2.jpgAnti-SOX10 Antibody Picoband® IF analysis of SOX10 using anti-SOX10 antibody (A00758-3). SOX10 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SOX10 Antibody (A00758-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-3-sox10-primary-antibodies-if-testing-1.jpgAnti-SOX10 Antibody Picoband®IF analysis of SOX10 using anti-SOX10 antibody (A00758-3). SOX10 was detected in an immunocytochemical section of human A-375 cells. The cells were fixed with 4% paraformaldehyde for 10 minutes and then treated with a membrane permeabilization agent (AR0205) for 5 minutes.The cells were blocked with 10% goat serum. And then incubated with rabbit anti-SOX10 Antibody (A00758-3) at a dilution of 10 ug/mL overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00758-3-sox10-primary-antibodies-fcm-testing-3.pngAnti-SOX10 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-SOX10 antibody (A00758-3). Overlay histogram showing PC-3 cells stained with A00758-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SOX10 Antibody (A00758-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-acat1-picoband-trade-antibody-a02008-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02008-1-acat1-primary-antibodies-wb-testing-1.jpgAnti-ACAT1 Antibody Picoband® Western blot analysis of ACAT1 using anti-ACAT1 antibody (A02008-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat skeletal muscle tissue lysates, Lane 7: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACAT1 antigen affinity purified polyclonal antibody (Catalog # A02008-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACAT1 at approximately 40 kDa. The expected band size for ACAT1 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02008-1-acat1-primary-antibodies-ihc-testing-2.jpgAnti-ACAT1 Antibody Picoband® IHC analysis of ACAT1 using anti-ACAT1 antibody (A02008-1). ACAT1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACAT1 Antibody (A02008-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02008-1-acat1-primary-antibodies-ihc-testing-3.jpgAnti-ACAT1 Antibody Picoband® IHC analysis of ACAT1 using anti-ACAT1 antibody (A02008-1). ACAT1 was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACAT1 Antibody (A02008-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02008-1-acat1-primary-antibodies-ihc-testing-4.jpgAnti-ACAT1 Antibody Picoband® IHC analysis of ACAT1 using anti-ACAT1 antibody (A02008-1). ACAT1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACAT1 Antibody (A02008-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02008-1-acat1-primary-antibodies-if-testing-5.jpgAnti-ACAT1 Antibody Picoband® IF analysis of ACAT1 using anti-ACAT1 antibody (A02008-1). ACAT1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ACAT1 Antibody (A02008-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02008-1-acat1-primary-antibodies-fcm-testing-6.pngAnti-ACAT1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-ACAT1 antibody (A02008-1). Overlay histogram showing MCF-7 cells stained with A02008-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ACAT1 Antibody (A02008-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pter-picoband-trade-antibody-a08763-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08763-1-pter-primary-antibodies-wb-testing-1.jpgAnti-PTER Antibody Picoband® Western blot analysis of PTER using anti-PTER antibody (A08763-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTER antigen affinity purified polyclonal antibody (Catalog # A08763-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTER at approximately 39 kDa. The expected band size for PTER is at 39 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-pth2r-picoband-trade-antibody-a10343-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10343-1-pth2r-primary-antibodies-wb-testing-1.jpgAnti-PTH2R Antibody Picoband® Western blot analysis of PTH2R using anti-PTH2R antibody (A10343-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTH2R antigen affinity purified polyclonal antibody (Catalog # A10343-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTH2R at approximately 75 kDa. The expected band size for PTH2R is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10343-1-pth2r-primary-antibodies-if-testing-2.jpgAnti-PTH2R Antibody Picoband® IF analysis of PTH2R using anti-PTH2R antibody (A10343-1). PTH2R was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PTH2R Antibody (A10343-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-ptpn13-picoband-trade-antibody-a02481-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02481-1-ptpn13-primary-antibodies-wb-testing-1.jpgAnti-PTPN13 Antibody Picoband® Western blot analysis of PTPN13 using anti-PTPN13 antibody (A02481-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTPN13 antigen affinity purified polyclonal antibody (Catalog # A02481-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTPN13 at approximately 270 kDa. The expected band size for PTPN13 is at 270 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02481-1-ptpn13-primary-antibodies-fcm-testing-2.pngAnti-PTPN13 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PTPN13 antibody (A02481-1). Overlay histogram showing RT4 cells stained with A02481-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PTPN13 Antibody (A02481-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ncoa5-picoband-trade-antibody-a07810-2-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-wb-testing-1.jpgAnti-NCOA5 Antibody Picoband® Western blot analysis of NCOA5 using anti-NCOA5 antibody (A07810-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NCOA5 antigen affinity purified polyclonal antibody (Catalog # A07810-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NCOA5 at approximately 66 kDa. The expected band size for NCOA5 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-ihc-testing-2.jpgAnti-NCOA5 Antibody Picoband® IHC analysis of NCOA5 using anti-NCOA5 antibody (A07810-2). NCOA5 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCOA5 Antibody (A07810-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-ihc-testing-3.jpgAnti-NCOA5 Antibody Picoband® IHC analysis of NCOA5 using anti-NCOA5 antibody (A07810-2). NCOA5 was detected in a paraffin-embedded section of human colorectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCOA5 Antibody (A07810-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-ihc-testing-4.jpgAnti-NCOA5 Antibody Picoband® IHC analysis of NCOA5 using anti-NCOA5 antibody (A07810-2). NCOA5 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCOA5 Antibody (A07810-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-ihc-testing-5.jpgAnti-NCOA5 Antibody Picoband® IHC analysis of NCOA5 using anti-NCOA5 antibody (A07810-2). NCOA5 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCOA5 Antibody (A07810-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-ihc-testing-6.jpgAnti-NCOA5 Antibody Picoband® IHC analysis of NCOA5 using anti-NCOA5 antibody (A07810-2). NCOA5 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCOA5 Antibody (A07810-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-if-testing-7.jpgAnti-NCOA5 Antibody Picoband® IF analysis of NCOA5 using anti-NCOA5 antibody (A07810-2) and anti-Beta Tubulin antibody (M01857-3). NCOA5 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NCOA5 Antibody (A07810-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07810-2-ncoa5-primary-antibodies-fcm-testing-8.jpgAnti-NCOA5 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NCOA5 antibody (A07810-2). Overlay histogram showing 293T cells stained with A07810-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NCOA5 Antibody (A07810-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-nit2-picoband-trade-antibody-a05891-3-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05891-3-nit2-primary-antibodies-wb-testing-1.jpgAnti-NIT2 Antibody Picoband® Western blot analysis of NIT2 using anti-NIT2 antibody (A05891-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: rat kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NIT2 antigen affinity purified polyclonal antibody (Catalog # A05891-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NIT2 at approximately 33 kDa. The expected band size for NIT2 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05891-3-nit2-primary-antibodies-ihc-testing-2.jpgAnti-NIT2 Antibody Picoband® IHC analysis of NIT2 using anti-NIT2 antibody (A05891-3). NIT2 was detected in a paraffin-embedded section of human squamous cell carcinoma penis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NIT2 Antibody (A05891-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05891-3-nit2-primary-antibodies-ihc-testing-3.jpgAnti-NIT2 Antibody Picoband® IHC analysis of NIT2 using anti-NIT2 antibody (A05891-3). NIT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NIT2 Antibody (A05891-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05891-3-nit2-primary-antibodies-ihc-testing-4.jpgAnti-NIT2 Antibody Picoband® IHC analysis of NIT2 using anti-NIT2 antibody (A05891-3). NIT2 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NIT2 Antibody (A05891-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05891-3-nit2-primary-antibodies-ihc-testing-5.jpgAnti-NIT2 Antibody Picoband® IHC analysis of NIT2 using anti-NIT2 antibody (A05891-3). NIT2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NIT2 Antibody (A05891-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05891-3-nit2-primary-antibodies-fcm-testing-6.pngAnti-NIT2 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-NIT2 antibody (A05891-3). Overlay histogram showing A549 cells stained with A05891-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NIT2 Antibody (A05891-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nme6-picoband-trade-antibody-a10922-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10922-1-nme6-primary-antibodies-wb-testing-1.jpgAnti-NME6 Antibody Picoband® Western blot analysis of NME6 using anti-NME6 antibody (A10922-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Lncap whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NME6 antigen affinity purified polyclonal antibody (Catalog # A10922-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NME6 at approximately 21 kDa. The expected band size for NME6 is at 21 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-noc4l-picoband-trade-antibody-a15803-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15803-1-noc4l-primary-antibodies-wb-testing-1.jpgAnti-NOC4L Antibody Picoband® Western blot analysis of NOC4L using anti-NOC4L antibody (A15803-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOC4L antigen affinity purified polyclonal antibody (Catalog # A15803-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOC4L at approximately 58 kDa. The expected band size for NOC4L is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15803-1-noc4l-primary-antibodies-if-testing-2.jpgAnti-NOC4L Antibody Picoband® IF analysis of NOC4L using anti-NOC4L antibody (A15803-1) and anti-Beta Tubulin antibody (M01857-3). NOC4L was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NOC4L Antibody (A15803-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15803-1-noc4l-primary-antibodies-fcm-testing-3.pngAnti-NOC4L Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NOC4L antibody (A15803-1). Overlay histogram showing 293T cells stained with A15803-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NOC4L Antibody (A15803-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-npepps-picoband-trade-antibody-a08129-2-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08129-2-npepps-primary-antibodies-wb-testing-1.jpgAnti-NPEPPS Antibody Picoband® Western blot analysis of NPEPPS using anti-NPEPPS antibody (A08129-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse barin tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NPEPPS antigen affinity purified polyclonal antibody (Catalog # A08129-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NPEPPS at approximately 110 kDa. The expected band size for NPEPPS is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08129-2-npepps-primary-antibodies-ihc-testing-2.jpgAnti-NPEPPS Antibody Picoband® IHC analysis of NPEPPS using anti-NPEPPS antibody (A08129-2). NPEPPS was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPEPPS Antibody (A08129-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08129-2-npepps-primary-antibodies-ihc-testing-3.jpgAnti-NPEPPS Antibody Picoband® IHC analysis of NPEPPS using anti-NPEPPS antibody (A08129-2). NPEPPS was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPEPPS Antibody (A08129-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08129-2-npepps-primary-antibodies-ihc-testing-4.jpgAnti-NPEPPS Antibody Picoband® IHC analysis of NPEPPS using anti-NPEPPS antibody (A08129-2). NPEPPS was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPEPPS Antibody (A08129-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08129-2-npepps-primary-antibodies-fcm-testing-5.pngAnti-NPEPPS Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NPEPPS antibody (A08129-2). Overlay histogram showing 293T cells stained with A08129-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NPEPPS Antibody (A08129-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-npffr2-picoband-trade-antibody-a08389-2-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08389-2-npffr2-primary-antibodies-wb-testing-1.jpgAnti-NPFFR2 Antibody Picoband® Western blot analysis of NPFFR2 using anti-NPFFR2 antibody (A08389-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NPFFR2 antigen affinity purified polyclonal antibody (Catalog # A08389-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NPFFR2 at approximately 60 kDa. The expected band size for NPFFR2 is at 60 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nqo2-picoband-trade-antibody-a03112-1-boster.html2026-03-17T05:15:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03112-1-nqo2-primary-antibodies-wb-testing-1.jpgAnti-NQO2 Antibody Picoband® Western blot analysis of NQO2 using anti-NQO2 antibody (A03112-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NQO2 antigen affinity purified polyclonal antibody (Catalog # A03112-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NQO2 at approximately 26 kDa. The expected band size for NQO2 is at 26 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-tssk4-picoband-trade-antibody-a10441-3-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10441-3-tssk4-primary-antibodies-wb-testing-1.jpgAnti-TSSK4 Antibody Picoband® Western blot analysis of TSSK4 using anti-TSSK4 antibody (A10441-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TSSK4 antigen affinity purified polyclonal antibody (Catalog # A10441-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TSSK4 at approximately 42 kDa. The expected band size for TSSK4 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10441-3-tssk4-primary-antibodies-fcm-testing-2.pngAnti-TSSK4 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-TSSK4 antibody (A10441-3). Overlay histogram showing SH-SY5Y cells stained with A10441-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TSSK4 Antibody (A10441-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ptgr1-picoband-trade-antibody-a08587-1-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08587-1-ptgr1-primary-antibodies-wb-testing-1.jpgAnti-PTGR1 Antibody Picoband® Western blot analysis of PTGR1 using anti-PTGR1 antibody (A08587-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: human SiHa whole cell lysates, Lane 6: human Hacat whole cell lysates, Lane 7: human Caco-2 whole cell lysates, Lane 8: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTGR1 antigen affinity purified polyclonal antibody (Catalog # A08587-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTGR1 at approximately 36 kDa. The expected band size for PTGR1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08587-1-ptgr1-primary-antibodies-fcm-testing-2.pngAnti-PTGR1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PTGR1 antibody (A08587-1). Overlay histogram showing RT4 cells stained with A08587-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PTGR1 Antibody (A08587-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ptgr2-picoband-trade-antibody-a10106-2-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10106-2-ptgr2-primary-antibodies-wb-testing-1.jpgAnti-PTGR2 Antibody Picoband® Western blot analysis of PTGR2 using anti-PTGR2 antibody (A10106-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTGR2 antigen affinity purified polyclonal antibody (Catalog # A10106-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTGR2 at approximately 40 kDa. The expected band size for PTGR2 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10106-2-ptgr2-primary-antibodies-fcm-testing-2.pngAnti-PTGR2 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PTGR2 antibody (A10106-2). Overlay histogram showing RT4 cells stained with A10106-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PTGR2 Antibody (A10106-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ptpn9-picoband-trade-antibody-a08233-1-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08233-1-ptpn9-primary-antibodies-wb-testing-1.jpgAnti-PTPN9 Antibody Picoband® Western blot analysis of PTPN9 using anti-PTPN9 antibody (A08233-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTPN9 antigen affinity purified polyclonal antibody (Catalog # A08233-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTPN9 at approximately 70 kDa. The expected band size for PTPN9 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08233-1-ptpn9-primary-antibodies-fcm-testing-2.pngAnti-PTPN9 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PTPN9 antibody (A08233-1). Overlay histogram showing RT4 cells stained with A08233-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PTPN9 Antibody (A08233-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ovgp1-picoband-trade-antibody-a07911-1-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07911-1-ovgp1-primary-antibodies-wb-testing-1.jpgAnti-OVGP1 Antibody Picoband® Western blot analysis of OVGP1 using anti-OVGP1 antibody (A07911-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse ovary tissue lysates, Lane 7: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OVGP1 antigen affinity purified polyclonal antibody (Catalog # A07911-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OVGP1 at approximately 75 kDa. The expected band size for OVGP1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07911-1-ovgp1-primary-antibodies-fcm-testing-2.pngAnti-OVGP1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-OVGP1 antibody (A07911-1). Overlay histogram showing RT4 cells stained with A07911-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-OVGP1 Antibody (A07911-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nptxr-picoband-trade-antibody-a15505-1-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15505-1-nptxr-primary-antibodies-wb-testing-1_1.jpgAnti-NPTXR Antibody Picoband® Western blot analysis of NPTXR using anti-NPTXR antibody (A15505-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U87 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NPTXR antigen affinity purified polyclonal antibody (Catalog # A15505-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NPTXR at approximately 66 kDa. The expected band size for NPTXR is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15505-1-nptxr-primary-antibodies-ihc-testing-2_1.jpgAnti-NPTXR Antibody Picoband® IHC analysis of NPTXR using anti-NPTXR antibody (A15505-1). NPTXR was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPTXR Antibody (A15505-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15505-1-nptxr-primary-antibodies-ihc-testing-3_1.jpgAnti-NPTXR Antibody Picoband® IHC analysis of NPTXR using anti-NPTXR antibody (A15505-1). NPTXR was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPTXR Antibody (A15505-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15505-1-nptxr-primary-antibodies-ihc-testing-4_1.jpgAnti-NPTXR Antibody Picoband® IHC analysis of NPTXR using anti-NPTXR antibody (A15505-1). NPTXR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPTXR Antibody (A15505-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15505-1-nptxr-primary-antibodies-fcm-testing-5_1.jpgAnti-NPTXR Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-NPTXR antibody (A15505-1). Overlay histogram showing HepG2 cells stained with A15505-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NPTXR Antibody (A15505-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-dax-1-nr0b1-picoband-trade-antibody-a01521-2-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01521-2-nr0b1-primary-antibodies-wb-testing-1.jpgAnti-DAX-1/NR0B1 Antibody Picoband® Western blot analysis of DAX-1/NR0B1 using anti-DAX-1/NR0B1 antibody (A01521-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human U87 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DAX-1/NR0B1 antigen affinity purified polyclonal antibody (Catalog # A01521-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DAX-1/NR0B1 at approximately 48 kDa. The expected band size for DAX-1/NR0B1 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01521-2-nr0b1-primary-antibodies-if-testing-2.jpgAnti-DAX-1/NR0B1 Antibody Picoband® IF analysis of DAX-1/NR0B1 using anti-DAX-1/NR0B1 antibody (A01521-2) and anti-Beta Tubulin antibody (M01857-3). DAX-1/NR0B1 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DAX-1/NR0B1 Antibody (A01521-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-nvl-picoband-trade-antibody-a05446-3-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-wb-testing-1.jpgAnti-NVL Antibody Picoband® Western blot analysis of NVL using anti-NVL antibody (A05446-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NVL antigen affinity purified polyclonal antibody (Catalog # A05446-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NVL at approximately 95 kDa. The expected band size for NVL is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-2.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-3.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-4.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-5.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-6.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of human urothelial carcinoma with squamous differentiation tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-7.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of human lung adenocarcinoma with squamous differentiation tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-8.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-ihc-testing-9.jpgAnti-NVL Antibody Picoband® IHC analysis of NVL using anti-NVL antibody (A05446-3). NVL was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NVL Antibody (A05446-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-if-testing-10.jpgAnti-NVL Antibody Picoband® IF analysis of NVL using anti-NVL antibody (A05446-3) and anti-Beta Tubulin antibody (M01857-3). NVL was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NVL Antibody (A05446-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05446-3-nvl-primary-antibodies-fcm-testing-11.pngAnti-NVL Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NVL antibody (A05446-3). Overlay histogram showing 293T cells stained with A05446-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NVL Antibody (A05446-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nop2-picoband-trade-antibody-a04830-1-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04830-1-nop2-primary-antibodies-wb-testing-1.jpgAnti-NOP2 Antibody Picoband® Western blot analysis of NOP2 using anti-NOP2 antibody (A04830-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: human RT4 whole cell lysates, Lane 6: human 293T tissue lysates, Lane 7: human SIHA whole cell lyates, Lane 8: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOP2 antigen affinity purified polyclonal antibody (Catalog # A04830-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOP2 at approximately 120 kDa. The expected band size for NOP2 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04830-1-nop2-primary-antibodies-if-testing-2.jpgAnti-NOP2 Antibody Picoband® IF analysis of NOP2 using anti-NOP2 antibody (A04830-1) and anti-Beta Tubulin antibody (M01857-3). NOP2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NOP2 Antibody (A04830-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04830-1-nop2-primary-antibodies-fcm-testing-3.pngAnti-NOP2 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-NOP2 antibody (A04830-1). Overlay histogram showing RT4 cells stained with A04830-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NOP2 Antibody (A04830-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nosip-picoband-trade-antibody-a07558-2-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07558-2-nosip-primary-antibodies-wb-testing-1_1.jpgAnti-NOSIP Antibody Picoband® Western blot analysis of NOSIP using anti-NOSIP antibody (A07558-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOSIP antigen affinity purified polyclonal antibody (Catalog # A07558-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOSIP at approximately 35 kDa. The expected band size for NOSIP is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07558-2-nosip-primary-antibodies-if-testing-2_1.jpgAnti-NOSIP Antibody Picoband® IF analysis of NOSIP using anti-NOSIP antibody (A07558-2). NOSIP was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NOSIP Antibody (A07558-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 594 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07558-2-nosip-primary-antibodies-if-testing-3.jpgAnti-NOSIP Antibody Picoband® IF analysis of NOSIP using anti-NOSIP antibody (A07558-2) and Anti-Beta Tubulin Antibody (M01857-3). NOSIP was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NOSIP Antibody (A07558-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07558-2-nosip-primary-antibodies-fcm-testing-4.jpgAnti-NOSIP Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NOSIP antibody (A07558-2). Overlay histogram showing 293T cells stained with A07558-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NOSIP Antibody (A07558-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-nudc-picoband-trade-antibody-a00995-1-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00995-1-nudc-primary-antibodies-wb-testing-1.jpgAnti-NUDC Antibody Picoband® Western blot analysis of NUDC using anti-NUDC antibody (A00995-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDC antigen affinity purified polyclonal antibody (Catalog # A00995-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDC at approximately 43 kDa. The expected band size for NUDC is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00995-1-nudc-primary-antibodies-if-testing-2.jpgAnti-NUDC Antibody Picoband® IF analysis of NUDC using anti-NUDC antibody (A00995-1). NUDC was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUDC Antibody (A00995-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00995-1-nudc-primary-antibodies-fcm-testing-3.pngAnti-NUDC Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NUDC antibody (A00995-1). Overlay histogram showing 293T cells stained with A00995-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDC Antibody (A00995-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mdmx-mdm4-picoband-trade-antibody-a01889-2-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01889-2-mdm4-primary-antibodies-wb-testing-1.jpgAnti-MDMX/MDM4 Antibody Picoband® Western blot analysis of MDMX/MDM4 using anti-MDMX/MDM4 antibody (A01889-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MDMX/MDM4 antigen affinity purified polyclonal antibody (Catalog # A01889-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MDMX/MDM4 at approximately 55 kDa. The expected band size for MDMX/MDM4 is at 55 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-med12-picoband-trade-antibody-a00828-2-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00828-2-med12-primary-antibodies-wb-testing-1.jpgAnti-MED12 Antibody Picoband® Western blot analysis of MED12 using anti-MED12 antibody (A00828-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED12 antigen affinity purified polyclonal antibody (Catalog # A00828-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED12 at approximately 260 kDa. The expected band size for MED12 is at 260 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nudcd3-picoband-trade-antibody-a13207-1-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13207-1-nudcd3-primary-antibodies-wb-testing-1.jpgAnti-NUDCD3 Antibody Picoband® Western blot analysis of NUDCD3 using anti-NUDCD3 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDCD3 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDCD3 at approximately 45 kDa. The expected band size for NUDCD3 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13207-1-nudcd3-primary-antibodies-ihc-testing-2.jpgAnti-NUDCD3 Antibody Picoband® IHC analysis of NUDCD3 using anti-NUDCD3 antibody (A13207-1). NUDCD3 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDCD3 Antibody (A13207-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13207-1-nudcd3-primary-antibodies-ihc-testing-3.jpgAnti-NUDCD3 Antibody Picoband® IHC analysis of NUDCD3 using anti-NUDCD3 antibody (A13207-1). NUDCD3 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDCD3 Antibody (A13207-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13207-1-nudcd3-primary-antibodies-if-testing-4.jpgAnti-NUDCD3 Antibody Picoband® IF analysis of NUDCD3 using anti-NUDCD3 antibody (A13207-1). NUDCD3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUDCD3 Antibody (A13207-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13207-1-nudcd3-primary-antibodies-fcm-testing-5.pngAnti-NUDCD3 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-NUDCD3 antibody (A13207-1). Overlay histogram showing RT4 cells stained with A13207-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDCD3 Antibody (A13207-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nuf2-picoband-trade-antibody-a03788-2-boster.html2026-03-17T05:15:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03788-2-nuf2-primary-antibodies-wb-testing-1.jpgAnti-NUF2 Antibody Picoband® Western blot analysis of NUF2 using anti-NUF2 antibody (A03788-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUF2 antigen affinity purified polyclonal antibody (Catalog # A03788-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUF2 at approximately 54 kDa. The expected band size for NUF2 is at 54 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nufip1-picoband-trade-antibody-a10137-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10137-1-nufip1-primary-antibodies-wb-testing-1.jpgAnti-NUFIP1 Antibody Picoband® Western blot analysis of NUFIP1 using anti-NUFIP1 antibody (A10137-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A375 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: human 293T whole cell lysates, Lane 6: human HepG2 whole cell lysates, Lane 7: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUFIP1 antigen affinity purified polyclonal antibody (Catalog # A10137-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUFIP1 at approximately 75 kDa. The expected band size for NUFIP1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10137-1-nufip1-primary-antibodies-if-testing-2.jpgAnti-NUFIP1 Antibody Picoband® IF analysis of NUFIP1 using anti-NUFIP1 antibody (A10137-1) and anti-Beta Tubulin antibody (M01857-3). NUFIP1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUFIP1 Antibody (A10137-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-numa-numa1-picoband-trade-antibody-a02018-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02018-1-numa1-primary-antibodies-wb-testing-1.jpgAnti-NUMA/NUMA1 Antibody Picoband® Western blot analysis of NUMA/NUMA1 using anti-NUMA/NUMA1 antibody (A02018-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: monkey COS-7 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: human SIHA whole cell lysates, Lane 6: human RT4 whole cell lysates, Lane 7: rat PC-12 whole cell lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUMA/NUMA1 antigen affinity purified polyclonal antibody (Catalog # A02018-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUMA/NUMA1 at approximately 270 kDa. The expected band size for NUMA/NUMA1 is at 270 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02018-1-numa1-primary-antibodies-ihc-testing-2.jpgAnti-NUMA/NUMA1 Antibody Picoband® IHC analysis of NUMA/NUMA1 using anti-NUMA/NUMA1 antibody (A02018-1). NUMA/NUMA1 was detected in a paraffin-embedded section of human acinar adenocarcinoma of prostate tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUMA/NUMA1 Antibody (A02018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02018-1-numa1-primary-antibodies-ihc-testing-3.jpgAnti-NUMA/NUMA1 Antibody Picoband® IHC analysis of NUMA/NUMA1 using anti-NUMA/NUMA1 antibody (A02018-1). NUMA/NUMA1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUMA/NUMA1 Antibody (A02018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02018-1-numa1-primary-antibodies-ihc-testing-4.jpgAnti-NUMA/NUMA1 Antibody Picoband® IHC analysis of NUMA/NUMA1 using anti-NUMA/NUMA1 antibody (A02018-1). NUMA/NUMA1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUMA/NUMA1 Antibody (A02018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02018-1-numa1-primary-antibodies-ihc-testing-5.jpgAnti-NUMA/NUMA1 Antibody Picoband® IHC analysis of NUMA/NUMA1 using anti-NUMA/NUMA1 antibody (A02018-1). NUMA/NUMA1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUMA/NUMA1 Antibody (A02018-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02018-1-numa1-primary-antibodies-if-testing-6.jpgAnti-NUMA/NUMA1 Antibody Picoband® IF analysis of NUMA/NUMA1 using anti-NUMA/NUMA1 antibody (A02018-1) and anti-Beta Tubulin antibody (M01857-3). NUMA/NUMA1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUMA/NUMA1 Antibody (A02018-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02018-1-numa1-primary-antibodies-fcm-testing-7.pngAnti-NUMA/NUMA1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-NUMA/NUMA1 antibody (A02018-1). Overlay histogram showing RT4 cells stained with A02018-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUMA/NUMA1 Antibody (A02018-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nup37-picoband-trade-antibody-a11877-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11877-1-nup37-primary-antibodies-wb-testing-1.jpgAnti-NUP37 Antibody Picoband® Western blot analysis of NUP37 using anti-NUP37 antibody (A11877-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP37 antigen affinity purified polyclonal antibody (Catalog # A11877-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP37 at approximately 37 kDa. The expected band size for NUP37 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11877-1-nup37-primary-antibodies-ihc-testing-2.jpgAnti-NUP37 Antibody Picoband® IHC analysis of NUP37 using anti-NUP37 antibody (A11877-1). NUP37 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP37 Antibody (A11877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11877-1-nup37-primary-antibodies-ihc-testing-3.jpgAnti-NUP37 Antibody Picoband® IHC analysis of NUP37 using anti-NUP37 antibody (A11877-1). NUP37 was detected in a paraffin-embedded section of human large B-cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP37 Antibody (A11877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11877-1-nup37-primary-antibodies-ihc-testing-4.jpgAnti-NUP37 Antibody Picoband® IHC analysis of NUP37 using anti-NUP37 antibody (A11877-1). NUP37 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP37 Antibody (A11877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11877-1-nup37-primary-antibodies-ihc-testing-5.jpgAnti-NUP37 Antibody Picoband® IHC analysis of NUP37 using anti-NUP37 antibody (A11877-1). NUP37 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP37 Antibody (A11877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11877-1-nup37-primary-antibodies-if-testing-6.jpgAnti-NUP37 Antibody Picoband® IF analysis of NUP37 using anti-NUP37 antibody (A11877-1). NUP37 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP37 Antibody (A11877-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 594 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11877-1-nup37-primary-antibodies-fcm-testing-7.pngAnti-NUP37 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-NUP37 antibody (A11877-1). Overlay histogram showing MCF-7 cells stained with A11877-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUP37 Antibody (A11877-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nup54-picoband-trade-antibody-a10830-2-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10830-2-nup54-primary-antibodies-wb-testing-1.jpgAnti-NUP54 Antibody Picoband® Western blot analysis of NUP54 using anti-NUP54 antibody (A10830-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP54 antigen affinity purified polyclonal antibody (Catalog # A10830-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP54 at approximately 58 kDa. The expected band size for NUP54 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10830-2-nup54-primary-antibodies-ihc-testing-2.jpgAnti-NUP54 Antibody Picoband® IHC analysis of NUP54 using anti-NUP54 antibody (A10830-2). NUP54 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP54 Antibody (A10830-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10830-2-nup54-primary-antibodies-if-testing-3.jpgAnti-NUP54 Antibody Picoband® IF analysis of NUP54 using anti-NUP54 antibody (A10830-2). NUP54 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP54 Antibody (A10830-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 594 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10830-2-nup54-primary-antibodies-fcm-testing-4.pngAnti-NUP54 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-NUP54 antibody (A10830-2). Overlay histogram showing Hela cells stained with A10830-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUP54 Antibody (A10830-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nup107-picoband-trade-antibody-a03724-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03724-1-nup107-primary-antibodies-wb-testing-1.jpgAnti-NUP107 Antibody Picoband® Western blot analysis of NUP107 using anti-NUP107 antibody (A03724-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Colo320 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: human PC-3 whole cell lysates, Lane 6: human K562 whole cell lysates, Lane 7: human HEL whole cell lysates, Lane 8: rat PC-12 whole cell lysates, Lane 9: mouse testis tissue lysates, Lane 10: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP107 antigen affinity purified polyclonal antibody (Catalog # A03724-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP107 at approximately 106 kDa. The expected band size for NUP107 is at 106 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03724-1-nup107-primary-antibodies-if-testing-2.jpgAnti-NUP107 Antibody Picoband® IF analysis of NUP107 using anti-NUP107 antibody (A03724-1). NUP107 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP107 Antibody (A03724-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 594 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03724-1-nup107-primary-antibodies-fcm-testing-3.pngAnti-NUP107 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NUP107 antibody (A03724-1). Overlay histogram showing HEL cells stained with A03724-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUP107 Antibody (A03724-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03724-1-nup107-primary-antibodies-ip-testing-4.jpgAnti-NUP107 Antibody Picoband® Immunoprecipitating (IP) NUP107 in 293T whole cell lysate. Western blot analysis of NUP107 using anti-NUP107 antibody (A03724-1); Lane 1: 293T whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-NUP107 antibody in 293T whole cell lysate; Lane 3: anti-NUP107 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NUP107 antigen affinity purified polyclonal antibody (A03724-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NUP107 at approximately 106 kDa. The expected band size for NUP107 is at 106 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nup133-picoband-trade-antibody-a05327-2-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05327-2-nup133-primary-antibodies-wb-testing-1.jpgAnti-NUP133 Antibody Picoband® Western blot analysis of NUP133 using anti-NUP133 antibody (A05327-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: rat NRK whole cell lysates, Lane 6: mouse Neuro-2a whole cell lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP133 antigen affinity purified polyclonal antibody (Catalog # A05327-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP133 at approximately 129 kDa. The expected band size for NUP133 is at 129 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05327-2-nup133-primary-antibodies-if-testing-2.jpgAnti-NUP133 Antibody Picoband® IF analysis of NUP133 using anti-NUP133 antibody (A05327-2) and anti-Beta Tubulin antibody (M01857-3). NUP133 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP133 Antibody (A05327-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05327-2-nup133-primary-antibodies-if-testing-3.jpgAnti-NUP133 Antibody Picoband® IF analysis of NUP133 using anti-NUP133 antibody (A05327-2) and anti-Beta Tubulin antibody (M01857-3). NUP133 was detected in immunocytochemical section of C6 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP133 Antibody (A05327-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05327-2-nup133-primary-antibodies-ip-testing-4.jpgAnti-NUP133 Antibody Picoband® Immunoprecipitating NUP133 in Hela whole cell lysate . Western blot analysis of NUP133 using anti-NUP133 antibody (A05327-2). Lane 1: Hela whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-NUP133 antibody in Hela whole cell lysate. Lane 3: anti-NUP133 antibody (2μg) + Hela whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NUP133 antigen affinity purified polyclonal antibody (A05327-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NUP133 at approximately 129 kDa. The expected band size for NUP133 is at 129 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nup155-picoband-trade-antibody-a06391-2-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06391-2-nup155-primary-antibodies-wb-testing-1.jpgAnti-NUP155 Antibody Picoband® Western blot analysis of NUP155 using anti-NUP155 antibody (A06391-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human SiHa whole cell lysates, Lane 5: human K562 whole cell lysates, Lane 6: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP155 antigen affinity purified polyclonal antibody (Catalog # A06391-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP155 at approximately 140-150 kDa. The expected band size for NUP155 is at 140-150 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06391-2-nup155-primary-antibodies-if-testing-2.jpgAnti-NUP155 Antibody Picoband® IF analysis of NUP155 using anti-NUP155 antibody (A06391-2) and anti-Beta Tubulin antibody (M01857-3). NUP155 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP155 Antibody (A06391-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06391-2-nup155-primary-antibodies-fcm-testing-3.pngAnti-NUP155 Antibody Picoband® Flow Cytometry analysis of HELA cells using anti-NUP155 antibody (A06391-2). Overlay histogram showing HELA cells stained with A06391-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUP155 Antibody (A06391-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mgam-picoband-trade-antibody-a07347-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07347-mgam-primary-antibodies-wb-testing-1.jpgAnti-MGAM Antibody Picoband® Western blot analysis of MGAM using anti-MGAM antibody (A07347). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat small intestine lysates, Lane 2: mouse small intestine lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MGAM antigen affinity purified polyclonal antibody (Catalog # A07347) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MGAM at approximately 240 kDa. The expected band size for MGAM is at 210 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07347-mgam-primary-antibodies-ihc-testing-2.jpgAnti-MGAM Antibody Picoband® IHC analysis of MGAM using anti-MGAM antibody (A16132-1). MGAM was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGAM Antibody (A16132-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07347-mgam-primary-antibodies-ihc-testing-3.jpgAnti-MGAM Antibody Picoband® IHC analysis of MGAM using anti-MGAM antibody (A16132-1). MGAM was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGAM Antibody (A16132-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07347-mgam-primary-antibodies-fcm-testing-4.pngAnti-MGAM Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-MGAM antibody (A07347). Overlay histogram showing U20S cells stained with A07347 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MGAM Antibody (A07347, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nt5c-picoband-trade-antibody-a10650-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10650-1-nt5c-primary-antibodies-wb-testing-1.jpgAnti-NT5C Antibody Picoband® Western blot analysis of NT5C using anti-NT5C antibody (A10650-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human HL-60 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human A549 whole cell lysates, Lane 7: human U20S whole cell lysates, Lane 8: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NT5C antigen affinity purified polyclonal antibody (Catalog # A10650-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NT5C at approximately 24 kDa. The expected band size for NT5C is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10650-1-nt5c-primary-antibodies-ihc-testing-2.jpgAnti-NT5C Antibody Picoband® IHC analysis of NT5C using anti-NT5C antibody (A10650-1). NT5C was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NT5C Antibody (A10650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10650-1-nt5c-primary-antibodies-ihc-testing-3.jpgAnti-NT5C Antibody Picoband® IHC analysis of NT5C using anti-NT5C antibody (A10650-1). NT5C was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NT5C Antibody (A10650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10650-1-nt5c-primary-antibodies-ihc-testing-4.jpgAnti-NT5C Antibody Picoband® IHC analysis of NT5C using anti-NT5C antibody (A10650-1). NT5C was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NT5C Antibody (A10650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10650-1-nt5c-primary-antibodies-ihc-testing-5.jpgAnti-NT5C Antibody Picoband® IHC analysis of NT5C using anti-NT5C antibody (A10650-1). NT5C was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NT5C Antibody (A10650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10650-1-nt5c-primary-antibodies-fcm-testing-6.pngAnti-NT5C Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-NT5C antibody (A10650-1). Overlay histogram showing U251 cells stained with A10650-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NT5C Antibody (A10650-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mecr-picoband-trade-antibody-a08189-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08189-1-mecr-primary-antibodies-wb-testing-1.jpgAnti-MECR Antibody Picoband® Western blot analysis of MECR using anti-MECR antibody (A08189-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat stomach tissue lysates, Lane 4: rat heart tissue lysates, Lane 5: rat stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MECR antigen affinity purified polyclonal antibody (Catalog # A08189-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MECR at approximately 38 kDa. The expected band size for MECR is at38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08189-1-mecr-primary-antibodies-ihc-testing-2.jpgAnti-MECR Antibody Picoband® IHC analysis of MECR using anti-MECR antibody (A08189-1). MECR was detected in a paraffin-embedded section of human parotid acinar cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECR Antibody (A08189-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08189-1-mecr-primary-antibodies-ihc-testing-3.jpgAnti-MECR Antibody Picoband® IHC analysis of MECR using anti-MECR antibody (A08189-1). MECR was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECR Antibody (A08189-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08189-1-mecr-primary-antibodies-ihc-testing-4.jpgAnti-MECR Antibody Picoband® IHC analysis of MECR using anti-MECR antibody (A08189-1). MECR was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECR Antibody (A08189-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08189-1-mecr-primary-antibodies-fcm-testing-5.pngAnti-MECR Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MECR antibody (A08189-1). Overlay histogram showing 293T cells stained with A08189-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MECR Antibody (A08189-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-med26-picoband-trade-antibody-a09340-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09340-1-med26-primary-antibodies-wb-testing-1.jpgAnti-MED26 Antibody Picoband® Western blot analysis of MED26 using anti-MED26 antibody (A09340-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED26 antigen affinity purified polyclonal antibody (Catalog # A09340-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED26 at approximately 65 kDa. The expected band size for MED26 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09340-1-med26-primary-antibodies-ihc-testing-2.jpgAnti-MED26 Antibody Picoband® IHC analysis of MED26 using anti-MED26 antibody (A09340-1). MED26 was detected in a paraffin-embedded section of human parotid acinar cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED26 Antibody (A09340-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09340-1-med26-primary-antibodies-ihc-testing-3.jpgAnti-MED26 Antibody Picoband® IHC analysis of MED26 using anti-MED26 antibody (A09340-1). MED26 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED26 Antibody (A09340-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09340-1-med26-primary-antibodies-ihc-testing-4.jpgAnti-MED26 Antibody Picoband® IHC analysis of MED26 using anti-MED26 antibody (A09340-1). MED26 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED26 Antibody (A09340-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09340-1-med26-primary-antibodies-if-testing-5.jpgAnti-MED26 Antibody Picoband® IF analysis of MED26 using anti-MED26 antibody (A09340-1) and anti-Beta Tubulin antibody (M01857-3). MED26 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MED26 Antibody (A09340-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09340-1-med26-primary-antibodies-fcm-testing-6.pngAnti-MED26 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MED26 antibody (A09340-1). Overlay histogram showing 293T cells stained with A09340-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED26 Antibody (A09340-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nt5c1a-picoband-trade-antibody-a12036-2-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12036-2-nt5c1a-primary-antibodies-wb-testing-1.jpgAnti-NT5C1A Antibody Picoband® Western blot analysis of NT5C1A using anti-NT5C1A antibody (A12036-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NT5C1A antigen affinity purified polyclonal antibody (Catalog # A12036-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NT5C1A at approximately 41 kDa. The expected band size for NT5C1A is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12036-2-nt5c1a-primary-antibodies-ihc-testing-2.jpgAnti-NT5C1A Antibody Picoband® IHC analysis of NT5C1A using anti-NT5C1A antibody (A12036-2). NT5C1A was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NT5C1A Antibody (A12036-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-nr2c2-picoband-trade-antibody-a02752-2-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02752-2-nr2c2-primary-antibodies-wb-testing-1.jpgAnti-NR2C2 Antibody Picoband® Western blot analysis of NR2C2 using anti-NR2C2 antibody (A02752-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: monkey COS-7 whole cell lysates, Lane 6: human HEL whole cell lysates, Lane 7: human U20S whole cell lysates, Lane 8: human SH-SY5Y whole cell lysates, Lane 9: rat C6 whole cell lysates, Lane 10: mouse thymus tissue lysates, Lane 11: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR2C2 antigen affinity purified polyclonal antibody (Catalog # A02752-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NR2C2 at approximately 68 kDa. The expected band size for NR2C2 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02752-2-nr2c2-primary-antibodies-ihc-testing-2.jpgAnti-NR2C2 Antibody Picoband® IHC analysis of NR2C2 using anti-NR2C2 antibody (A02752-2). NR2C2 was detected in a paraffin-embedded section of human acinic cell carcinoma parotid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR2C2 Antibody (A02752-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02752-2-nr2c2-primary-antibodies-ihc-testing-3.jpgAnti-NR2C2 Antibody Picoband® IHC analysis of NR2C2 using anti-NR2C2 antibody (A02752-2). NR2C2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR2C2 Antibody (A02752-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02752-2-nr2c2-primary-antibodies-fcm-testing-4.pngAnti-NR2C2 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NR2C2 antibody (A02752-2). Overlay histogram showing 293T cells stained with A02752-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NR2C2 Antibody (A02752-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nr5a2-picoband-trade-antibody-a01332-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01332-1-nr5a2-primary-antibodies-wb-testing-1.jpgAnti-NR5A2 Antibody Picoband® Western blot analysis of NR5A2 using anti-NR5A2 antibody (A01332-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: human MCF-7 whole cell lysates, Lane 6: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR5A2 antigen affinity purified polyclonal antibody (Catalog # A01332-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NR5A2 at approximately 70 kDa. The expected band size for NR5A2 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01332-1-nr5a2-primary-antibodies-ihc-testing-2.jpgAnti-NR5A2 Antibody Picoband® IHC analysis of NR5A2 using anti-NR5A2 antibody (A01332-1). NR5A2 was detected in a paraffin-embedded section of human parotid acinar cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR5A2 Antibody (A01332-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01332-1-nr5a2-primary-antibodies-ihc-testing-3.jpgAnti-NR5A2 Antibody Picoband® IHC analysis of NR5A2 using anti-NR5A2 antibody (A01332-1). NR5A2 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR5A2 Antibody (A01332-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01332-1-nr5a2-primary-antibodies-ihc-testing-4.jpgAnti-NR5A2 Antibody Picoband® IHC analysis of NR5A2 using anti-NR5A2 antibody (A01332-1). NR5A2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR5A2 Antibody (A01332-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01332-1-nr5a2-primary-antibodies-fcm-testing-5.pngAnti-NR5A2 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-NR5A2 antibody (A01332-1). Overlay histogram showing CACO-2 cells stained with A01332-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NR5A2 Antibody (A01332-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nrd1-nrdc-picoband-trade-antibody-a05739-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05739-1-nrdc-primary-antibodies-wb-testing-1_1.jpgAnti-NRD1/NRDC Antibody Picoband®Western blot analysis of NRD1/NRDC using anti-NRD1/NRDC antibody (A05739-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NRD1/NRDC antigen affinity purified polyclonal antibody (A05739-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NRD1/NRDC at approximately 140 kDa. The expected band size for NRD1/NRDC is at 132 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05739-1-nrdc-primary-antibodies-fcm-testing-2.pngAnti-NRD1/NRDC Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-NRD1/NRDC antibody (A05739-1). Overlay histogram showing MCF-7 cells stained with A05739-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NRD1/NRDC Antibody (A05739-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nsmce2-picoband-trade-antibody-a06693-1-boster.html2026-04-04T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06693-1-nsmce2-primary-antibodies-wb-testing-1_1.jpgAnti-NSMCE2 Antibody Picoband® Western blot analysis of NSMCE2 using anti-NSMCE2 antibody (A06693-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSMCE2 antigen affinity purified polyclonal antibody (Catalog # A06693-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSMCE2 at approximately 34 kDa. The expected band size for NSMCE2 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06693-1-nsmce2-primary-antibodies-ip-testing-3.jpgAnti-NSMCE2 Antibody Picoband® Immunoprecipitating NSMCE2 in MCF-7 whole cell lysate. Western blot analysis of NSMCE2 using anti-NSMCE2 antibody (A02215-2). Lane 1: MCF-7 whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-NSMCE2 antibody in MCF-7 whole cell lysate. Lane 3: anti-NSMCE2 antibody (2μg) + MCF-7 whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NSMCE2 antigen affinity purified polyclonal antibody (A02215-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NSMCE2 at approximately 34 kDa. The expected band size for NSMCE2 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06693-1-nsmce2-primary-antibodies-if-testing-2.jpgAnti-NSMCE2 Antibody Picoband® IF analysis of NSMCE2 using anti-NSMCE2 antibody (A06693-1) and anti-Beta Tubulin antibody (M01857-3). NSMCE2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NSMCE2 Antibody (A06693-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06693-1-nsmce2-primary-antibodies-fcm-testing-4.jpgAnti-NSMCE2 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-NSMCE2 antibody (A06693-1). Overlay histogram showing PC-3 cells stained with A06693-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSMCE2 Antibody (A06693-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-nelf-nsmf-picoband-trade-antibody-a08385-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08385-1-nsmf-primary-antibodies-wb-testing-1_1.jpgAnti-NELF/NSMF Antibody Picoband® Western blot analysis of NELF/NSMF using anti-NELF/NSMF antibody (A08385-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat RH35 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse HEPA1-6 whole cell lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NELF/NSMF antigen affinity purified polyclonal antibody (Catalog # A08385-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NELF/NSMF at approximately 44,60 kDa. The expected band size for NELF/NSMF is at 44,60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08385-1-nsmf-primary-antibodies-ihc-testing-2.jpgAnti-NELF/NSMF Antibody Picoband® IHC analysis of NELF/NSMF using anti-NELF/NSMF antibody (A08385-1). NELF/NSMF was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NELF/NSMF Antibody (A08385-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08385-1-nsmf-primary-antibodies-fcm-testing-3.pngAnti-NELF/NSMF Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-NELF/NSMF antibody (A08385-1). Overlay histogram showing Hela cells stained with A08385-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NELF/NSMF Antibody (A08385-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nsun2-picoband-trade-antibody-a03878-1-boster.html2026-03-17T05:15:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-wb-testing-1.jpgAnti-NSUN2 Antibody Picoband® Western blot analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSUN2 antigen affinity purified polyclonal antibody (Catalog # A03878-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSUN2 at approximately 100 kDa. The expected band size for NSUN2 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-ihc-testing-2.jpgAnti-NSUN2 Antibody Picoband® IHC analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). NSUN2 was detected in a paraffin-embedded section of human acinic cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN2 Antibody (A03878-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-ihc-testing-3.jpgAnti-NSUN2 Antibody Picoband® IHC analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). NSUN2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN2 Antibody (A03878-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-ihc-testing-4.jpgAnti-NSUN2 Antibody Picoband® IHC analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). NSUN2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN2 Antibody (A03878-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-ihc-testing-5.jpgAnti-NSUN2 Antibody Picoband® IHC analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). NSUN2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN2 Antibody (A03878-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-ihc-testing-6.jpgAnti-NSUN2 Antibody Picoband® IHC analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). NSUN2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN2 Antibody (A03878-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-ihc-testing-7.jpgAnti-NSUN2 Antibody Picoband® IHC analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). NSUN2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN2 Antibody (A03878-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-ihc-testing-8.jpgAnti-NSUN2 Antibody Picoband® IHC analysis of NSUN2 using anti-NSUN2 antibody (A03878-1). NSUN2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN2 Antibody (A03878-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-fcm-testing-9.pngAnti-NSUN2 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NSUN2 antibody (A03878-1). Overlay histogram showing 293T cells stained with A03878-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSUN2 Antibody (A03878-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03878-1-nsun2-primary-antibodies-if-testing-10.jpgAnti-NSUN2 Antibody Picoband® IF analysis of NSUN2 using anti-NSUN2 antibody (A03878-1) and anti-Tubulin Alpha antibody (M03989-3). NSUN2 was detected in immunocytochemical section of NRK cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NSUN2 Antibody (A03878-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-nsun3-picoband-trade-antibody-a16002-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16002-nsun3-primary-antibodies-wb-testing-1_.jpgAnti-NSUN3 Antibody Picoband® Western blot analysis of NSUN3 using anti-NSUN3 antibody (A16002). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates, Lane 2: monkey COS-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSUN3 antigen affinity purified polyclonal antibody (Catalog # A16002) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSUN3 at approximately 38 kDa. The expected band size for NSUN3 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16002-nsun3-primary-antibodies-fcm-testing-2.pngAnti-NSUN3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-NSUN3 antibody (A16002). Overlay histogram showing U251 cells stained with A16002 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSUN3 Antibody (A16002, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nudt5-picoband-trade-antibody-a07530-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07530-nudt5-primary-antibodies-wb-testing-1_1.jpgAnti-NUDT5 Antibody Picoband® Western blot analysis of NUDT5 using anti-NUDT5 antibody (A07530). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human CACO-2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse HEPA1/6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT5 antigen affinity purified polyclonal antibody (Catalog # A07530) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDT5 at approximately 35 kDa. The expected band size for NUDT5 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07530-nudt5-primary-antibodies-ihc-testing-2_1.jpgAnti-NUDT5 Antibody Picoband® IHC analysis of NUDT5 using anti-NUDT5 antibody (A07530). NUDT5 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT5 Antibody (A07530) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07530-nudt5-primary-antibodies-ihc-testing-3_1.jpgAnti-NUDT5 Antibody Picoband® IHC analysis of NUDT5 using anti-NUDT5 antibody (A07530). NUDT5 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT5 Antibody (A07530) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07530-nudt5-primary-antibodies-ihc-testing-4.jpgAnti-NUDT5 Antibody Picoband® IHC analysis of NUDT5 using anti-NUDT5 antibody (A07530). NUDT5 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT5 Antibody (A07530) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07530-nudt5-primary-antibodies-fcm-testing-5.jpgAnti-NUDT5 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-NUDT5 antibody (A07530). Overlay histogram showing CACO-2 cells stained with A07530 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDT5 Antibody (A07530, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07530-nudt5-primary-antibodies-if-testing-6.jpgAnti-NUDT5 Antibody Picoband® IF analysis of NUDT5 using anti-NUDT5 antibody (A07530) and anti-Beta Tubulin antibody (M01857-3). NUDT5 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUDT5 Antibody (A07530) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07530-nudt5-primary-antibodies-ip-testing-7.jpgAnti-NUDT5 Antibody Picoband® Immunoprecipitating NUDT5 in 293T whole cell lysate. Western blot analysis of NUDT5 using anti-NUDT5 antibody (A07530); Lane 1: 293T whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-NUDT5 antibody in 293T whole cell lysate; Lane 3: anti-NUDT5 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NUDT5 antigen affinity purified polyclonal antibody (A07530) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NUDT5 at approximately 35 kDa. The expected band size for NUDT5 is at 24 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nudt6-picoband-trade-antibody-a08301-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08301-1-nudt6-primary-antibodies-wb-testing-1.jpgAnti-NUDT6 Antibody Picoband® Western blot analysis of NUDT6 using anti-NUDT6 antibody (A08301-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human THP-1 whole cell lysates, Lane 5: human PC-3 whole cell lysates, Lane 6: human A549 whole cell lysates, Lane 7: human Hela whole cell lysates, Lane 8: human SH-SY5Y whole cell lysates, Lane 9: rat kidney tissue lysates, Lane 10: rat H9C2 whole cell lysates, Lane 11: mouse kidney tissue lysates, Lane 12: mouse HEPA1/6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT6 antigen affinity purified polyclonal antibody (Catalog # A08301-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDT6 at approximately 72 kDa. The expected band size for NUDT6 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08301-1-nudt6-primary-antibodies-ihc-testing-2.jpgAnti-NUDT6 Antibody Picoband® IHC analysis of NUDT6 using anti-NUDT6 antibody (A08301-1). NUDT6 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT6 Antibody (A08301-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08301-1-nudt6-primary-antibodies-ihc-testing-3.jpgAnti-NUDT6 Antibody Picoband® IHC analysis of NUDT6 using anti-NUDT6 antibody (A08301-1). NUDT6 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT6 Antibody (A08301-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-nupl2-nup42-picoband-trade-antibody-a09480-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09480-nupl2-primary-antibodies-wb-testing-1.jpgAnti-NUPL2/NUP42 Antibody Picoband® Western blot analysis of NUPL2/NUP42 using anti-NUPL2/NUP42 antibody (A09480). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUPL2/NUP42 antigen affinity purified polyclonal antibody (Catalog # A09480) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUPL2/NUP42 at approximately 36 kDa. The expected band size for NUPL2/NUP42 is at 36 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-mad2l1bp-picoband-trade-antibody-a06825-2-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06825-2-mad2l1bp-primary-antibodies-wb-testing-1.jpgAnti-MAD2L1BP Antibody Picoband® Western blot analysis of MAD2L1BP using anti-MAD2L1BP antibody (A06825-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human THP-1 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human HEL whole cell lysates, Lane 7: human 293T whole cell lysates, Lane 8: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAD2L1BP antigen affinity purified polyclonal antibody (Catalog # A06825-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAD2L1BP at approximately 37 kDa. The expected band size for MAD2L1BP is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06825-2-mad2l1bp-primary-antibodies-fcm-testing-2.pngAnti-MAD2L1BP Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-MAD2L1BP antibody (A06825-2). Overlay histogram showing HEL cells stained with A06825-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAD2L1BP Antibody (A06825-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mad2l2-picoband-trade-antibody-a02357-4-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02357-4-mad2l2-primary-antibodies-wb-testing-1.jpgAnti-MAD2L2 Antibody Picoband® Western blot analysis of MAD2L2 using anti-MAD2L2 antibody (A02357-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human Jurkat whole cell lysates, Lane 6: human THP-1 whole cell lysates, Lane 7: human SH-SY5Y whole cell lysats. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAD2L2 antigen affinity purified polyclonal antibody (Catalog # A02357-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAD2L2 at approximately 24 kDa. The expected band size for MAD2L2 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02357-4-mad2l2-primary-antibodies-ihc-testing-2.jpgAnti-MAD2L2 Antibody Picoband® IHC analysis of MAD2L2 using anti-MAD2L2 antibody (A02357-4). MAD2L2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAD2L2 Antibody (A02357-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02357-4-mad2l2-primary-antibodies-if-testing-3.jpgAnti-MAD2L2 Antibody Picoband® IF analysis of MAD2L2 using anti-MAD2L2 antibody (A02357-4). MAD2L2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAD2L2 Antibody (A02357-4) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02357-4-mad2l2-primary-antibodies-fcm-testing-4.pngAnti-MAD2L2 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MAD2L2 antibody (A02357-4). Overlay histogram showing Hela cells stained with A02357-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAD2L2 Antibody (A02357-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-maea-picoband-trade-antibody-a08766-2-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08766-2-maea-primary-antibodies-wb-testing-1.jpgAnti-MAEA Antibody Picoband® Western blot analysis of MAEA using anti-MAEA antibody (A08766-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat PC-12 whole cell lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAEA antigen affinity purified polyclonal antibody (Catalog # A08766-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAEA at approximately 45 kDa. The expected band size for MAEA is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08766-2-maea-primary-antibodies-fcm-testing-2.pngAnti-MAEA Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-MAEA antibody (A08766-2). Overlay histogram showing U251 cells stained with A08766-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAEA Antibody (A08766-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mael-picoband-trade-antibody-a08829-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08829-1-mael-primary-antibodies-wb-testing-1.jpgAnti-MAEL Antibody Picoband® Western blot analysis of MAEL using anti-MAEL antibody (A08829-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAEL antigen affinity purified polyclonal antibody (Catalog # A08829-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAEL at approximately 49 kDa. The expected band size for MAEL is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08829-1-mael-primary-antibodies-fcm-testing-2.pngAnti-MAEL Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-MAEL antibody (A08829-1). Overlay histogram showing U251 cells stained with A08829-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAEL Antibody (A08829-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-magec3-picoband-trade-antibody-a16360-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16360-1-maegc3-primary-antibodies-wb-testing-1.jpgAnti-MAGEC3 Antibody Picoband® Western blot analysis of MAGEC3 using anti-MAGEC3 antibody (A16360-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAGEC3 antigen affinity purified polyclonal antibody (Catalog # A16360-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAGEC3 at approximately 72 kDa. The expected band size for MAGEC3 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16360-1-maegc3-primary-antibodies-fcm-testing-2.pngAnti-MAGEC3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-MAGEC3 antibody (A16360-1). Overlay histogram showing U251 cells stained with A16360-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAGEC3 Antibody (A16360-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mark3-picoband-trade-antibody-a05355-2-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05355-2-mark3-primary-antibodies-wb-testing-1_1.jpgAnti-MARK3 Antibody Picoband® Western blot analysis of MARK3 using anti-MARK3 antibody (A05355-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat NRK whole cell lysates, Lane 4: mouse EL-4 whole cell lysates, Lane 5: mouse 4T1 whole cell lysates, Lane 6: mouse J774A.1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MARK3 antigen affinity purified polyclonal antibody (Catalog # A05355-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MARK3 at approximately 80 kDa. The expected band size for MARK3 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05355-2-mark3-primary-antibodies-ihc-testing-2.jpgAnti-MARK3 Antibody Picoband® IHC analysis of MARK3 using anti-MARK3 antibody (A05355-2). MARK3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MARK3 Antibody (A05355-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05355-2-mark3-primary-antibodies-ihc-testing-3.jpgAnti-MARK3 Antibody Picoband® IHC analysis of MARK3 using anti-MARK3 antibody (A05355-2). MARK3 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MARK3 Antibody (A05355-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05355-2-mark3-primary-antibodies-ihc-testing-4.jpgAnti-MARK3 Antibody Picoband® IHC analysis of MARK3 using anti-MARK3 antibody (A05355-2). MARK3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MARK3 Antibody (A05355-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05355-2-mark3-primary-antibodies-ihc-testing-5.jpgAnti-MARK3 Antibody Picoband® IHC analysis of MARK3 using anti-MARK3 antibody (A05355-2). MARK3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MARK3 Antibody (A05355-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05355-2-mark3-primary-antibodies-fcm-testing-6.pngAnti-MARK3 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MARK3 antibody (A05355-2). Overlay histogram showing 293T cells stained with A05355-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MARK3 Antibody (A05355-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mars2-picoband-trade-antibody-a10675-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10675-mars2-primary-antibodies-wb-testing-1.jpgAnti-MARS2 Antibody Picoband® Western blot analysis of MARS2 using anti-MARS2 antibody (A10675). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates, Lane 8: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MARS2 antigen affinity purified polyclonal antibody (Catalog # A10675) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MARS2 at approximately 70 kDa. The expected band size for MARS2 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10675-mars2-primary-antibodies-if-testing-1.jpgAnti-MARS2 Antibody Picoband®IF analysis of MARS2 using anti-MARS2 antibody (A10675). MARS2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MARS2 Antibody (A10675) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-med17-picoband-trade-antibody-a05399-2-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05399-2-med17-primary-antibodies-wb-testing-1.jpgAnti-MED17 Antibody Picoband® Western blot analysis of MED17 using anti-MED17 antibody (A05399-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED17 antigen affinity purified polyclonal antibody (Catalog # A05399-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED17 at approximately 73 kDa. The expected band size for MED17 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05399-2-med17-primary-antibodies-fcm-testing-2.pngAnti-MED17 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-MED17 antibody (A05399-2). Overlay histogram showing U251 cells stained with A05399-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED17 Antibody (A05399-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mfap3-picoband-trade-antibody-a13942-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13942-mfap3-primary-antibodies-wb-testing-1.jpgAnti-MFAP3 Antibody Picoband® Western blot analysis of MFAP3 using anti-MFAP3 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MFAP3 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MFAP3 at approximately 45-50 kDa. The expected band size for MFAP3 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13942-mfap3-primary-antibodies-ihc-testing-2.jpgAnti-MFAP3 Antibody Picoband® IHC analysis of MFAP3 using anti-MFAP3 antibody (A13942). MFAP3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MFAP3 Antibody (A13942) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13942-mfap3-primary-antibodies-ihc-testing-3.jpgAnti-MFAP3 Antibody Picoband® IHC analysis of MFAP3 using anti-MFAP3 antibody (A13942). MFAP3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MFAP3 Antibody (A13942) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13942-mfap3-primary-antibodies-ihc-testing-4.jpgAnti-MFAP3 Antibody Picoband® IHC analysis of MFAP3 using anti-MFAP3 antibody (A13942). MFAP3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MFAP3 Antibody (A13942) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13942-mfap3-primary-antibodies-ihc-testing-5.jpgAnti-MFAP3 Antibody Picoband® IHC analysis of MFAP3 using anti-MFAP3 antibody (A13942). MFAP3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MFAP3 Antibody (A13942) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13942-mfap3-primary-antibodies-fcm-testing-6.pngAnti-MFAP3 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MFAP3 antibody (A13942). Overlay histogram showing 293T cells stained with A13942 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MFAP3 Antibody (A13942, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mgat2-picoband-trade-antibody-a06432-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06432-1-mgat2-primary-antibodies-wb-testing-1.jpgAnti-MGAT2 Antibody Picoband® Western blot analysis of MGAT2 using anti-MGAT2 antibody (A06432-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MGAT2 antigen affinity purified polyclonal antibody (Catalog # A06432-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MGAT2 at approximately 50 kDa. The expected band size for MGAT2 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06432-1-mgat2-primary-antibodies-ihc-testing-2.jpgAnti-MGAT2 Antibody Picoband® IHC analysis of MGAT2 using anti-MGAT2 antibody (A06432-1). MGAT2 was detected in a paraffin-embedded section of human large B-cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGAT2 Antibody (A06432-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06432-1-mgat2-primary-antibodies-ihc-testing-3.jpgAnti-MGAT2 Antibody Picoband® IHC analysis of MGAT2 using anti-MGAT2 antibody (A06432-1). MGAT2 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGAT2 Antibody (A06432-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06432-1-mgat2-primary-antibodies-fcm-testing-4.pngAnti-MGAT2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MGAT2 antibody (A06432-1). Overlay histogram showing HepG2 cells stained with A06432-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MGAT2 Antibody (A06432-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mgat3-picoband-trade-antibody-a08470-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08470-1-mgat3-primary-antibodies-wb-testing-1.jpgAnti-MGAT3 Antibody Picoband® Western blot analysis of MGAT3 using anti-MGAT3 antibody (A08470-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MGAT3 antigen affinity purified polyclonal antibody (Catalog # A08470-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MGAT3 at approximately 61 kDa. The expected band size for MGAT3 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08470-1-mgat3-primary-antibodies-ihc-testing-2.jpgAnti-MGAT3 Antibody Picoband® IHC analysis of MGAT3 using anti-MGAT3 antibody (A08470-1). MGAT3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGAT3 Antibody (A08470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-mgat4b-picoband-trade-antibody-a10339-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10339-mgat4b-primary-antibodies-wb-testing-1.jpgAnti-MGAT4B Antibody Picoband® Western blot analysis of MGAT4B using anti-MGAT4B antibody (A10339). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MGAT4B antigen affinity purified polyclonal antibody (Catalog # A10339) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MGAT4B at approximately 70 kDa. The expected band size for MGAT4B is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10339-mgat4b-primary-antibodies-ihc-testing-2.jpgAnti-MGAT4B Antibody Picoband® IHC analysis of MGAT4B using anti-MGAT4B antibody (A10339). MGAT4B was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGAT4B Antibody (A10339) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-mgme1-picoband-trade-antibody-a09360-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09360-1-mgme1-primary-antibodies-wb-testing-1.jpgAnti-MGME1 Antibody Picoband® Western blot analysis of MGME1 using anti-MGME1 antibody (A09360-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MGME1 antigen affinity purified polyclonal antibody (Catalog # A09360-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MGME1 at approximately 36 kDa. The expected band size for MGME1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09360-1-mgme1-primary-antibodies-ihc-testing-2.jpgAnti-MGME1 Antibody Picoband® IHC analysis of MGME1 using anti-MGME1 antibody (A09360-1). MGME1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGME1 Antibody (A09360-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09360-1-mgme1-primary-antibodies-ihc-testing-3.jpgAnti-MGME1 Antibody Picoband® IHC analysis of MGME1 using anti-MGME1 antibody (A09360-1). MGME1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGME1 Antibody (A09360-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09360-1-mgme1-primary-antibodies-ihc-testing-4.jpgAnti-MGME1 Antibody Picoband® IHC analysis of MGME1 using anti-MGME1 antibody (A09360-1). MGME1 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MGME1 Antibody (A09360-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09360-1-mgme1-primary-antibodies-if-testing-5.jpgAnti-MGME1 Antibody Picoband® IF analysis of MGME1 using anti-MGME1 antibody (A09360-1). MGME1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MGME1 Antibody (A09360-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-mia3-picoband-trade-antibody-a06158-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06158-1-mia3-primary-antibodies-wb-testing-1.jpgAnti-MIA3 Antibody Picoband® Western blot analysis of MIA3 using anti-MIA3 antibody (A06158-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIA3 antigen affinity purified polyclonal antibody (Catalog # A06158-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIA3 at approximately 300 kDa. The expected band size for MIA3 is at 300 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06158-1-mia3-primary-antibodies-ihc-testing-2.jpgAnti-MIA3 Antibody Picoband® IHC analysis of MIA3 using anti-MIA3 antibody (A06158-1). MIA3 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIA3 Antibody (A06158-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06158-1-mia3-primary-antibodies-ihc-testing-3.jpgAnti-MIA3 Antibody Picoband® IHC analysis of MIA3 using anti-MIA3 antibody (A06158-1). MIA3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIA3 Antibody (A06158-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06158-1-mia3-primary-antibodies-ihc-testing-4.jpgAnti-MIA3 Antibody Picoband® IHC analysis of MIA3 using anti-MIA3 antibody (A06158-1). MIA3 was detected in a paraffin-embedded section of human testicular germ cell tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIA3 Antibody (A06158-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06158-1-mia3-primary-antibodies-if-testing-5.jpgAnti-MIA3 Antibody Picoband® IF analysis of MIA3 using anti-MIA3 antibody (A06158-1). MIA3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MIA3 Antibody (A06158-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06158-1-mia3-primary-antibodies-fcm-testing-6.pngAnti-MIA3 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MIA3 antibody (A06158-1). Overlay histogram showing 293T cells stained with A06158-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MIA3 Antibody (A06158-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®MIA3 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-micall2-picoband-trade-antibody-a12852-1-boster.html2026-03-17T05:15:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12852-1-micall2-primary-antibodies-wb-testing-1.jpgAnti-MICALL2 Antibody Picoband® Western blot analysis of MICALL2 using anti-MICALL2 antibody (A12852-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MICALL2 antigen affinity purified polyclonal antibody (Catalog # A12852-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MICALL2 at approximately 109 kDa. The expected band size for MICALL2 is at 109 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12852-1-micall2-primary-antibodies-ihc-testing-2.jpgAnti-MICALL2 Antibody Picoband® IHC analysis of MICALL2 using anti-MICALL2 antibody (A12852-1). MICALL2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL2 Antibody (A12852-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12852-1-micall2-primary-antibodies-fcm-testing-3.pngAnti-MICALL2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-MICALL2 antibody (A12852-1). Overlay histogram showing K562 cells stained with A12852-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MICALL2 Antibody (A12852-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-miga1-picoband-trade-antibody-a32472-boster.html2026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32472-miga1-primary-antibodies-wb-testing-1.jpgAnti-MIGA1 Antibody Picoband® Western blot analysis of MIGA1 using anti-MIGA1 antibody (A32472). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIGA1 antigen affinity purified polyclonal antibody (Catalog # A32472) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIGA1 at approximately 71 kDa. The expected band size for MIGA1 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32472-miga1-primary-antibodies-fcm-testing-2.pngAnti-MIGA1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-MIGA1 antibody (A32472). Overlay histogram showing U251 cells stained with A32472 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MIGA1 Antibody (A32472, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-f4-80-adgre1-picoband-trade-antibody-a08751-boster.html2026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-13020_2021_562_fig8_html.pngAnti-F4/80/Adgre1 AntibodyPseudoephedrine + emodin inhibited (M1) macrophage and activated (M2) macrophage in LPS‐induced rats lung tissue. A F4/80 expression was determined using immunohistochemistry (n = 3). B F4/80 positive score was determined using ImageJ: negative (0), low positive (1+), positive (2+), high positive (3+). C – F CD86, CD206 expression was determined using immunofluorescence (n = 5). Data are expressed as mean ± S.D. ## p < 0.01, ### p < 0.001 vs. control group. **p < 0.01, ***p < 0.001 vs. LPS alone group. +++ p < 0.001 vs. combined treatment group (20 + 40 mg/kg) Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s13020-021-00562-8'>35123524</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-ihc-testing-1.jpgAnti-F4/80/Adgre1 Antibody IHC analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-oncotarget-08-39356-g002.jpgAnti-F4/80/Adgre1 AntibodyADCP assays with BMDMs. In vitro assay to determine elimination of Raji cells by macrophages. (A) BMDMs from WT and FcαRI Tg C57BL/6 mice were incubated with CFSE-labeled Raji cells at an E:T ratio of 5:1 in the presence of 10 μg/mL anti-CD20 antibodies. After a 4-h incubation, cells were transferred to a new tube and visualized via confocal microscopy. Representative images of ADCP mediated by anti-CD20 antibodies are shown. (B) BMDMs were labeled with APC-F4/80 antibodies and cocultured with CFSE-labeled Raji cells in the presence of the indicated antibodies. Phagocytosis of Raji cells was analyzed by FACS and quantified as the percentage of double-positive cells relative to total CFSE-positive cells and F4/80+cells. ** P < 0.01 using unpaired two-tailed t tests. Index in PubMed under a CC BY license. PMID: <a href='https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503618/'>28454118</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-ihc-testing-2.jpgAnti-F4/80/Adgre1 Antibody IHC analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-41598_2024_69284_fig8_html.pngAnti-F4/80/Adgre1 AntibodySPP1+ macrophages were increased in SkM of the aging mice model, and senolytics decreased its proportion in vivo. ( A ) The diagram presents the experimental process. ( B – E ) Illustration of the gastrocnemius, quadriceps, tibialis anterior, and soleus in young, Old-Veh, and Old-DQ male mice group ( B ). Comparison of body weight ( C ), lean mass percentage ( D ), and quadriceps muscle weight ( E ) between distinct groups (n = 3 per group). ( F ) IF pictures of quadriceps cross-sections stained for Laminin in different groups. ( G ) Confocal microscopy of quadriceps IF staining exhibited F4/80 (green) positive and SPP1 (red) double positive (yellow arrows) SPP1+ macrophages in quadriceps of different groups (n = 3 per group). IF, immunofluorescence. SkM, skeletal muscle. Ns, no significant *, **, *** represent p value less than 0.05, 0.01, 0.001 respectively. Y, young; O, old. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41598-024-69284-9'>39103421</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-ihc-testing-3.jpgAnti-F4/80/Adgre1 Antibody IHC analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-10020_2025_1153_fig7_html.jpgAnti-F4/80/Adgre1 AntibodyEffects of co-adjustment of TO901317 and tacrolimus on AR following liver transplantation in rats. A – D Hepatic pathological changes and apoptosis following co-adjustment with TO901317 and tacrolimus during AR (magnification, ×200; scale bar = 100 μm) (The area indicated by the red arrow shows inflammatory cell infiltration in the portal area and hepatic sinusoids, cholangitis and venulitis, as well as hepatic parenchymal cell damage). E , F The percentages of M1-type polarized macrophages in different groups were detected by flow cytometry, macrophages were separated with FITC-labeled F4/80, and M1-type polarization was separated with PE-labeled CD86. G ALT and AST levels in rat serum. H Survival rate of rats. n = 6 for each group. I Levels of TNF-α IL-6 and IL-1β in serum of different groups. Differences among groups were assessed by one-way ANOVA. n = 6, ns P > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001 Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11908107/'>40087552</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-if-testing-4.jpgAnti-F4/80/Adgre1 Antibody IF analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-10020_2025_1153_fig6_html.jpgAnti-F4/80/Adgre1 AntibodyLXRα improves AR after liver transplantation by activating PI3K/AKT/mTOR pathway to regulate macrophage polarization. A , B Protein expression levels of PI3K/AKT/mTOR signaling pathway factors. C , D Detection of the proportion of M1 polarization by flow cytometry, macrophages were separated with FITC-labeled F4/80, and M1-type polarization was separated with PE-labeled CD86. E , F Pathological changes in the liver following treatment with TO901317 or LY294002 during AR (magnification, ×200; scale bar = 100 μm) (The area indicated by the red arrow shows inflammatory cell infiltration in the portal area and hepatic sinusoids, cholangitis and venulitis, as well as hepatic parenchymal cell damage). One-way ANOVA was used to determine the statistical differences between groups. n = 6, *P < 0.05, **P < 0.01, ***P < 0.001 Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11908107/'>40087552</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-if-testing-5.jpgAnti-F4/80/Adgre1 Antibody IF analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-10020_2025_1153_fig5_html.jpgAnti-F4/80/Adgre1 AntibodyEffects of ABCA1 in vivo. A , B Pathological changes in the liver following treatment with TO901317 and ABCA1 shRNA during AR (magnification, ×200/400; scale bar = 100 μm) (The area indicated by the red arrow shows inflammatory cell infiltration in the portal area and hepatic sinusoids, cholangitis and venulitis, as well as hepatic parenchymal cell damage). C , D Hepatic apoptosis following treatment with TO901317 and ABCA1 shRNA during AR (magnification, ×200; scale bar = 100 mm). E , F Protein expression levels of LXRα/ABCA1/MAPK and mTOR signaling pathway factors. E Detection of the proportion of M1 polarization by flow cytometry, macrophages were separated with FITC-labeled F4/80, and M1-type polarization was separated with PE-labeled CD86. One-way ANOVA was used to determine the statistical differences between groups. n = 6, ns P > 0.05, *P < 0.05, **P < 0.01, ***P < 0.001 Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC11908107/'>40087552</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-if-testing-6.jpgAnti-F4/80/Adgre1 Antibody IF analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-ihc-testing-4.jpgAnti-F4/80/Adgre1 AntibodyIHC analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08751-f4-primary-antibodies-ihc-testing-5.jpgAnti-F4/80/Adgre1 Antibody IHC analysis of F4/80/Adgre1 using anti-F4/80/Adgre1 antibody (A08751). F4/80/Adgre1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-F4/80/Adgre1 Antibody (A08751) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1238702026-03-10T04:35:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2252.jpgHuman MSR ELISA Kit PicoKine®Human MSR PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1238712026-03-10T04:35:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2253.pngHuman MYDGF ELISA Kit PicoKine®Human MYDGF PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1238722026-03-10T04:35:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek0579.pngHuman LIF ELISA Kit PicoKine®Human LIF PicoKine ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-nnp-1-antibody-dz41437-boster.html2026-03-10T04:35:49+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-cg6937-antibody-dz41438-boster.html2026-03-10T04:35:49+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-kif5aa-frameshift-antibody-dz41430-boster.html2026-03-17T05:15:07+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-tea-antibody-dz41433-boster.html2026-03-10T04:35:49+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-non3-antibody-dz41436-boster.html2026-03-10T04:35:49+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-starfish-tropomyosin-pan-variant1-5-antibody-dz41442-boster.html2026-03-10T04:35:49+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-starfish-tropomyosin-long-isoform-antibody-dz41443-boster.html2026-03-10T04:35:49+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238812026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04428-1-ifit2-primary-antibodies-wb-testing-1.jpgAnti-IFIT2 Antibody Picoband®Western blot analysis of IFIT2 using anti-IFIT2 antibody (A04428-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFIT2 antigen affinity purified polyclonal antibody (A04428-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IFIT2 at approximately 55 kDa. The expected band size for IFIT2 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04428-1-ifit2-primary-antibodies-ihc-testing-1.jpgAnti-IFIT2 Antibody Picoband®IHC analysis of IFIT2 using anti-IFIT2 antibody (A04428-1). IFIT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFIT2 Antibody (A04428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04428-1-ifit2-primary-antibodies-ihc-testing-2.jpgAnti-IFIT2 Antibody Picoband®IHC analysis of IFIT2 using anti-IFIT2 antibody (A04428-1). IFIT2 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFIT2 Antibody (A04428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04428-1-ifit2-primary-antibodies-ihc-testing-3.jpgAnti-IFIT2 Antibody Picoband®IHC analysis of IFIT2 using anti-IFIT2 antibody (A04428-1). IFIT2 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFIT2 Antibody (A04428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04428-1-ifit2-primary-antibodies-if-testing-1.jpgAnti-IFIT2 Antibody Picoband®IF analysis of IFIT2 using anti-IFIT2 antibody (A04428-1). IFIT2 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IFIT2 Antibody (A04428-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04428-1-ifit2-primary-antibodies-fcm-testing-1.jpgAnti-IFIT2 Antibody Picoband®Flow Cytometry analysis of SiHa cells using anti-IFIT2 antibody (A04428-1). Overlay histogram showing SiHa cells stained with A04428-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFIT2 Antibody (A04428-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1238822026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238832026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238842026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238852026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06541-2-fsp1-aifm2-primary-antibodies-wb-testing-1.jpgAnti-FSP1/AIFM2 Antibody Western blot analysis of FSP1/AIFM2 using anti-FSP1/AIFM2 antibody (A06541-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FSP1/AIFM2 antigen affinity purified polyclonal antibody (A06541-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FSP1/AIFM2 at approximately 41 kDa. The expected band size for FSP1/AIFM2 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06541-2-aifm2-primary-antibodies-ihc-testing-1.jpgAnti-FSP1/AIFM2 AntibodyIHC analysis of FSP1/AIFM2 using anti-FSP1/AIFM2 antibody (A06541-2). FSP1/AIFM2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FSP1/AIFM2 Antibody (A06541-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06541-2-aifm2-primary-antibodies-ihc-testing-2.jpgAnti-FSP1/AIFM2 AntibodyIHC analysis of FSP1/AIFM2 using anti-FSP1/AIFM2 antibody (A06541-2). FSP1/AIFM2 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FSP1/AIFM2 Antibody (A06541-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1238862026-03-13T05:05:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01721-1-piezo1-primary-antibodies-wb-testing-1.jpgAnti-Piezo1 (extracellular domain) AntibodyWestern blot analysis of Piezo1 using anti-Piezo1 antibody (A01721-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Piezo1 antigen affinity purified polyclonal antibody (A01721-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Piezo1 at approximately 300 kDa. The expected band size for Piezo1 is at 287 kDa. https://www.bosterbio.com/catalog/product/view/id/1238872026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238882026-03-16T05:08:11+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238892026-03-16T05:08:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05146-2-ndufv1-primary-antibodies-wb-testing-1.jpgAnti-NDUFV1 AntibodyWestern blot analysis of NDUFV1 using anti-NDUFV1 antibody (A05146-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: rat kidney tissue lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFV1 antigen affinity purified polyclonal antibody (A05146-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NDUFV1 at approximately 51 kDa. The expected band size for NDUFV1 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05146-2-ndufv1-primary-antibodies-ihc-testing-1.jpgAnti-NDUFV1 AntibodyIHC analysis of NDUFV1 using anti-NDUFV1 antibody (A05146-2). NDUFV1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-NDUFV1 Antibody (A05146-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1238902026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-wb-testing-1.jpgAnti-NUSAP1 Antibody Picoband® Western blot analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUSAP1 antigen affinity purified polyclonal antibody (A06066-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NUSAP1 at approximately 52 kDa. The expected band size for NUSAP1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-ihc-testing-2.jpgAnti-NUSAP1 Antibody Picoband® IHC analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). NUSAP1 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NUSAP1 Antibody (A06066-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-ihc-testing-3.jpgAnti-NUSAP1 Antibody Picoband® IHC analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). NUSAP1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NUSAP1 Antibody (A06066-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-ihc-testing-4.jpgAnti-NUSAP1 Antibody Picoband® IHC analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). NUSAP1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NUSAP1 Antibody (A06066-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-ihc-testing-5.jpgAnti-NUSAP1 Antibody Picoband® IHC analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). NUSAP1 was detected in a paraffin-embedded section of mouse epididymis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NUSAP1 Antibody (A06066-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-ihc-testing-6.jpgAnti-NUSAP1 Antibody Picoband® IHC analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). NUSAP1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-NUSAP1 Antibody (A06066-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-wb-testing-1_1.jpgAnti-NUSAP1 Antibody Picoband®Western blot analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUSAP1 antigen affinity purified polyclonal antibody (A06066-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NUSAP1 at approximately 60 kDa. The expected band size for NUSAP1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-ihc-testing-1.jpgAnti-NUSAP1 Antibody Picoband®IHC analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). NUSAP1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUSAP1 Antibody (A06066-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-if-testing-1.jpgAnti-NUSAP1 Antibody Picoband®IF analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2). NUSAP1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NUSAP1 Antibody (A06066-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-if-testing-2.jpgAnti-NUSAP1 Antibody Picoband®IF analysis of NUSAP1 using anti-NUSAP1 antibody (A06066-2) and anti-Beta Tubulin antibody (M01857-3). NUSAP1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUSAP1 Antibody (A06066-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06066-2-nusap1-primary-antibodies-fcm-testing-1.jpgAnti-NUSAP1 Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-NUSAP1 antibody (A06066-2). Overlay histogram showing U251 cells stained with A06066-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUSAP1 Antibody (A06066-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1238912026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06773-1-plod3-primary-antibodies-ihc-testing-1.jpgAnti-PLOD3 AntibodyIHC analysis of PLOD3 using anti-PLOD3 antibody (A06773-1). PLOD3 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-PLOD3 Antibody (A06773-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06773-1-plod3-primary-antibodies-wb-testing-1.jpgAnti-PLOD3 AntibodyWestern blot analysis of PLOD3 using anti-PLOD3 antibody (A06773-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLOD3 antigen affinity purified polyclonal antibody (A06773-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PLOD3 at approximately 85 kDa. The expected band size for PLOD3 is at 85 kDa. https://www.bosterbio.com/catalog/product/view/id/1238922026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02904-2-s1pr2-primary-antibodies-wb-testing-1_1.jpgAnti-S1PR2 AntibodyWestern blot analysis of S1PR2 using anti-S1PR2 antibody (A02904-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HUH-7 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human MDA-MB-231 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-S1PR2 antigen affinity purified polyclonal antibody (A02904-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for S1PR2 at approximately 45 kDa. The expected band size for S1PR2 is at 39 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-scd-picoband-trade-antibody-a00588-1-boster.html2026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-1-scd-primary-antibodies-wb-testing-1.jpgAnti-SCD Antibody Picoband® Western blot analysis of SCD using anti-SCD antibody (A00588-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCD antigen affinity purified polyclonal antibody (Catalog # A00588-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SCD at approximately 37,42 kDa. The expected band size for SCD is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-1-scd-primary-antibodies-ihc-testing-2.jpgAnti-SCD Antibody Picoband® IHC analysis of SCD using anti-SCD antibody (A00588-1). SCD was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCD Antibody (A00588-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-1-scd-primary-antibodies-ihc-testing-3.jpgAnti-SCD Antibody Picoband® IHC analysis of SCD using anti-SCD antibody (A00588-1). SCD was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCD Antibody (A00588-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-1-scd-primary-antibodies-ihc-testing-4.jpgAnti-SCD Antibody Picoband® IHC analysis of SCD using anti-SCD antibody (A00588-1). SCD was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCD Antibody (A00588-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-1-scd-primary-antibodies-fcm-testing-5.pngAnti-SCD Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-SCD antibody (A00588-1). Overlay histogram showing A549 cells stained with A00588-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SCD Antibody (A00588-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1238942026-04-03T05:00:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06085-1-stx17-primary-antibodies-wb-testing-1.jpgAnti-STX17 Antibody Picoband®Western blot analysis of STX17 using anti-STX17 antibody (A06085-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STX17 antigen affinity purified polyclonal antibody (A06085-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STX17 at approximately 37 kDa. The expected band size for STX17 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06085-1-stx17-primary-antibodies-ihc-testing-1.jpgAnti-STX17 Antibody Picoband®IHC analysis of STX17 using anti-STX17 antibody (A06085-1). STX17 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STX17 Antibody (A06085-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06085-1-stx17-primary-antibodies-ihc-testing-2.jpgAnti-STX17 Antibody Picoband®IHC analysis of STX17 using anti-STX17 antibody (A06085-1). STX17 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STX17 Antibody (A06085-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06085-1-stx17-primary-antibodies-if-testing-1.jpgAnti-STX17 Antibody Picoband®IF analysis of STX17 using anti-STX17 antibody (A06085-1). STX17 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-STX17 Antibody (A06085-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06085-1-stx17-primary-antibodies-ip-testing-1.jpgAnti-STX17 Antibody Picoband®Immunoprecipitating STX17 in Jurkat whole cell lysate. Western blot analysis of STX17 using anti-STX17 antibody (A06085-1). Lane 1: Jurkat whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-STX17 antibody in Jurkat whole cell lysate, Lane 3: anti-STX17 antibody (2μg) + Jurkat whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-STX17 antigen affinity purified polyclonal antibody (A06085-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for STX17 at approximately 37 kDa. The expected band size for STX17 is at 33 kDa. https://www.bosterbio.com/catalog/product/view/id/1238952026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238962026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06266-1-chchd2-primary-antibodies-wb-testing-1.jpgAnti-CHCHD2 AntibodyWestern blot analysis of CHCHD2 using anti-CHCHD2 antibody (A06266-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HT1080 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHCHD2 antigen affinity purified polyclonal antibody (A06266-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHCHD2 at approximately 18 kDa. The expected band size for CHCHD2 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06266-1-chchd2-primary-antibodies-ihc-testing-1.jpgAnti-CHCHD2 AntibodyIHC analysis of CHCHD2 using anti-CHCHD2 antibody (A06266-1). CHCHD2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CHCHD2 Antibody (A06266-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1238972026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02058-2-ent1-slc29a1-primary-antibodies-wb-testing-1.jpgAnti-ENT1/SLC29A1 Antibody Western blot analysis of ENT1/SLC29A1 using anti-ENT1/SLC29A1 antibody (A02058-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ENT1/SLC29A1 antigen affinity purified polyclonal antibody (A02058-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ENT1/SLC29A1 at approximately 75 kDa. The expected band size for ENT1/SLC29A1 is at 50 kDa. https://www.bosterbio.com/catalog/product/view/id/1238982026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1238992026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239002026-03-13T05:05:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02422-2-smmhc-myh11-primary-antibodies-wb-testing-1.jpgAnti-SMMHC/MYH11 Antibody Western blot analysis of SMMHC/MYH11 using anti-SMMHC/MYH11 antibody (A02422-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat small intestine tissue lysates, Lane 2: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMMHC/MYH11 antigen affinity purified polyclonal antibody (A02422-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SMMHC/MYH11 at approximately 250 kDa. The expected band size for SMMHC/MYH11 is at 228 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02422-2-smmhc-myh11-primary-antibodies-ihc-testing-2.jpgAnti-SMMHC/MYH11 Antibody IHC analysis of SMMHC/MYH11 using anti-SMMHC/MYH11 antibody (A02422-2). SMMHC/MYH11 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-SMMHC/MYH11 Antibody (A02422-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02422-2-smmhc-myh11-primary-antibodies-ihc-testing-3.jpgAnti-SMMHC/MYH11 Antibody IHC analysis of SMMHC/MYH11 using anti-SMMHC/MYH11 antibody (A02422-2). SMMHC/MYH11 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-SMMHC/MYH11 Antibody (A02422-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239012026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04863-1-1-lpcat1-primary-antibodies-wb-testing-1.jpgAnti-LPCAT1 AntibodyWestern blot analysis of LPCAT1 using anti-LPCAT1 antibody (A04863-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LPCAT1 antigen affinity purified polyclonal antibody (A04863-1) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LPCAT1 at approximately 59 kDa. The expected band size for LPCAT1 is at 59 kDa. https://www.bosterbio.com/catalog/product/view/id/1239022026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239032026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239042026-03-13T05:05:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02977-1-tip47-plin3-primary-antibodies-wb-testing-1.jpgAnti-TIP47/PLIN3 Antibody Western blot analysis of TIP47/PLIN3 using anti-TIP47/PLIN3 antibody (A02977-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIP47/PLIN3 antigen affinity purified polyclonal antibody (A02977-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TIP47/PLIN3 at approximately 47 kDa. The expected band size for TIP47/PLIN3 is at 47 kDa. https://www.bosterbio.com/catalog/product/view/id/1239052026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-wb-testing-1.jpgAnti-CAMKK2 Antibody Picoband® Western blot analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAMKK2 antigen affinity purified polyclonal antibody (A03048) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CAMKK2 at approximately 65 kDa. The expected band size for CAMKK2 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-ihc-testing-2.jpgAnti-CAMKK2 Antibody Picoband® IHC analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-ihc-testing-3.jpgAnti-CAMKK2 Antibody Picoband® IHC analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-ihc-testing-4.jpgAnti-CAMKK2 Antibody Picoband® IHC analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-ihc-testing-5.jpgAnti-CAMKK2 Antibody Picoband® IHC analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-ihc-testing-6.jpgAnti-CAMKK2 Antibody Picoband® IHC analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-if-testing-7.jpgAnti-CAMKK2 Antibody Picoband® IF analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. Cy3-conjugated Anti-rabbit IgG Secondary Antibody (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-if-testing-8.jpgAnti-CAMKK2 Antibody Picoband® IF analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03048-camkk2-primary-antibodies-if-testing-9.jpgAnti-CAMKK2 Antibody Picoband® IF analysis of CAMKK2 using anti-CAMKK2 antibody (A03048). CAMKK2 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/ml rabbit anti-CAMKK2 Antibody (A03048) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239062026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-wb-testing-1.jpgAnti-UQCRC1 Antibody Western blot analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UQCRC1 antigen affinity purified polyclonal antibody (A06974-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UQCRC1 at approximately 45 kDa. The expected band size for UQCRC1 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-2.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of human colonic adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-3.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-4.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-5.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-6.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-7.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of human renal clear cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-8.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-9.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-10.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-ihc-testing-11.jpgAnti-UQCRC1 Antibody IHC analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in a paraffin-embedded section of mouse hippocampus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06974-1-uqcrc1-primary-antibodies-if-testing-1.jpgAnti-UQCRC1 AntibodyIF analysis of UQCRC1 using anti-UQCRC1 antibody (A06974-1). UQCRC1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-UQCRC1 Antibody (A06974-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239072026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239082026-04-03T05:00:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01865-1-trib3-primary-antibodies-wb-testing-1.jpgAnti-TRIB3 Antibody Picoband®Western blot analysis of TRIB3 using anti-TRIB3 antibody (A01865-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIB3 antigen affinity purified polyclonal antibody (A01865-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIB3 at approximately 40-45 kDa. The expected band size for TRIB3 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01414-2-trib3-primary-antibodies-wb-testing-1.jpgAnti-TRIB3 Antibody Picoband®Western blot analysis of TRIB3 using anti-TRIB3 antibody (A01414-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIB3 antigen affinity purified polyclonal antibody (A01414-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIB3 at approximately 40-45 kDa. The expected band size for TRIB3 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01414-2-trib3-primary-antibodies-fcm-testing-1.jpgAnti-TRIB3 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-TRIB3 antibody (A01414-2). Overlay histogram showing HepG2 cells stained with A01414-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TRIB3 Antibody (A01414-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239092026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06710-ttl-primary-antibodies-wb-testing-1.jpgAnti-TTL Antibody Picoband®Western blot analysis of TTL using anti-TTL antibody (A06710). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TTL antigen affinity purified polyclonal antibody (A06710) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TTL at approximately 43 kDa. The expected band size for TTL is at 43 kDa. https://www.bosterbio.com/catalog/product/view/id/1239102026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239112026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239122026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05867-2-ndufs3-primary-antibodies-wb-testing-1.jpgAnti-NDUFS3 Antibody Picoband® Western blot analysis of NDUFS3 using anti-NDUFS3 antibody (A05867-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFS3 antigen affinity purified polyclonal antibody (A05867-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NDUFS3 at approximately 26 kDa. The expected band size for NDUFS3 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05867-2-ndufs3-primary-antibodies-ihc-testing-2.jpgAnti-NDUFS3 Antibody Picoband® IHC analysis of NDUFS3 using anti-NDUFS3 antibody (A05867-2). NDUFS3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFS3 Antibody (A05867-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05867-2-ndufs3-primary-antibodies-ihc-testing-3.jpgAnti-NDUFS3 Antibody Picoband® IHC analysis of NDUFS3 using anti-NDUFS3 antibody (A05867-2). NDUFS3 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFS3 Antibody (A05867-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05867-2-ndufs3-primary-antibodies-ihc-testing-4.jpgAnti-NDUFS3 Antibody Picoband® IHC analysis of NDUFS3 using anti-NDUFS3 antibody (A05867-2). NDUFS3 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFS3 Antibody (A05867-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05867-2-ndufs3-primary-antibodies-fcm-testing-5.jpgAnti-NDUFS3 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-NDUFS3 antibody (A05867-2). Overlay histogram showing CACO-2 cells stained with A05867-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NDUFS3 Antibody (A05867-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239132026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04236-1-ahcy-primary-antibodies-wb-testing-1.jpgAnti-AHCY Antibody Picoband® Western blot analysis of AHCY using anti-AHCY antibody (A04236-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat thymus tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AHCY antigen affinity purified polyclonal antibody (A04236-1) at 0.5 μg/ml overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for AHCY at approximately 45-48 kDa. The expected band size for AHCY is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04236-1-ahcy-primary-antibodies-ihc-testing-2.jpgAnti-AHCY Antibody Picoband® IHC analysis of AHCY using anti-AHCY antibody (A04236-1). AHCY was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHCY Antibody (A04236-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04236-1-ahcy-primary-antibodies-ihc-testing-3.jpgAnti-AHCY Antibody Picoband® IHC analysis of AHCY using anti-AHCY antibody (A04236-1). AHCY was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHCY Antibody (A04236-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239142026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239152026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-wb-testing-1.jpgAnti-CHCHD3 Antibody Picoband® Western blot analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat RH-35 whole cell lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHCHD3 antigen affinity purified polyclonal antibody (A06593-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHCHD3 at approximately 26 kDa. The expected band size for CHCHD3 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-ihc-testing-2.jpgAnti-CHCHD3 Antibody Picoband® IHC analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). CHCHD3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CHCHD3 Antibody (A06593-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-ihc-testing-3.jpgAnti-CHCHD3 Antibody Picoband® IHC analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). CHCHD3 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CHCHD3 Antibody (A06593-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-ihc-testing-4.jpgAnti-CHCHD3 Antibody Picoband® IHC analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). CHCHD3 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CHCHD3 Antibody (A06593-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-wb-testing-1_1.jpgAnti-CHCHD3 Antibody Picoband®Western blot analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHCHD3 antigen affinity purified polyclonal antibody (A06593-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHCHD3 at approximately 26 kDa. The expected band size for CHCHD3 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-ihc-testing-1.jpgAnti-CHCHD3 Antibody Picoband®IHC analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). CHCHD3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHCHD3 Antibody (A06593-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-ihc-testing-2_1.jpgAnti-CHCHD3 Antibody Picoband®IHC analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). CHCHD3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHCHD3 Antibody (A06593-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-if-testing-1.jpgAnti-CHCHD3 Antibody Picoband®IF analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2) and anti-Alpha Tubulin antibody (M03989-3). CHCHD3 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CHCHD3 Antibody (A06593-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-ip-testing-1.jpgAnti-CHCHD3 Antibody Picoband®Immunoprecipitating CHCHD3 in U251 whole cell lysate. Western blot analysis of CHCHD3 using anti-CHCHD3 antibody (A06593-2). Lane 1: U251 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-CHCHD3 antibody in U251 whole cell lysate, Lane 3: anti-CHCHD3 antibody (2μg) + U251 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CHCHD3 antigen affinity purified polyclonal antibody (A06593-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for CHCHD3 at approximately 26 kDa. The expected band size for CHCHD3 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06593-2-chchd3-primary-antibodies-fcm-testing-1.jpgAnti-CHCHD3 Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-CHCHD3 antibody (A06593-2). Overlay histogram showing SH-SY5Y cells stained with A06593-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHCHD3 Antibody (A06593-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239162026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239172026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239182026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239202026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-ent1-iscu-primary-antibodies-wb-testing-1.jpgAnti-ISCU Antibody Western blot analysis of ENT1/ISCU using anti-ENT1/ISCU antibody (A05447-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human COLO320 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ENT1/ISCU antigen affinity purified polyclonal antibody (A05447-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ENT1/ISCU at approximately 15 kDa. The expected band size for ENT1/ISCU is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-iscu-primary-antibodies-ihc-testing-6.jpgAnti-ISCU Antibody IHC analysis of ISCU using anti-ISCU antibody (A05447-1). ISCU was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ISCU Antibody (A05447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-iscu-primary-antibodies-ihc-testing-7.jpgAnti-ISCU Antibody IHC analysis of ISCU using anti-ISCU antibody (A05447-1). ISCU was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ISCU Antibody (A05447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-iscu-primary-antibodies-ihc-testing-5.jpgAnti-ISCU Antibody IHC analysis of ISCU using anti-ISCU antibody (A05447-1). ISCU was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ISCU Antibody (A05447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-iscu-primary-antibodies-ihc-testing-4.jpgAnti-ISCU Antibody IHC analysis of ISCU using anti-ISCU antibody (A05447-1). ISCU was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ISCU Antibody (A05447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-iscu-primary-antibodies-ihc-testing-3.jpgAnti-ISCU Antibody IHC analysis of ISCU using anti-ISCU antibody (A05447-1). ISCU was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ISCU Antibody (A05447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-iscu-primary-antibodies-ihc-testing-2.jpgAnti-ISCU Antibody IHC analysis of ISCU using anti-ISCU antibody (A05447-1). ISCU was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ISCU Antibody (A05447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05447-1-iscu-primary-antibodies-if-testing-1.jpgAnti-ISCU AntibodyIF analysis of ISCU using anti-ISCU antibody (A05447-1). ISCU was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated at 1:50 rabbit anti-ISCU Antibody (A05447-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239212026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239222026-04-02T05:00:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05802-1-dnajb11-primary-antibodies-wb-testing-1.jpgAnti-DNAJB11 Antibody Picoband®Western blot analysis of DNAJB11 using anti-DNAJB11 antibody (A05802-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJB11 antigen affinity purified polyclonal antibody (A05802-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNAJB11 at approximately 41 kDa. The expected band size for DNAJB11 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05802-1-dnajb11-primary-antibodies-ihc-testing-1.jpgAnti-DNAJB11 Antibody Picoband®IHC analysis of DNAJB11 using anti-DNAJB11 antibody (A05802-1). DNAJB11 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNAJB11 Antibody (A05802-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239242026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239252026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00135-1-eif4e-primary-antibodies-wb-testing-1.jpgAnti-EIF4E Antibody Picoband®Western blot analysis of EIF4E using anti-EIF4E antibody (A00135-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF4E antigen affinity purified polyclonal antibody (A00135-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EIF4E at approximately 25 kDa. The expected band size for EIF4E is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00135-1-eif4e-primary-antibodies-if-testing-1.jpgAnti-EIF4E Antibody Picoband®IF analysis of EIF4E using anti-EIF4E antibody (A00135-1). EIF4E was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-EIF4E Antibody (A00135-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00135-1-eif4e-primary-antibodies-fcm-testing-1.jpgAnti-EIF4E Antibody Picoband®Flow Cytometry analysis of K562 cells using anti-EIF4E antibody (A00135-1). Overlay histogram showing K562 cells stained with A00135-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EIF4E Antibody (A00135-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239262026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05901-2-ankrd2-primary-antibodies-wb-testing-1.jpgAnti-ANKRD2 Antibody Western blot analysis of ANKRD2 using anti-ANKRD2 antibody (A05901-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat skeletal muscle tissue lysates, Lane 5: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANKRD2 antigen affinity purified polyclonal antibody (A05901-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ANKRD2 at approximately 40 kDa. The expected band size for ANKRD2 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05901-2-ankrd2-primary-antibodies-ihc-testing-1.jpgAnti-ANKRD2 AntibodyIHC analysis of ANKRD2 using anti-ANKRD2 antibody (A05901-2). ANKRD2 was detected in a paraffin-embedded section of human heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ANKRD2 Antibody (A05901-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239272026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-1.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-2.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-3.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-4.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-5.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-6.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-7.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-8.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-9.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-10.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-ihc-testing-11.jpgAnti-ANP32B AntibodyIHC analysis of ANP32B using anti-ANP32B antibody (A05822-1). ANP32B was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ANP32B Antibody (A05822-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05822-1-anp32b-primary-antibodies-wb-testing-1.jpgAnti-ANP32B AntibodyWestern blot analysis of ANP32B using anti-ANP32B antibody (A05822-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANP32B antigen affinity purified polyclonal antibody (A05822-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ANP32B at approximately 29 kDa. The expected band size for ANP32B is at 29 kDa. https://www.bosterbio.com/catalog/product/view/id/1239282026-03-16T05:08:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06393-1-ant1-2-primary-antibodies-wb-testing-1.jpgAnti-ANT1/2 Antibody Western blot analysis of ANT1/2 using anti-ANT1/2 antibody (A06393-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANT1/2 antigen affinity purified polyclonal antibody (A06393-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ANT1/2 at approximately 33, 60 kDa. The expected band size for ANT1/2 is at 33 kDa. https://www.bosterbio.com/catalog/product/view/id/1239292026-03-16T05:08:12+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239302026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239312026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239322026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06614-1-fndc3b-primary-antibodies-wb-testing-1.jpgAnti-FNDC3B Antibody Picoband®Western blot analysis of FNDC3B using anti-FNDC3B antibody (A06614-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FNDC3B antigen affinity purified polyclonal antibody (A06614-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FNDC3B at approximately 160 kDa. The expected band size for FNDC3B is at 133 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06614-1-fndc3b-primary-antibodies-ip-testing-1.jpgAnti-FNDC3B Antibody Picoband®Immunoprecipitating FNDC3B in HepG2 whole cell lysate. Western blot analysis of FNDC3B using anti-FNDC3B antibody (A06614-1). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-FNDC3B antibody in HepG2 whole cell lysate, Lane 3: anti-FNDC3B antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FNDC3B antigen affinity purified polyclonal antibody (A06614-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for FNDC3B at approximately 160 kDa. The expected band size for FNDC3B is at 133 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06614-1-fndc3b-primary-antibodies-fcm-testing-1.jpgAnti-FNDC3B Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-FNDC3B antibody (A06614-1). Overlay histogram showing U251 cells stained with A06614-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-FNDC3B Antibody (A06614-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239332026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239342026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239352026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239362026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239372026-03-16T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13191-2-usp38-primary-antibodies-wb-testing-1.jpgAnti-USP38 AntibodyWestern blot analysis of USP38 using anti-USP38 antibody (A13191-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-USP38 antigen affinity purified polyclonal antibody (A13191-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for USP38 at approximately 117 kDa. The expected band size for USP38 is at 117 kDa. https://www.bosterbio.com/catalog/product/view/id/1239382026-03-16T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08911-1-vilip3-hpcal1-primary-antibodies-wb-testing-1.jpgAnti-VILIP3/HPCAL1 Antibody Western blot analysis of VILIP3/HPCAL1 using anti-VILIP3/HPCAL1 antibody (A08911-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VILIP3/HPCAL1 antigen affinity purified polyclonal antibody (A08911-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VILIP3/HPCAL1 at approximately 18 kDa. The expected band size for VILIP3/HPCAL1 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08911-1-vilip3-hpcal1-primary-antibodies-ihc-testing-2.jpgAnti-VILIP3/HPCAL1 Antibody IHC analysis of VILIP3/HPCAL1 using anti-VILIP3/HPCAL1 antibody (A08911-1). VILIP3/HPCAL1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VILIP3/HPCAL1 Antibody (A08911-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08911-1-vilip3-hpcal1-primary-antibodies-ihc-testing-3.jpgAnti-VILIP3/HPCAL1 Antibody IHC analysis of VILIP3/HPCAL1 using anti-VILIP3/HPCAL1 antibody (A08911-1). VILIP3/HPCAL1 was detected in a paraffin-embedded section of human renal clear cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VILIP3/HPCAL1 Antibody (A08911-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08911-1-vilip3-hpcal1-primary-antibodies-ihc-testing-4.jpgAnti-VILIP3/HPCAL1 Antibody IHC analysis of VILIP3/HPCAL1 using anti-VILIP3/HPCAL1 antibody (A08911-1). VILIP3/HPCAL1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VILIP3/HPCAL1 Antibody (A08911-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08911-1-vilip3-hpcal1-primary-antibodies-ihc-testing-5.jpgAnti-VILIP3/HPCAL1 Antibody IHC analysis of VILIP3/HPCAL1 using anti-VILIP3/HPCAL1 antibody (A08911-1). VILIP3/HPCAL1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VILIP3/HPCAL1 Antibody (A08911-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239392026-03-13T05:05:00+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239402026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239412026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239422026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239432026-03-16T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05723-1-aldh3b2-primary-antibodies-wb-testing-1.jpgAnti-ALDH3B2 AntibodyWestern blot analysis of ALDH3B2 using anti-ALDH3B2 antibody (A05723-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: rat lung tissue lysates, Lane 3: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALDH3B2 antigen affinity purified polyclonal antibody (A05723-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALDH3B2 at approximately 43 kDa. The expected band size for ALDH3B2 is at 43 kDa. https://www.bosterbio.com/catalog/product/view/id/1239442026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239452026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239462026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239472026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239492026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239502026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239512026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239522026-03-16T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05175-1-ribosomal-protein-l4-rpl4-primary-antibodies-wb-testing-1.jpgAnti-Ribosomal protein L4/RPL4 Antibody Western blot analysis of Ribosomal protein L4/RPL4 using anti-Ribosomal protein L4/RPL4 antibody (A05175-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse pancreas tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ribosomal protein L4/RPL4 antigen affinity purified polyclonal antibody (A05175-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Ribosomal protein L4/RPL4 at approximately 48 kDa. The expected band size for Ribosomal protein L4/RPL4 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05175-1-ribosomal-protein-l4-rpl4-primary-antibodies-ihc-testing-2.jpgAnti-Ribosomal protein L4/RPL4 Antibody IHC analysis of Ribosomal protein L4/RPL4 using anti-Ribosomal protein L4/RPL4 antibody (A05175-1). Ribosomal protein L4/RPL4 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Ribosomal protein L4/RPL4 Antibody (A05175-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05175-1-ribosomal-protein-l4-rpl4-primary-antibodies-ihc-testing-3.jpgAnti-Ribosomal protein L4/RPL4 Antibody IHC analysis of Ribosomal protein L4/RPL4 using anti-Ribosomal protein L4/RPL4 antibody (A05175-1). Ribosomal protein L4/RPL4 was detected in a paraffin-embedded section of mouse bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Ribosomal protein L4/RPL4 Antibody (A05175-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05175-1-ribosomal-protein-l4-rpl4-primary-antibodies-ihc-testing-4.jpgAnti-Ribosomal protein L4/RPL4 Antibody IHC analysis of Ribosomal protein L4/RPL4 using anti-Ribosomal protein L4/RPL4 antibody (A05175-1). Ribosomal protein L4/RPL4 was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Ribosomal protein L4/RPL4 Antibody (A05175-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05175-1-ribosomal-protein-l4-rpl4-primary-antibodies-if-testing-5.jpgAnti-Ribosomal protein L4/RPL4 Antibody IF analysis of Ribosomal protein L4/RPL4 using anti-Ribosomal protein L4/RPL4 antibody (A05175-1). Ribosomal protein L4/RPL4 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-Ribosomal protein L4/RPL4 Antibody (A05175-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239532026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04465-1-slc5a5-primary-antibodies-wb-testing-1.jpgAnti-SLC5A5 Antibody Western blot analysis of SLC5A5 using anti-SLC5A5 antibody (A04465-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC5A5 antigen affinity purified polyclonal antibody (A04465-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC5A5 at approximately 50 kDa. The expected band size for SLC5A5 is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04465-1-slc5a5-primary-antibodies-ihc-testing-2.jpgAnti-SLC5A5 Antibody IHC analysis of SLC5A5 using anti-SLC5A5 antibody (A04465-1). SLC5A5 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-SLC5A5 Antibody (A04465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04465-1-slc5a5-primary-antibodies-ihc-testing-3.jpgAnti-SLC5A5 Antibody IHC analysis of SLC5A5 using anti-SLC5A5 antibody (A04465-1). SLC5A5 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-SLC5A5 Antibody (A04465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04465-1-slc5a5-primary-antibodies-ihc-testing-4.jpgAnti-SLC5A5 AntibodyIHC analysis of SLC5A5 using anti-SLC5A5 antibody (A04465-1). SLC5A5 was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC5A5 Antibody (A04465-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239542026-03-13T05:05:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-wb-testing-1_1.jpgAnti-KLF5 Antibody Picoband®Western blot analysis of KLF5 using anti-KLF5 antibody (A00727-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human CACO-2 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KLF5 antigen affinity purified polyclonal antibody (A00727-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KLF5 at approximately 55 kDa. The expected band size for KLF5 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ihc-testing-1.jpgAnti-KLF5 Antibody Picoband®IHC analysis of KLF5 using anti-KLF5 antibody (A00727-1). KLF5 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KLF5 Antibody (A00727-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ihc-testing-2_1.jpgAnti-KLF5 Antibody Picoband®IHC analysis of KLF5 using anti-KLF5 antibody (A00727-1). KLF5 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KLF5 Antibody (A00727-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ihc-testing-3_1.jpgAnti-KLF5 Antibody Picoband®IHC analysis of KLF5 using anti-KLF5 antibody (A00727-1). KLF5 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KLF5 Antibody (A00727-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ihc-testing-4_1.jpgAnti-KLF5 Antibody Picoband®IHC analysis of KLF5 using anti-KLF5 antibody (A00727-1). KLF5 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KLF5 Antibody (A00727-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ihc-testing-5_1.jpgAnti-KLF5 Antibody Picoband®IHC analysis of KLF5 using anti-KLF5 antibody (A00727-1). KLF5 was detected in a paraffin-embedded section of rat pancrease tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KLF5 Antibody (A00727-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ihc-testing-6.jpgAnti-KLF5 Antibody Picoband®IHC analysis of KLF5 using anti-KLF5 antibody (A00727-1). KLF5 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KLF5 Antibody (A00727-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ihc-testing-7.jpgAnti-KLF5 Antibody Picoband®IHC analysis of KLF5 using anti-KLF5 antibody (A00727-1). KLF5 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-KLF5 Antibody (A00727-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-if-testing-1_1.jpgAnti-KLF5 Antibody Picoband®IF analysis of KLF5 using anti-KLF5 antibody (A00727-1) and anti-Alpha Tubulin antibody (M03989-3). KLF5 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-KLF5 Antibody (A00727-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-if-testing-2.jpgAnti-KLF5 Antibody Picoband®IF analysis of KLF5 using anti-KLF5 antibody (A00727-1) and anti-Alpha Tubulin antibody (M03989-3). KLF5 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-KLF5 Antibody (A00727-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and Fluoro488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00727-1-klf5-primary-antibodies-ip-testing-1.jpgAnti-KLF5 Antibody Picoband®Immunoprecipitating (IP) KLF5 in Hela whole cell lysate. Western blot analysis of KLF5 using anti-KLF5 antibody (A00727-1); Lane 1: Hela whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-KLF5 antibody in Hela whole cell lysate; Lane 3: anti-KLF5 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-KLF5 antigen affinity purified polyclonal antibody (A00727-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light Chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for KLF5 at approximately 55 kDa. The expected band size for KLF5 is at 51 kDa. https://www.bosterbio.com/catalog/product/view/id/1239552026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239562026-03-16T05:08:13+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239572026-03-16T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04199-1-zc3hav1-primary-antibodies-wb-testing-1.jpgAnti-ZC3HAV1 AntibodyWestern blot analysis of ZC3HAV1 using anti-ZC3HAV1 antibody (A04199-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ZC3HAV1 antigen affinity purified polyclonal antibody (A04199-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ZC3HAV1 at approximately 101 kDa. The expected band size for ZC3HAV1 is at 101 kDa. https://www.bosterbio.com/catalog/product/view/id/1239582026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03095-2-eif4a3-primary-antibodies-wb-testing-1.jpgAnti-EIF4A3 Antibody Picoband®Western blot analysis of EIF4A3 using anti-EIF4A3 antibody (A03095-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF4A3 antigen affinity purified polyclonal antibody (A03095-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EIF4A3 at approximately 47 kDa. The expected band size for EIF4A3 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03095-2-eif4a3-primary-antibodies-ihc-testing-1.jpgAnti-EIF4A3 Antibody Picoband®IHC analysis of EIF4A3 using anti-EIF4A3 antibody (A03095-2). EIF4A3 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF4A3 Antibody (A03095-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03095-2-eif4a3-primary-antibodies-ihc-testing-2.jpgAnti-EIF4A3 Antibody Picoband®IHC analysis of EIF4A3 using anti-EIF4A3 antibody (A03095-2). EIF4A3 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF4A3 Antibody (A03095-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03095-2-eif4a3-primary-antibodies-if-testing-1.jpgAnti-EIF4A3 Antibody Picoband®IF analysis of EIF4A3 using anti-EIF4A3 antibody (A03095-2) and anti-Beta Tubulin antibody (M01857-3). EIF4A3 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-EIF4A3 Antibody (A03095-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03095-2-eif4a3-primary-antibodies-ip-testing-1.jpgAnti-EIF4A3 Antibody Picoband®Immunoprecipitating EIF4A3 in 293T whole cell lysate. Western blot analysis of EIF4A3 using anti-EIF4A3 antibody (A03095-2). Lane 1: 293T whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-EIF4A3 antibody in 293T whole cell lysate, Lane 3: anti-EIF4A3 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-EIF4A3 antigen affinity purified polyclonal antibody (A03095-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for EIF4A3 at approximately 47 kDa. The expected band size for EIF4A3 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03095-2-eif4a3-primary-antibodies-fcm-testing-1.jpgAnti-EIF4A3 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-EIF4A3 antibody (A03095-2). Overlay histogram showing 293T cells stained with A03095-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EIF4A3 Antibody (A03095-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239592026-03-16T05:08:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-2-mrps35-primary-antibodies-wb-testing-1.jpgAnti-MRPS35 Antibody Western blot analysis of MRPS35 using anti-MRPS35 antibody (A13823-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MRPS35 antigen affinity purified polyclonal antibody (A13823-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MRPS35 at approximately 37 kDa. The expected band size for MRPS35 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-2-mrps35-primary-antibodies-ihc-testing-2.jpgAnti-MRPS35 Antibody IHC analysis of MRPS35 using anti-MRPS35 antibody (A13823-2). MRPS35 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MRPS35 Antibody (A13823-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-2-mrps35-primary-antibodies-ihc-testing-3.jpgAnti-MRPS35 Antibody IHC analysis of MRPS35 using anti-MRPS35 antibody (A13823-2). MRPS35 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MRPS35 Antibody (A13823-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13823-2-mrps35-primary-antibodies-if-testing-4.jpgAnti-MRPS35 Antibody IF analysis of MRPS35 using anti-MRPS35 antibody (A13823-2). MRPS35 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-MRPS35 Antibody (A13823-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239602026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239612026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239622026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05954-2-tmprss4-primary-antibodies-wb-testing-1.jpgAnti-TMPRSS4 Antibody Picoband®Western blot analysis of TMPRSS4 using anti-TMPRSS4 antibody (A05954-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: rat stomach tissue lysates, Lane 4: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TMPRSS4 antigen affinity purified polyclonal antibody (A05954-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TMPRSS4 at approximately 48 kDa. The expected band size for TMPRSS4 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05954-2-tmprss4-primary-antibodies-fcm-testing-1.jpgAnti-TMPRSS4 Antibody Picoband®Flow Cytometry analysis of RT4 cells using anti-TMPRSS4 antibody (A05954-2). Overlay histogram showing RT4 cells stained with A05954-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TMPRSS4 Antibody (A05954-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239632026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02861-2-ecm1-primary-antibodies-wb-testing-1.jpgAnti-ECM1 Antibody Picoband®Western blot analysis of ECM1 using anti-ECM1 antibody (A02861-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ECM1 antigen affinity purified polyclonal antibody (A02861-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ECM1 at approximately 61 kDa. The expected band size for ECM1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02861-2-ecm1-primary-antibodies-fcm-testing-1.jpgAnti-ECM1 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-ECM1 antibody (A02861-2). Overlay histogram showing HepG2 cells stained with A02861-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ECM1 Antibody (A02861-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239642026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239652026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01763-1-slc4a4-primary-antibodies-wb-testing-1.jpgAnti-SLC4A4 Antibody Picoband®Western blot analysis of SLC4A4 using anti-SLC4A4 antibody (A01763-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC4A4 antigen affinity purified polyclonal antibody (A01763-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC4A4 at approximately 121 kDa. The expected band size for SLC4A4 is at 121 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01763-1-slc4a4-primary-antibodies-ihc-testing-1.jpgAnti-SLC4A4 Antibody Picoband®IHC analysis of SLC4A4 using anti-SLC4A4 antibody (A01763-1). SLC4A4 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC4A4 Antibody (A01763-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01763-1-slc4a4-primary-antibodies-ihc-testing-2.jpgAnti-SLC4A4 Antibody Picoband®IHC analysis of SLC4A4 using anti-SLC4A4 antibody (A01763-1). SLC4A4 was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC4A4 Antibody (A01763-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01763-1-slc4a4-primary-antibodies-ihc-testing-3.jpgAnti-SLC4A4 Antibody Picoband®IHC analysis of SLC4A4 using anti-SLC4A4 antibody (A01763-1). SLC4A4 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC4A4 Antibody (A01763-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01763-1-slc4a4-primary-antibodies-ihc-testing-4.jpgAnti-SLC4A4 Antibody Picoband®IHC analysis of SLC4A4 using anti-SLC4A4 antibody (A01763-1). SLC4A4 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC4A4 Antibody (A01763-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01763-1-slc4a4-primary-antibodies-if-testing-1.jpgAnti-SLC4A4 Antibody Picoband®IF analysis of SLC4A4 using anti-SLC4A4 antibody (A01763-1). SLC4A4 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SLC4A4 Antibody (A01763-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01763-1-slc4a4-primary-antibodies-fcm-testing-1.jpgAnti-SLC4A4 Antibody Picoband®Flow Cytometry analysis of PC-3 cells using anti-SLC4A4 antibody (A01763-1). Overlay histogram showing PC-3 cells stained with A01763-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC4A4 Antibody (A01763-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239662026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239672026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239682026-03-13T05:05:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01583-4-gdf15-primary-antibodies-wb-testing-1.jpgAnti-GDF15 AntibodyWestern blot analysis of GDF15 using anti-GDF15 antibody (A01583-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HT1080 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GDF15 antigen affinity purified polyclonal antibody (A01583-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GDF15 at approximately 34 kDa. The expected band size for GDF15 is at 34 kDa. https://www.bosterbio.com/catalog/product/view/id/1239692026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239702026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239712026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239722026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239732026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239742026-03-17T05:15:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00215-3-alpha-synuclein-snca-primary-antibodies-wb-testing-1_1.jpgAnti-Alpha Synuclein/SNCA Antibody Picoband® Western blot analysis of Alpha Synuclein/SNCA using anti-Alpha Synuclein/SNCA antibody (A00215-3). Electrophoresis was performed on a 13% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha Synuclein/SNCA antigen affinity purified polyclonal antibody (A00215-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Alpha Synuclein/SNCA at approximately 18 kDa. The expected band size for Alpha Synuclein/SNCA is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00215-3-alpha-synuclein-snca-primary-antibodies-ihc-testing-2_1.jpgAnti-Alpha Synuclein/SNCA Antibody Picoband® IHC analysis of Alpha Synuclein/SNCA using anti-Alpha Synuclein/SNCA antibody (A00215-3). Alpha Synuclein/SNCA was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Alpha Synuclein/SNCA Antibody (A00215-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00215-3-alpha-synuclein-snca-primary-antibodies-ihc-testing-3_1.jpgAnti-Alpha Synuclein/SNCA Antibody Picoband® IHC analysis of Alpha Synuclein/SNCA using anti-Alpha Synuclein/SNCA antibody (A00215-3). Alpha Synuclein/SNCA was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Alpha Synuclein/SNCA Antibody (A00215-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00215-3-alpha-synuclein-snca-primary-antibodies-ihc-testing-4_1.jpgAnti-Alpha Synuclein/SNCA Antibody Picoband® IHC analysis of Alpha Synuclein/SNCA using anti-Alpha Synuclein/SNCA antibody (A00215-3). Alpha Synuclein/SNCA was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Alpha Synuclein/SNCA Antibody (A00215-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00215-3-snca-primary-antibodies-ihc-testing-5.jpgAnti-Alpha Synuclein/SNCA Antibody Picoband® IHC analysis of Alpha Synuclein/SNCA using anti-Alpha Synuclein/SNCA antibody (A00215-3). Alpha Synuclein/SNCA was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Alpha Synuclein/SNCA Antibody (A00215-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00215-3-alpha-synuclein-snca-primary-antibodies-if-testing-5.jpgAnti-Alpha Synuclein/SNCA Antibody Picoband® IF analysis of Alpha Synuclein/SNCA using anti-Alpha Synuclein/SNCA antibody (A00215-3). Alpha Synuclein/SNCA was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Alpha Synuclein/SNCA Antibody (A00215-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00215-3-alpha-synuclein-snca-primary-antibodies-fcm-testing-6.jpgAnti-Alpha Synuclein/SNCA Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-Alpha Synuclein/SNCA antibody (A00215-3). Overlay histogram showing U87 cells stained with A00215-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Alpha Synuclein/SNCA Antibody (A00215-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239752026-03-13T05:05:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03737-2-cytb-primary-antibodies-wb-testing-1.jpgAnti-CYTB/MT-CYB AntibodyWestern blot analysis of CYTB using anti-CYTB antibody (A03737-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MDA-MB-231 whole cell lysates, Lane 3: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYTB antigen affinity purified polyclonal antibody (A03737-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CYTB at approximately 43 kDa. The expected band size for CYTB is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03737-2-cytb-primary-antibodies-ihc-testing-1.jpgAnti-CYTB/MT-CYB AntibodyIHC analysis of CYTB using anti-CYTB antibody (A03737-2). CYTB was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CYTB Antibody (A03737-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03737-2-cytb-primary-antibodies-ihc-testing-2.jpgAnti-CYTB/MT-CYB AntibodyIHC analysis of CYTB using anti-CYTB antibody (A03737-2). CYTB was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CYTB Antibody (A03737-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239762026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239772026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239782026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239792026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01218-1-tgfbi-primary-antibodies-wb-testing-1_1_1.jpgAnti-BIGH3/TGFBI Antibody Picoband®Western blot analysis of BIGH3/TGFBI using anti-BIGH3/TGFBI antibody (A01218-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse kidney tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BIGH3/TGFBI antigen affinity purified polyclonal antibody (A01218-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for BIGH3/TGFBI at approximately 70 kDa. The expected band size for BIGH3/TGFBI is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01218-1-tgfbi-primary-antibodies-ihc-testing-1.jpgAnti-BIGH3/TGFBI Antibody Picoband®IHC analysis of BIGH3/TGFBI using anti-BIGH3/TGFBI antibody (A01218-1). BIGH3/TGFBI was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BIGH3/TGFBI Antibody (A01218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01218-1-tgfbi-primary-antibodies-ihc-testing-2.jpgAnti-BIGH3/TGFBI Antibody Picoband®IHC analysis of BIGH3/TGFBI using anti-BIGH3/TGFBI antibody (A01218-1). BIGH3/TGFBI was detected in a paraffin-embedded section of human intestinal smooth muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BIGH3/TGFBI Antibody (A01218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01218-1-tgfbi-primary-antibodies-if-testing-1.jpgAnti-BIGH3/TGFBI Antibody Picoband®IF analysis of BIGH3/TGFBI using anti-BIGH3/TGFBI antibody (A01218-1). BIGH3/TGFBI was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BIGH3/TGFBI Antibody (A01218-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01218-1-tgfbi-primary-antibodies-fcm-testing-1.jpgAnti-BIGH3/TGFBI Antibody Picoband®Flow Cytometry analysis of Hela cells using anti-BIGH3/TGFBI antibody (A01218-1). Overlay histogram showing Hela cells stained with A01218-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-BIGH3/TGFBI Antibody (A01218-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239802026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-wb-testing-1.jpgAnti-SHMT2 Antibody Picoband® Western blot analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates, Lane 7: mouse ANA-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHMT2 antigen affinity purified polyclonal antibody (A03233-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SHMT2 at approximately 56 kDa. The expected band size for SHMT2 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-wb-testing-1_1.jpgAnti-SHMT2 Antibody Picoband®Western blot analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHMT2 antigen affinity purified polyclonal antibody (A03233-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SHMT2 at approximately 56 kDa. The expected band size for SHMT2 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-1.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-2.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-3.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-4.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-5.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-6.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-7.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-8.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-9.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-10.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-11.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-12.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-if-testing-1.jpgAnti-SHMT2 Antibody Picoband®IF analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-if-testing-2.jpgAnti-SHMT2 Antibody Picoband®IF analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-if-testing-3.jpgAnti-SHMT2 Antibody Picoband®IF analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ip-testing-1.jpgAnti-SHMT2 Antibody Picoband®Immunoprecipitating SHMT2 in 293T whole cell lysate. Western blot analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). Lane 1: 293T whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-SHMT2 antibody in 293T whole cell lysate, Lane 3: anti-SHMT2 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SHMT2 antigen affinity purified polyclonal antibody (A03233-1) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for SHMT2 at approximately 56 kDa. The expected band size for SHMT2 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-fcm-testing-1.jpgAnti-SHMT2 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-SHMT2 antibody (A03233-1). Overlay histogram showing HepG2 cells stained with A03233-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SHMT2 Antibody (A03233-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-13.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03233-1-shmt2-primary-antibodies-ihc-testing-14.jpgAnti-SHMT2 Antibody Picoband®IHC analysis of SHMT2 using anti-SHMT2 antibody (A03233-1). SHMT2 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHMT2 Antibody (A03233-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239812026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04108-1-stoml2-primary-antibodies-wb-testing-1.jpgAnti-STOML2 Antibody Picoband®Western blot analysis of STOML2 using anti-STOML2 antibody (A04108-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STOML2 antigen affinity purified polyclonal antibody (A04108-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STOML2 at approximately 39 kDa. The expected band size for STOML2 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04108-1-stoml2-primary-antibodies-ihc-testing-1.jpgAnti-STOML2 Antibody Picoband®IHC analysis of STOML2 using anti-STOML2 antibody (A04108-1). STOML2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STOML2 Antibody (A04108-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04108-1-stoml2-primary-antibodies-ip-testing-1.jpgAnti-STOML2 Antibody Picoband®Immunoprecipitating STOML2 in jurkat whole cell lysate. Western blot analysis of STOML2 using anti-STOML2 antibody (A04108-1). Lane 1: jurkat whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-STOML2 antibody in jurkat whole cell lysate, Lane 3: anti-STOML2 antibody (2μg) + jurkat whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-STOML2 antigen affinity purified polyclonal antibody (A04108-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for STOML2 at approximately 39 kDa. The expected band size for STOML2 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04108-1-stoml2-primary-antibodies-fcm-testing-1.jpgAnti-STOML2 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-STOML2 antibody (A04108-1). Overlay histogram showing Jurkat cells stained with A04108-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-STOML2 Antibody (A04108-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239822026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239832026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239842026-04-02T05:00:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02141-2-eef1a1-primary-antibodies-wb-testing-1.jpgAnti-EEF1A1 Antibody Picoband®Western blot analysis of EEF1A1 using anti-EEF1A1 antibody (A02141-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: rat NRK whole cell lysates, Lane 4: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EEF1A1 antigen affinity purified polyclonal antibody (A02141-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EEF1A1 at approximately 50 kDa. The expected band size for EEF1A1 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02141-2-eef1a1-primary-antibodies-if-testing-1.jpgAnti-EEF1A1 Antibody Picoband®IF analysis of EEF1A1 using anti-EEF1A1 antibody (A02141-2). EEF1A1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-EEF1A1 Antibody (A02141-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239852026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239862026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239872026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239882026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239892026-04-02T05:00:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07179-1-chchd4-primary-antibodies-wb-testing-1.jpgAnti-CHCHD4 Antibody Picoband®Western blot analysis of CHCHD4 using anti-CHCHD4 antibody (A07179-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Daudi whole cell lysates, Lane 2: human Ramos whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHCHD4 antigen affinity purified polyclonal antibody (A07179-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHCHD4 at approximately 22 kDa. The expected band size for CHCHD4 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07179-1-chchd4-primary-antibodies-ihc-testing-1.jpgAnti-CHCHD4 Antibody Picoband®IHC analysis of CHCHD4 using anti-CHCHD4 antibody (A07179-1). CHCHD4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHCHD4 Antibody (A07179-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07179-1-chchd4-primary-antibodies-if-testing-1.jpgAnti-CHCHD4 Antibody Picoband®IF analysis of CHCHD4 using anti-CHCHD4 antibody (A07179-1). CHCHD4 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CHCHD4 Antibody (A07179-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239902026-03-16T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05376-1-asgr1-primary-antibodies-wb-testing-1.jpgAnti-ASGR1 Antibody Western blot analysis of ASGR1 using anti-ASGR1 antibody (A05376-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ASGR1 antigen affinity purified polyclonal antibody (A05376-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ASGR1 at approximately 38 kDa. The expected band size for ASGR1 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05376-1-asgr1-primary-antibodies-ihc-testing-2.jpgAnti-ASGR1 Antibody IHC analysis of ASGR1 using anti-ASGR1 antibody (A05376-1). ASGR1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ASGR1 Antibody (A05376-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05376-1-asgr1-primary-antibodies-ihc-testing-3.jpgAnti-ASGR1 Antibody IHC analysis of ASGR1 using anti-ASGR1 antibody (A05376-1). ASGR1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ASGR1 Antibody (A05376-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05376-1-asgr1-primary-antibodies-ihc-testing-4.jpgAnti-ASGR1 Antibody IHC analysis of ASGR1 using anti-ASGR1 antibody (A05376-1). ASGR1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ASGR1 Antibody (A05376-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239912026-03-16T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05012-2-transgelin-2-tagln2-primary-antibodies-ihc-testing-1.jpgAnti-Transgelin 2/TAGLN2 Antibody IHC analysis of Transgelin 2/TAGLN2 using anti-Transgelin 2/TAGLN2 antibody (A05012-2). Transgelin 2/TAGLN2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Transgelin 2/TAGLN2 Antibody (A05012-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239922026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239932026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03054-1-acox1-primary-antibodies-wb-testing-1_1.jpgAnti-ACOX1 Antibody Picoband®Western blot analysis of ACOX1 using anti-ACOX1 antibody (A03054-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates, Lane 3: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACOX1 antigen affinity purified polyclonal antibody (A03054-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ACOX1 at approximately 22, 74 kDa. The expected band size for ACOX1 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03054-1-acox1-primary-antibodies-ihc-testing-1.jpgAnti-ACOX1 Antibody Picoband®IHC analysis of ACOX1 using anti-ACOX1 antibody (A03054-1). ACOX1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACOX1 Antibody (A03054-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03054-1-acox1-primary-antibodies-ihc-testing-2.jpgAnti-ACOX1 Antibody Picoband®IHC analysis of ACOX1 using anti-ACOX1 antibody (A03054-1). ACOX1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACOX1 Antibody (A03054-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03054-1-acox1-primary-antibodies-if-testing-1.jpgAnti-ACOX1 Antibody Picoband®IF analysis of ACOX1 using anti-ACOX1 antibody (A03054-1). ACOX1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ACOX1 Antibody (A03054-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1239942026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03259-2-slc2a3-primary-antibodies-wb-testing-1.jpgAnti-GLUT3/SLC2A3 Antibody Picoband®Western blot analysis of SLC2A3 using anti-SLC2A3 antibody (A03259-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse testis tissue lysates, Lane 2: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC2A3 antigen affinity purified polyclonal antibody (A03259-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC2A3 at approximately 54 kDa. The expected band size for SLC2A3 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03259-2-slc2a3-primary-antibodies-fcm-testing-1.jpgAnti-GLUT3/SLC2A3 Antibody Picoband®Flow Cytometry analysis of Neuro-2a cells using anti-SLC2A3 antibody (A03259-2). Overlay histogram showing Neuro-2a cells stained with A03259-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC2A3 Antibody (A03259-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1239952026-03-13T05:05:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02515-2-urat1-slc22a12-primary-antibodies-wb-testing-1.jpgAnti-URAT1/SLC22A12 AntibodyWestern blot analysis of URAT1/SLC22A12 using anti-URAT1/SLC22A12 antibody (A02515-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: mouse kidney tissue lysates, Lane 3: mouse Renca whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-URAT1/SLC22A12 antigen affinity purified polyclonal antibody (A02515-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for URAT1/SLC22A12 at approximately 60-70 kDa. The expected band size for URAT1/SLC22A12 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02515-2-urat1-slc22a12-primary-antibodies-ihc-testing-2.jpgAnti-URAT1/SLC22A12 Antibody IHC analysis of URAT1/SLC22A12 using anti-URAT1/SLC22A12 antibody (A02515-2). URAT1/SLC22A12 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-URAT1/SLC22A12 Antibody (A02515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02515-2-urat1-slc22a12-primary-antibodies-ihc-testing-3.jpgAnti-URAT1/SLC22A12 Antibody IHC analysis of URAT1/SLC22A12 using anti-URAT1/SLC22A12 antibody (A02515-2). URAT1/SLC22A12 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-URAT1/SLC22A12 Antibody (A02515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02515-2-urat1-slc22a12-primary-antibodies-ihc-testing-1.jpgAnti-URAT1/SLC22A12 Antibody IHC analysis of URAT1/SLC22A12 using anti-URAT1/SLC22A12 antibody (A02515-2). URAT1/SLC22A12 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-URAT1/SLC22A12 Antibody (A02515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239962026-03-13T05:05:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03994-2-jmjd1a-kdm3a-primary-antibodies-wb-testing-1.jpgAnti-JMJD1A/KDM3A Antibody Western blot analysis of JMJD1A/KDM3A using anti-JMJD1A/KDM3A antibody (A03994-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JMJD1A/KDM3A antigen affinity purified polyclonal antibody (A03994-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for JMJD1A/KDM3A at approximately 150 kDa. The expected band size for JMJD1A/KDM3A is at 147 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03994-2-kdm3a-primary-antibodies-ihc-testing-1.jpgAnti-JMJD1A/KDM3A AntibodyIHC analysis of JMJD1A/KDM3A using anti-JMJD1A/KDM3A antibody (A03994-2). JMJD1A/KDM3A was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-JMJD1A/KDM3A Antibody (A03994-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1239972026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-wb-testing-1.jpgAnti-PHGDH Antibody Picoband® Western blot analysis of PHGDH using anti-PHGDH antibody (A03355-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHGDH antigen affinity purified polyclonal antibody (A03355-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHGDH at approximately 57 kDa. The expected band size for PHGDH is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-ihc-testing-2.jpgAnti-PHGDH Antibody Picoband® IHC analysis of PHGDH using anti-PHGDH antibody (A03355-1). PHGDH was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHGDH Antibody (A03355-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-ihc-testing-1.jpgAnti-PHGDH Antibody Picoband®IHC analysis of PHGDH using anti-PHGDH antibody (A03355-1). PHGDH was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHGDH Antibody (A03355-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-ihc-testing-3.jpgAnti-PHGDH Antibody Picoband®IHC analysis of PHGDH using anti-PHGDH antibody (A03355-1). PHGDH was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHGDH Antibody (A03355-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-if-testing-3.jpgAnti-PHGDH Antibody Picoband® IF analysis of PHGDH using anti-PHGDH antibody (A03355-1). PHGDH was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PHGDH Antibody (A03355-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-if-testing-1.jpgAnti-PHGDH Antibody Picoband®IF analysis of PHGDH using anti-PHGDH antibody (A03355-1). PHGDH was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PHGDH Antibody (A03355-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-if-testing-2.jpgAnti-PHGDH Antibody Picoband®IF analysis of PHGDH using anti-PHGDH antibody (A03355-1). PHGDH was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PHGDH Antibody (A03355-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-fcm-testing-4.jpgAnti-PHGDH Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-PHGDH antibody (A03355-1). Overlay histogram showing PC-3 cells stained with A03355-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHGDH Antibody (A03355-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03355-1-phgdh-primary-antibodies-ip-testing-5.jpgAnti-PHGDH Antibody Picoband® Immunoprecipitating PHGDH in Jurkat whole cell lysate. Western blot analysis of PHGDH using anti-PHGDH antibody (A03355-1). Lane 1: Jurkat whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-PHGDH antibody in Jurkat whole cell lysate; Lane 3: anti-PHGDH antibody (2μg) + Jurkat whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PHGDH antigen affinity purified polyclonal antibody (A03355-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PHGDH at approximately 57 kDa. The expected band size for PHGDH is at 57 kDa. https://www.bosterbio.com/catalog/product/view/id/1239982026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1239992026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240002026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04007-1-slc39a8-primary-antibodies-wb-testing-1.jpgAnti-ZIP8/SLC39A8 Antibody Picoband®Western blot analysis of ZIP8/SLC39A8 using anti-ZIP8/SLC39A8 antibody (A04007-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: rat lung tissue lysates, Lane 3: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ZIP8/SLC39A8 antigen affinity purified polyclonal antibody (A04007-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ZIP8/SLC39A8 at approximately 80 kDa. The expected band size for ZIP8/SLC39A8 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04007-1-slc39a8-primary-antibodies-ihc-testing-1.jpgAnti-ZIP8/SLC39A8 Antibody Picoband®IHC analysis of ZIP8/SLC39A8 using anti-ZIP8/SLC39A8 antibody (A04007-1). ZIP8/SLC39A8 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ZIP8/SLC39A8 Antibody (A04007-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04007-1-slc39a8-primary-antibodies-fcm-testing-1.jpgAnti-ZIP8/SLC39A8 Antibody Picoband®Flow Cytometry analysis of HEL cells using anti-ZIP8/SLC39A8 antibody (A04007-1). Overlay histogram showing HEL cells stained with A04007-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ZIP8/SLC39A8 Antibody (A04007-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/https-www-bosterbio-com-anti-ctrc-picoband-antibody-a01866-3-boster-html.html2026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-wb-testing-1.jpgAnti-GLUD1 Antibody Picoband® Western blot analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human PC-3 whole cell lysates. Lane 5: rat liver tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLUD1 antigen affinity purified polyclonal antibody (A01866-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GLUD1 at approximately 55 kDa. The expected band size for GLUD1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-2.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human adrenal adenoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-3.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-4.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-5.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-6.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human osteosarcoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-7.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-8.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-9.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-ihc-testing-10.jpgAnti-GLUD1 Antibody Picoband® IHC analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-if-testing-11.jpgAnti-GLUD1 Antibody Picoband® IF analysis of GLUD1 using anti-GLUD1 antibody (A01866-3). GLUD1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 4 μg/mL rabbit anti-GLUD1 Antibody (A01866-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01866-3-glud1-primary-antibodies-fcm-testing-12.jpgAnti-GLUD1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GLUD1 antibody (A01866-3). Overlay histogram showing HepG2 cells stained with A04887-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLUD1 Antibody (A01866-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240022026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01800-1-pnpla2-primary-antibodies-wb-testing-1.jpgAnti-PNPLA2 Antibody Picoband®Western blot analysis of PNPLA2 using anti-PNPLA2 antibody (A01800-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PNPLA2 antigen affinity purified polyclonal antibody (A01800-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PNPLA2 at approximately 50 kDa. The expected band size for PNPLA2 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01800-1-pnpla2-primary-antibodies-ihc-testing-1.jpgAnti-PNPLA2 Antibody Picoband®IHC analysis of PNPLA2 using anti-PNPLA2 antibody (A01800-1). PNPLA2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PNPLA2 Antibody (A01800-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01800-1-pnpla2-primary-antibodies-ihc-testing-2.jpgAnti-PNPLA2 Antibody Picoband®IHC analysis of PNPLA2 using anti-PNPLA2 antibody (A01800-1). PNPLA2 was detected in a paraffin-embedded section of mouse adipose tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PNPLA2 Antibody (A01800-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01800-1-pnpla2-primary-antibodies-fcm-testing-1.jpgAnti-PNPLA2 Antibody Picoband®Flow Cytometry analysis of A431 cells using anti-PNPLA2 antibody (A01800-1). Overlay histogram showing A431 cells stained with A01800-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PNPLA2 Antibody (A01800-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240032026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09350-1-tctn1-primary-antibodies-wb-testing-1.jpgAnti-TCTN1 Antibody Picoband®Western blot analysis of TCTN1 using anti-TCTN1 antibody (A09350-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat thymus tissue lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TCTN1 antigen affinity purified polyclonal antibody (A09350-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TCTN1 at approximately 55 kDa. The expected band size for TCTN1 is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09350-1-tctn1-primary-antibodies-ihc-testing-1.jpgAnti-TCTN1 Antibody Picoband®IHC analysis of TCTN1 using anti-TCTN1 antibody (A09350-1). TCTN1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TCTN1 Antibody (A09350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09350-1-tctn1-primary-antibodies-ihc-testing-2.jpgAnti-TCTN1 Antibody Picoband®IHC analysis of TCTN1 using anti-TCTN1 antibody (A09350-1). TCTN1 was detected in a paraffin-embedded section of human fallopian tube tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TCTN1 Antibody (A09350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09350-1-tctn1-primary-antibodies-fcm-testing-1.jpgAnti-TCTN1 Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-TCTN1 antibody (A09350-1). Overlay histogram showing U251 cells stained with A09350-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TCTN1 Antibody (A09350-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240042026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240052026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240062026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02154-2-ckap4-primary-antibodies-wb-testing-1.jpgAnti-CKAP4 Antibody Picoband®Western blot analysis of CKAP4 using anti-CKAP4 antibody (A02154-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse NIH/3T3 whole cell lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CKAP4 antigen affinity purified polyclonal antibody (A02154-2) at 1:10000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CKAP4 at approximately 70 kDa. The expected band size for CKAP4 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02154-2-ckap4-primary-antibodies-wb-testing-1_1.jpgAnti-CKAP4 Antibody Picoband®Western blot analysis of CKAP4 using anti-CKAP4 antibody (A02154-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat H9C2(2-1) whole cell lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CKAP4 antigen affinity purified polyclonal antibody (A02154-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CKAP4 at approximately 66 kDa. The expected band size for CKAP4 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02154-2-ckap4-primary-antibodies-ihc-testing-1.jpgAnti-CKAP4 Antibody Picoband®IHC analysis of CKAP4 using anti-CKAP4 antibody (A02154-2). CKAP4 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CKAP4 Antibody (A02154-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02154-2-ckap4-primary-antibodies-ihc-testing-2.jpgAnti-CKAP4 Antibody Picoband®IHC analysis of CKAP4 using anti-CKAP4 antibody (A02154-2). CKAP4 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CKAP4 Antibody (A02154-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02154-2-ckap4-primary-antibodies-if-testing-1.jpgAnti-CKAP4 Antibody Picoband®IF analysis of CKAP4 using anti-CKAP4 antibody (A02154-2). CKAP4 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CKAP4 Antibody (A02154-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02154-2-ckap4-primary-antibodies-ip-testing-1.jpgAnti-CKAP4 Antibody Picoband®Immunoprecipitating CKAP4 in Hacat whole cell lysate. Western blot analysis of CKAP4 using anti-CKAP4 antibody (A02154-2). Lane 1: Hacat whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-CKAP4 antibody in Hacat whole cell lysate, Lane 3: anti-CKAP4 antibody (2μg) + Hacat whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CKAP4 antigen affinity purified polyclonal antibody (A02154-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for CKAP4 at approximately 66 kDa. The expected band size for CKAP4 is at 66 kDa. https://www.bosterbio.com/catalog/product/view/id/1240072026-03-16T05:08:14+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240082026-03-13T05:05:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01352-1-1-lats2-primary-antibodies-wb-testing-1.jpgAnti-LATS2 AntibodyWestern blot analysis of LATS2 using anti-LATS2 antibody (A01352-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human SIHA whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LATS2 antigen affinity purified polyclonal antibody (A01352-1) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LATS2 at approximately 150 kDa. The expected band size for LATS2 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01352-1-1-lats2-primary-antibodies-ihc-testing-1.jpgAnti-LATS2 AntibodyIHC analysis of LATS2 using anti-LATS2 antibody (A01352-1). LATS2 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 200 rabbit anti-LATS2 Antibody (A01352-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01352-1-1-lats2-primary-antibodies-ihc-testing-2.jpgAnti-LATS2 AntibodyIHC analysis of LATS2 using anti-LATS2 antibody (A01352-1). LATS2 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 200 rabbit anti-LATS2 Antibody (A01352-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240092026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-3-lrg1-primary-antibodies-wb-testing-1.jpgAnti-LRG1 Antibody Picoband® Western blot analysis of LRG1 using anti-LRG1 antibody (A04365-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat small intestine tissue lysates, Lane 4: rat RH-35 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRG1 antigen affinity purified polyclonal antibody (A04365-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LRG1 at approximately 38 kDa. The expected band size for LRG1 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-3-lrg1-primary-antibodies-ihc-testing-2.jpgAnti-LRG1 Antibody Picoband® IHC analysis of LRG1 using anti-LRG1 antibody (A04365-3). LRG1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LRG1 Antibody (A04365-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-3-lrg1-primary-antibodies-ihc-testing-3.jpgAnti-LRG1 Antibody Picoband® IHC analysis of LRG1 using anti-LRG1 antibody (A04365-3). LRG1 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LRG1 Antibody (A04365-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-3-lrg1-primary-antibodies-wb-testing-1_1.jpgAnti-LRG1 Antibody Picoband®Western blot analysis of LRG1 using anti-LRG1 antibody (A04365-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRG1 antigen affinity purified polyclonal antibody (A04365-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LRG1 at approximately 38 kDa. The expected band size for LRG1 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-3-lrg1-primary-antibodies-ihc-testing-1.jpgAnti-LRG1 Antibody Picoband®IHC analysis of LRG1 using anti-LRG1 antibody (A04365-3). LRG1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRG1 Antibody (A04365-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-3-lrg1-primary-antibodies-ihc-testing-2_1.jpgAnti-LRG1 Antibody Picoband®IHC analysis of LRG1 using anti-LRG1 antibody (A04365-3). LRG1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRG1 Antibody (A04365-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04365-3-lrg1-primary-antibodies-ihc-testing-3_1.jpgAnti-LRG1 Antibody Picoband®IHC analysis of LRG1 using anti-LRG1 antibody (A04365-3). LRG1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRG1 Antibody (A04365-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240102026-03-16T05:08:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09143-1-myh4-primary-antibodies-ihc-testing-1.jpgAnti-MYH4 AntibodyIHC analysis of MYH4 using anti-MYH4 antibody (A09143-1). MYH4 was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MYH4 Antibody (A09143-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09143-1-myh4-primary-antibodies-ihc-testing-2.jpgAnti-MYH4 AntibodyIHC analysis of MYH4 using anti-MYH4 antibody (A09143-1). MYH4 was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MYH4 Antibody (A09143-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240112026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240122026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240132026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240152026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240162026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240172026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07526-2-tdo2-primary-antibodies-wb-testing-1.jpgAnti-TDO2 Antibody Picoband®Western blot analysis of TDO2 using anti-TDO2 antibody (A07526-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates Lane 2: mouse liver tissue lysates, Lane 3: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TDO2 antigen affinity purified polyclonal antibody (A07526-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TDO2 at approximately 48 kDa. The expected band size for TDO2 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07526-2-tdo2-primary-antibodies-ihc-testing-1.jpgAnti-TDO2 Antibody Picoband®IHC analysis of TDO2 using anti-TDO2 antibody (A07526-2). TDO2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDO2 Antibody (A07526-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07526-2-tdo2-primary-antibodies-ihc-testing-2.jpgAnti-TDO2 Antibody Picoband®IHC analysis of TDO2 using anti-TDO2 antibody (A07526-2). TDO2 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TDO2 Antibody (A07526-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07526-2-tdo2-primary-antibodies-fcm-testing-1.jpgAnti-TDO2 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-TDO2 antibody (A07526-2). Overlay histogram showing HepG2 cells stained with A07526-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TDO2 Antibody (A07526-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240182026-03-13T05:05:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01898-3-c5ar1-primary-antibodies-wb-testing-1.jpgAnti-C5aR AntibodyWestern blot analysis of C5AR1 using anti-C5AR1 antibody (A01898-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human U251 whole cell lysates. Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C5AR1 antigen affinity purified polyclonal antibody (A01898-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for C5AR1 at approximately 45 kDa. The expected band size for C5AR1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01898-3-c5ar1-primary-antibodies-ihc-testing-1.jpgAnti-C5aR AntibodyIHC analysis of C5AR1 using anti-C5AR1 antibody (A01898-3). C5AR1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-C5AR1 Antibody (A01898-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240192026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240202026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05531-2-diaph3-primary-antibodies-wb-testing-1.jpgAnti-DIAPH3 Antibody Picoband®Western blot analysis of DIAPH3 using anti-DIAPH3 antibody (A05531-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DIAPH3 antigen affinity purified polyclonal antibody (A05531-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DIAPH3 at approximately 150 kDa. The expected band size for DIAPH3 is at 137 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05531-2-diaph3-primary-antibodies-if-testing-1.jpgAnti-DIAPH3 Antibody Picoband®IF analysis of DIAPH3 using anti-DIAPH3 antibody (A05531-2). DIAPH3 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DIAPH3 Antibody (A05531-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05531-2-diaph3-primary-antibodies-fcm-testing-1.jpgAnti-DIAPH3 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-DIAPH3 antibody (A05531-2). Overlay histogram showing 293T cells stained with A05531-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DIAPH3 Antibody (A05531-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240212026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00136-2-dnmt3a-primary-antibodies-wb-testing-1.jpgAnti-DNMT3A Antibody Picoband® Western blot analysis of DNMT3A using anti-DNMT3A antibody (A00136-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse testis tissue lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNMT3A antigen affinity purified polyclonal antibody (A00136-2) at 0.5 μg/ml overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNMT3A at approximately 120-130 kDa. The expected band size for DNMT3A is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00136-2-dnmt3a-primary-antibodies-ihc-testing-2.jpgAnti-DNMT3A Antibody Picoband® IHC analysis of DNMT3A using anti-DNMT3A antibody (A00136-2). DNMT3A was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNMT3A Antibody (A00136-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00136-2-dnmt3a-primary-antibodies-if-testing-3.jpgAnti-DNMT3A Antibody Picoband® IF analysis of DNMT3A using anti-DNMT3A antibody (A00136-2) and anti-Beta Tubulin antibody (M01857-3). DNMT3A was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DNMT3A Antibody (A00136-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00136-2-dnmt3a-primary-antibodies-ip-testing-4.jpgAnti-DNMT3A Antibody Picoband® Immunoprecipitating DNMT3A in MCF-7 whole cell lysate. Western blot analysis of DNMT3A using anti-DNMT3A antibody (A00136-2). Lane 1: MCF-7 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-DNMT3A antibody in MCF-7 whole cell lysate, Lane 3: anti-DNMT3A antibody (2μg) + MCF-7 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-DNMT3A antigen affinity purified polyclonal antibody (A00136-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for DNMT3A at approximately 120-130 kDa. The expected band size for DNMT3A is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00136-2-293t-cells-primary-antibodies-fcm-testing-5.jpgAnti-DNMT3A Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-293T cells antibody (A00136-2). Overlay histogram showing 293T cells stained with A00136-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-293T cells Antibody (A00136-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240222026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06212-2-eif3d-primary-antibodies-wb-testing-1.jpgAnti-EIF3D Antibody Picoband®Western blot analysis of EIF3D using anti-EIF3D antibody (A06212-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat RH35 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF3D antigen affinity purified polyclonal antibody (A06212-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EIF3D at approximately 55 kDa. The expected band size for EIF3D is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06212-2-eif3d-primary-antibodies-ihc-testing-1.jpgAnti-EIF3D Antibody Picoband®IHC analysis of EIF3D using anti-EIF3D antibody (A06212-2). EIF3D was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3D Antibody (A06212-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06212-2-eif3d-primary-antibodies-ihc-testing-2.jpgAnti-EIF3D Antibody Picoband®IHC analysis of EIF3D using anti-EIF3D antibody (A06212-2). EIF3D was detected in a paraffin-embedded section of human testicular cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3D Antibody (A06212-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240232026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240242026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240252026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240262026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05911-2-uso1-primary-antibodies-wb-testing-1.jpgAnti-p115/USO1 AntibodyWestern blot analysis of p115/USO1 using anti-p115/USO1 antibody (A05911-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-p115/USO1 antigen affinity purified polyclonal antibody (A05911-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for p115/USO1 at approximately 115 kDa. The expected band size for p115/USO1 is at 108 kDa. https://www.bosterbio.com/catalog/product/view/id/1240272026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240282026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240292026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240302026-03-13T05:05:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240312026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240322026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240332026-03-16T05:08:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06273-1-edil3-primary-antibodies-wb-testing-1.jpgAnti-EDIL3 Antibody Western blot analysis of EDIL3 using anti-EDIL3 antibody (A06273-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat NRK whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EDIL3 antigen affinity purified polyclonal antibody (A06273-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EDIL3 at approximately 54 kDa. The expected band size for EDIL3 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06273-1-edil3-primary-antibodies-ihc-testing-1.jpgAnti-EDIL3 AntibodyIHC analysis of EDIL3 using anti-EDIL3 antibody (A06273-1). EDIL3 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EDIL3 Antibody (A06273-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240342026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00690-3-ephb4-primary-antibodies-wb-testing-1.jpgAnti-EPHB4 Antibody Western blot analysis of EPHB4 using anti-EPHB4 antibody (A00690-3). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EPHB4 antigen affinity purified polyclonal antibody (A00690-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EPHB4 at approximately 108 kDa. The expected band size for EPHB4 is at 108 kDa. https://www.bosterbio.com/catalog/product/view/id/1240352026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240362026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240372026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02682-1-rab1a-primary-antibodies-wb-testing-1.jpgAnti-RAB1A AntibodyWestern blot analysis of RAB1A using anti-RAB1A antibody (A02682-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB1A antigen affinity purified polyclonal antibody (A02682-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RAB1A at approximately 23 kDa. The expected band size for RAB1A is at 23 kDa. https://www.bosterbio.com/catalog/product/view/id/1240382026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240392026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240402026-04-02T05:00:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10278-1-timm44-primary-antibodies-wb-testing-1.jpgAnti-TIMM44 Antibody Picoband®Western blot analysis of TIMM44 using anti-TIMM44 antibody (A10278-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIMM44 antigen affinity purified polyclonal antibody (A10278-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TIMM44 at approximately 44 kDa. The expected band size for TIMM44 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10278-1-timm44-primary-antibodies-ihc-testing-1.jpgAnti-TIMM44 Antibody Picoband®IHC analysis of TIMM44 using anti-TIMM44 antibody (A10278-1). TIMM44 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TIMM44 Antibody (A10278-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10278-1-timm44-primary-antibodies-ihc-testing-2.jpgAnti-TIMM44 Antibody Picoband®IHC analysis of TIMM44 using anti-TIMM44 antibody (A10278-1). TIMM44 was detected in a paraffin-embedded section of human lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TIMM44 Antibody (A10278-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10278-1-timm44-primary-antibodies-if-testing-1.jpgAnti-TIMM44 Antibody Picoband®IF analysis of TIMM44 using anti-TIMM44 antibody (A10278-1). TIMM44 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TIMM44 Antibody (A10278-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1240412026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240422026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240432026-03-17T05:15:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07140-1-1-slc27a2-primary-antibodies-wb-testing-1.jpgAnti-FATP2/SLC27A2 Antibody Picoband®Western blot analysis of FATP2/SLC27A2 using anti-FATP2/SLC27A2 antibody (A07140-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FATP2/SLC27A2 antigen affinity purified polyclonal antibody (A07140-1) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FATP2/SLC27A2 at approximately 70 kDa. The expected band size for FATP2/SLC27A2 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07140-1-slc27a2-primary-antibodies-wb-testing-1.jpgAnti-FATP2/SLC27A2 Antibody Picoband®Western blot analysis of FATP2/SLC27A2 using anti-FATP2/SLC27A2 antibody (A07140-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human HL-60 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: rat NRK whole cell lysates, Lane 6: mouse liver tissue lysates Lane 7: mouse kidney tissue lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FATP2/SLC27A2 antigen affinity purified polyclonal antibody (A07140-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FATP2/SLC27A2 at approximately 70 kDa. The expected band size for FATP2/SLC27A2 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07140-1-slc27a2-primary-antibodies-ihc-testing-1.jpgAnti-FATP2/SLC27A2 Antibody Picoband®IHC analysis of FATP2/SLC27A2 using anti-FATP2/SLC27A2 antibody (A07140-1). FATP2/SLC27A2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FATP2/SLC27A2 Antibody (A07140-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07140-1-slc27a2-primary-antibodies-ihc-testing-2.jpgAnti-FATP2/SLC27A2 Antibody Picoband®IHC analysis of FATP2/SLC27A2 using anti-FATP2/SLC27A2 antibody (A07140-1). FATP2/SLC27A2 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FATP2/SLC27A2 Antibody (A07140-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07140-1-slc27a2-primary-antibodies-fcm-testing-1.jpgAnti-FATP2/SLC27A2 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-FATP2/SLC27A2 antibody (A07140-1). Overlay histogram showing HepG2 cells stained with A07140-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-FATP2/SLC27A2 Antibody (A07140-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240442026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00406-2-fbxw7-primary-antibodies-wb-testing-1.jpgAnti-FBXW7 Antibody Picoband® Western blot analysis of FBXW7 using anti-FBXW7 antibody (A00406-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Nih/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FBXW7 antigen affinity purified polyclonal antibody (A00406-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FBXW7 at approximately 75 kDa. The expected band size for FBXW7 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00406-2-fbxw7-primary-antibodies-fcm-testing-2.jpgAnti-FBXW7 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-FBXW7 antibody (A00406-2). Overlay histogram showing HepG2 cells stained with A00406-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FBXW7 Antibody (A00406-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240452026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240462026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240472026-03-16T05:08:15+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240482026-03-16T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04733-2-mtf1-primary-antibodies-wb-testing-1.jpgAnti-MTF1 Antibody Western blot analysis of MTF1 using anti-MTF1 antibody (A04733-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTF1 antigen affinity purified polyclonal antibody (A04733-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MTF1 at approximately 70 kDa. The expected band size for MTF1 is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04733-2-mtf1-primary-antibodies-ihc-testing-1.jpgAnti-MTF1 AntibodyIHC analysis of MTF1 using anti-MTF1 antibody (A04733-2). MTF1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTF1 Antibody (A04733-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240492026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02120-3-cd73-nt5e-primary-antibodies-wb-testing-1.jpgAnti-CD73/NT5E Antibody Western blot analysis of CD73/NT5E using anti-CD73/NT5E antibody (A02120-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human HUH-7 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat RH-35 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD73/NT5E antigen affinity purified polyclonal antibody (A02120-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD73/NT5E at approximately 70 kDa. The expected band size for CD73/NT5E is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02120-3-gr4.jpgAnti-CD73/NT5E AntibodySSD treatment ameliorated RA rats. Representative images of hind paws from different groups and changes in foot circumference. Hematoxylin eosin staining and immunohistochemical staining (CD31, CD39, CD73, CCR6 and IL1R1) of knee joint synovial slices. *P < 0.05, **P < 0.01 vs Model group. Index in PubMed under a CC BY license. PMID: <a href='https://www.cell.com/heliyon/fulltext/S2405-8440(24)13288-4'>39296024</a> https://www.bosterbio.com/catalog/product/view/id/1240502026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-wb-testing-1.jpgAnti-P4HA1 Antibody Picoband® Western blot analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P4HA1 antigen affinity purified polyclonal antibody (A05917-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P4HA1 at approximately 61 kDa. The expected band size for P4HA1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-ihc-testing-2.jpgAnti-P4HA1 Antibody Picoband® IHC analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). P4HA1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-P4HA1 Antibody (A05917-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-ihc-testing-3.jpgAnti-P4HA1 Antibody Picoband® IHC analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). P4HA1 was detected in a paraffin-embedded section of human invasive urothelial carcinoma of the bladder with squamous differentiation tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-P4HA1 Antibody (A05917-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-ihc-testing-4.jpgAnti-P4HA1 Antibody Picoband® IHC analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). P4HA1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-P4HA1 Antibody (A05917-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-wb-testing-1_1.jpgAnti-P4HA1 Antibody Picoband®Western blot analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P4HA1 antigen affinity purified polyclonal antibody (A05917-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P4HA1 at approximately 61 kDa. The expected band size for P4HA1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-ihc-testing-1.jpgAnti-P4HA1 Antibody Picoband®IHC analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). P4HA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-P4HA1 Antibody (A05917-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-ihc-testing-2_1.jpgAnti-P4HA1 Antibody Picoband®IHC analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). P4HA1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-P4HA1 Antibody (A05917-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05917-2-p4ha1-primary-antibodies-if-testing-1.jpgAnti-P4HA1 Antibody Picoband®IF analysis of P4HA1 using anti-P4HA1 antibody (A05917-2). P4HA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-P4HA1 Antibody (A05917-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1240512026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03550-1-pdcd6-primary-antibodies-wb-testing-1.jpgAnti-ALG2/PDCD6 Antibody Picoband®Western blot analysis of ALG2/PDCD6 using anti-ALG2/PDCD6 antibody (A03550-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat small intestine tissue lysates, Lane 7: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALG2/PDCD6 antigen affinity purified polyclonal antibody (A03550-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALG2/PDCD6 at approximately 17 kDa. The expected band size for ALG2/PDCD6 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03550-1-pdcd6-primary-antibodies-fcm-testing-1.jpgAnti-ALG2/PDCD6 Antibody Picoband®Flow Cytometry analysis of PC-3 cells using anti-ALG2/PDCD6 antibody (A03550-1). Overlay histogram showing PC-3 cells stained with A03550-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ALG2/PDCD6 Antibody (A03550-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240522026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240532026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11544-1-trim44-primary-antibodies-wb-testing-1.jpgAnti-TRIM44 Antibody Picoband®Western blot analysis of TRIM44 using anti-TRIM44 antibody (A11544-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIM44 antigen affinity purified polyclonal antibody (A11544-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIM44 at approximately 50 kDa. The expected band size for TRIM44 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11544-1-trim44-primary-antibodies-fcm-testing-1.jpgAnti-TRIM44 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-TRIM44 antibody (A11544-1). Overlay histogram showing MCF-7 cells stained with A11544-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TRIM44 Antibody (A11544-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240542026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04080-1-arl3-primary-antibodies-wb-testing-1.jpgAnti-ARL3 Antibody Picoband® Western blot analysis of ARL3 using anti-ARL3 antibody (A04080-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARL3 antigen affinity purified polyclonal antibody (Catalog # A04080-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARL3 at approximately 23 kDa. The expected band size for ARL3 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04080-1-arl3-primary-antibodies-if-testing-2.jpgAnti-ARL3 Antibody Picoband® IF analysis of ARL3 using anti-ARL3 antibody (A04080-1) and anti-Beta Tubulin antibody (M01857-3). ARL3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ARL3 Antibody (A04080-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04080-1-arl3-primary-antibodies-fcm-testing-3.jpgAnti-ARL3 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-ARL3 antibody (A04080-1). Overlay histogram showing SH-SY5Y cells stained with A04080-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARL3 Antibody (A04080-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240552026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02073-4-cd42b-gp1ba-primary-antibodies-wb-testing-1.jpgAnti-CD42b/GP1BA Antibody Western blot analysis of CD42b/GP1BA using anti-CD42b/GP1BA antibody (A02073-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD42b/GP1BA antigen affinity purified polyclonal antibody (A02073-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD42b/GP1BA at approximately 58 kDa. The expected band size for CD42b/GP1BA is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02073-4-cd42b-gp1ba-primary-antibodies-ihc-testing-2.jpgAnti-CD42b/GP1BA Antibody IHC analysis of CD42b/GP1BA using anti-CD42b/GP1BA antibody (A02073-4). CD42b/GP1BA was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD42b/GP1BA Antibody (A02073-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240562026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-wb-testing-1.jpgAnti-CLTA Antibody Picoband® Western blot analysis of CLTA using anti-CLTA antibody (A05796-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLTA antigen affinity purified polyclonal antibody (A05796-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CLTA at approximately 28-30 kDa. The expected band size for CLTA is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-ihc-testing-2.jpgAnti-CLTA Antibody Picoband® IHC analysis of CLTA using anti-CLTA antibody (A05796-3). CLTA was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CLTA Antibody (A05796-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-ihc-testing-3.jpgAnti-CLTA Antibody Picoband® IHC analysis of CLTA using anti-CLTA antibody (A05796-3). CLTA was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CLTA Antibody (A05796-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-ihc-testing-4.jpgAnti-CLTA Antibody Picoband® IHC analysis of CLTA using anti-CLTA antibody (A05796-3). CLTA was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CLTA Antibody (A05796-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-if-testing-5.jpgAnti-CLTA Antibody Picoband® IF analysis of CLTA using anti-CLTA antibody (A05796-3). CLTA was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-CLTA Antibody (A05796-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-wb-testing-1_1.jpgAnti-CLTA Antibody Picoband®Western blot analysis of CLTA using anti-CLTA antibody (A05796-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLTA antigen affinity purified polyclonal antibody (A05796-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CLTA at approximately 30 kDa. The expected band size for CLTA is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-ihc-testing-1.jpgAnti-CLTA Antibody Picoband®IHC analysis of CLTA using anti-CLTA antibody (A05796-3). CLTA was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLTA Antibody (A05796-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-if-testing-1.jpgAnti-CLTA Antibody Picoband®IF analysis of CLTA using anti-CLTA antibody (A05796-3). CLTA was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CLTA Antibody (A05796-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05796-3-clta-primary-antibodies-fcm-testing-1.jpgAnti-CLTA Antibody Picoband®Flow Cytometry analysis of HL-60 cells using anti-CLTA antibody (A05796-3). Overlay histogram showing HL-60 cells stained with A05796-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CLTA Antibody (A05796-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240572026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240582026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240592026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240602026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240612026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240622026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-wb-testing-1.jpgAnti-MIRO2/RHOT2 Antibody Picoband® Western blot analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIRO2/RHOT2 antigen affinity purified polyclonal antibody (A08801-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MIRO2/RHOT2 at approximately 80 kDa. The expected band size for MIRO2/RHOT2 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-ihc-testing-2.jpgAnti-MIRO2/RHOT2 Antibody Picoband® IHC analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1). MIRO2/RHOT2 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIRO2/RHOT2 Antibody (A08801-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-ihc-testing-3.jpgAnti-MIRO2/RHOT2 Antibody Picoband® IHC analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1). MIRO2/RHOT2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIRO2/RHOT2 Antibody (A08801-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-ihc-testing-4.jpgAnti-MIRO2/RHOT2 Antibody Picoband® IHC analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1). MIRO2/RHOT2 was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIRO2/RHOT2 Antibody (A08801-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-ihc-testing-5.jpgAnti-MIRO2/RHOT2 Antibody Picoband® IHC analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1). MIRO2/RHOT2 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIRO2/RHOT2 Antibody (A08801-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-ihc-testing-6.jpgAnti-MIRO2/RHOT2 Antibody Picoband® IHC analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1). MIRO2/RHOT2 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIRO2/RHOT2 Antibody (A08801-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-if-testing-7.jpgAnti-MIRO2/RHOT2 Antibody Picoband® IF analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1) and anti-Tubulin Alpha antibody (M03989-3). MIRO2/RHOT2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MIRO2/RHOT2 Antibody (A08801-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-ip-testing-8.jpgAnti-MIRO2/RHOT2 Antibody Picoband® Immunoprecipitating (IP) MIRO2/RHOT2 in MCF-7 whole cell lysate. Western blot analysis of MIRO2/RHOT2 using anti-MIRO2/RHOT2 antibody (A08801-1); Lane 1: MCF-7 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-MIRO2/RHOT2 antibody in MCF-7 whole cell lysate; Lane 3: anti-MIRO2/RHOT2 antibody (2μg) + MCF-7 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MIRO2/RHOT2 antigen affinity purified polyclonal antibody (A08801-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for MIRO2/RHOT2 at approximately 80 kDa. The expected band size for MIRO2/RHOT2 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08801-1-rhot2-primary-antibodies-fcm-testing-9.jpgAnti-MIRO2/RHOT2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MIRO2/RHOT2 antibody (A08801-1). Overlay histogram showing MCF-7 cells stained with A08801-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MIRO2/RHOT2 Antibody (A08801-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240632026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240642026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240652026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-3-nras-primary-antibodies-wb-testing-1.jpgAnti-NRAS Antibody Picoband®Western blot analysis of NRAS using anti-NRAS antibody (A00099-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NRAS antigen affinity purified polyclonal antibody (A00099-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NRAS at approximately 21 kDa. The expected band size for NRAS is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-3-nras-primary-antibodies-ihc-testing-1.jpgAnti-NRAS Antibody Picoband®IHC analysis of NRAS using anti-NRAS antibody (A00099-3). NRAS was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRAS Antibody (A00099-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-3-nras-primary-antibodies-ihc-testing-2.jpgAnti-NRAS Antibody Picoband®IHC analysis of NRAS using anti-NRAS antibody (A00099-3). NRAS was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRAS Antibody (A00099-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-3-nras-primary-antibodies-ihc-testing-3.jpgAnti-NRAS Antibody Picoband®IHC analysis of NRAS using anti-NRAS antibody (A00099-3). NRAS was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRAS Antibody (A00099-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-3-nras-primary-antibodies-ihc-testing-4.jpgAnti-NRAS Antibody Picoband®IHC analysis of NRAS using anti-NRAS antibody (A00099-3). NRAS was detected in a paraffin-embedded section of human lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRAS Antibody (A00099-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-3-nras-primary-antibodies-fcm-testing-1.jpgAnti-NRAS Antibody Picoband®Flow Cytometry analysis of C6 cells using anti-NRAS antibody (A00099-3). Overlay histogram showing C6 cells stained with A00099-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NRAS Antibody (A00099-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00099-3-nras-primary-antibodies-fcm-testing-2.jpgAnti-NRAS Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-NRAS antibody (A00099-3). Overlay histogram showing MCF-7 cells stained with A00099-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NRAS Antibody (A00099-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240662026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240672026-03-16T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06782-2-slc38a3-primary-antibodies-wb-testing-1.jpgAnti-SLC38A3 Antibody Western blot analysis of SLC38A3 using anti-SLC38A3 antibody (A06782-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC38A3 antigen affinity purified polyclonal antibody (A06782-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC38A3 at approximately 70 kDa. The expected band size for SLC38A3 is at 56 kDa. https://www.bosterbio.com/catalog/product/view/id/1240682026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240692026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240702026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02691-2-cyp26b1-primary-antibodies-wb-testing-1.jpgAnti-CYP26B1 Antibody Picoband®Western blot analysis of CYP26B1 using anti-CYP26B1 antibody (A02691-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U2OS whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYP26B1 antigen affinity purified polyclonal antibody (A02691-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CYP26B1 at approximately 58 kDa. The expected band size for CYP26B1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02691-2-cyp26b1-primary-antibodies-ihc-testing-1.jpgAnti-CYP26B1 Antibody Picoband®IHC analysis of CYP26B1 using anti-CYP26B1 antibody (A02691-2). CYP26B1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CYP26B1 Antibody (A02691-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02691-2-cyp26b1-primary-antibodies-ihc-testing-2.jpgAnti-CYP26B1 Antibody Picoband®IHC analysis of CYP26B1 using anti-CYP26B1 antibody (A02691-2). CYP26B1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CYP26B1 Antibody (A02691-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02691-2-cyp26b1-primary-antibodies-if-testing-1.jpgAnti-CYP26B1 Antibody Picoband®IF analysis of CYP26B1 using anti-CYP26B1 antibody (A02691-2). CYP26B1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CYP26B1 Antibody (A02691-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02691-2-cyp26b1-primary-antibodies-fcm-testing-1.jpgAnti-CYP26B1 Antibody Picoband®Flow Cytometry analysis of JK cells using anti-CYP26B1 antibody (A02691-2). Overlay histogram showing JK cells stained with A02691-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CYP26B1 Antibody (A02691-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240712026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240722026-03-16T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06081-2-mlph-primary-antibodies-ihc-testing-1.jpgAnti-Melanophilin/MLPH AntibodyIHC analysis of Melanophilin/MLPH using anti-Melanophilin/MLPH antibody (A06081-2). Melanophilin/MLPH was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Melanophilin/MLPH Antibody (A06081-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06081-2-mlph-primary-antibodies-ihc-testing-2.jpgAnti-Melanophilin/MLPH AntibodyIHC analysis of Melanophilin/MLPH using anti-Melanophilin/MLPH antibody (A06081-2). Melanophilin/MLPH was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Melanophilin/MLPH Antibody (A06081-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1240732026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00269-3-mitf-primary-antibodies-wb-testing-1.jpgAnti-MITF Antibody Picoband® Western blot analysis of MITF using anti-MITF antibody (A00269-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MITF antigen affinity purified polyclonal antibody (A00269-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MITF at approximately 75 kDa. The expected band size for MITF is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00269-3-1-s2.0-s2405844024027464-gr6.jpgAnti-MITF Antibody Picoband®WBS inhibited the expression of TYR (A), TYRP-1 (B), TYRP-2 (C) and MITF (D) in B16F10 cells. Levels of MITF (E), TYRP-1 (F) and TYRP-2 (G) proteins in B16F10 cells treated with WBS as determined by western blotting. GAPDH was a loading control (H). The data are expressed as the mean ± S.E.M. and were analyzed by one-way. Significance was defined as *p<0.05, **p<0.01, ***p<0.001 and ****p<0.0001. Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2405844024027464'>38455547</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00269-3-mitf-primary-antibodies-wb-testing-1_1.jpgAnti-MITF Antibody Picoband®Western blot analysis of MITF using anti-MITF antibody (A00269-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MITF antigen affinity purified polyclonal antibody (A00269-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MITF at approximately 70 kDa. The expected band size for MITF is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00269-3-mitf-primary-antibodies-fcm-testing-1.jpgAnti-MITF Antibody Picoband®Flow Cytometry analysis of K562 cells using anti-MITF antibody (A00269-3). Overlay histogram showing K562 cells stained with A00269-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MITF Antibody (A00269-3, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240742026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240752026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240762026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240772026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02613-1-pdcd5-primary-antibodies-wb-testing-1.jpgAnti-PDCD5 Antibody Western blot analysis of PDCD5 using anti-PDCD5 antibody (A02613-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: human SiHa whole cell lysates, Lane 6: human Hela whole cell lysates, Lane 7: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDCD5 antigen affinity purified polyclonal antibody (A02613-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDCD5 at approximately 14 kDa. The expected band size for PDCD5 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02613-1-pdcd5-primary-antibodies-ihc-testing-1.jpgAnti-PDCD5 AntibodyIHC analysis of PDCD5 using anti-PDCD5 antibody (A02613-1). PDCD5 was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDCD5 Antibody (A02613-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02613-1-12967_2014_article_287_fig2_html.jpgAnti-PDCD5 AntibodyMethylating effect of daphnetin and 5-aza-dc on DR3, PDCD5, FasL and p53 in CIA rat synovial cells. Four experimental groups consisting of untreated cell control, or treated with 5-aza-dc at 20 μM, daphnetin at 40 μg/mL, or combination of 5-aza-dc (20 μM) and daphnetin (40 μg/mL). Cells were cultured, treated and harvested as described in Materials and Methods. Total DNA was extracted and used for MSP after bisulphite modification. M: methylated amplification products, U: hypomethylated amplification products. Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-014-0287-x'>25311560</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02613-1-12967_2014_article_287_fig3_html.jpgAnti-PDCD5 AntibodyEffect of daphnetin and 5-aza-dc on expression of DR3, PDCD5, FasL, p53 (A) and DNMT1, DNMT3a, DNMT3b (B) in CIA rat synovial cells. Four experimental groups consisting of untreated cell control, or treated with 5-aza-dc at 20 μM, daphnetin at 40 μg/mL, or combination of 5-aza-dc (20 μM) and daphnetin (40 μg/mL). Cells were cultured, treated and harvested as described in Matreials and Methods. Total RNA was extracted and cDNA was synthesized. After reverse transcription, cDNA was used for real time-PCR. Relative quantification of gene expression was performed by the 2-ΔΔCt method. The results show the mean ± S.D. of six independent experiments. ▲P < 0.05 compared with control, ●P < 0.05 compared with 5-aza-dc, ☆P > 0.05 compared with 5-aza-dc, ★P > 0.05 compared with daphnetin, *P < 0.05 compared with daphnetin. Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-014-0287-x'>25311560</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02613-1-12967_2014_article_287_fig4_html.jpgAnti-PDCD5 AntibodyEffect of daphnetin on DR3, PDCD5, FasL and p53 protein expression in CIA rats synovial cells. Cells were cultured, treated and harvested as described Materials and Methods. Four experimental groups consisting of untreated cell control, 5-aza-dc at 20 μM, daphnetin at 40 μg/mL, or combination of 5-aza-dc (20 μM) and daphnetin (40 μg/mL). The results show the mean ± S.D. of six independent experiments. ▲P < 0.05 compared with control, ●P < 0.05 compared with 5-aza-dc, ★P > 0.05 compared with 5-aza-dc, *P < 0.05 compared with daphnetin. Index in PubMed under a CC BY license. PMID: <a href='https://link.springer.com/article/10.1186/s12967-014-0287-x'>25311560</a> https://www.bosterbio.com/catalog/product/view/id/1240782026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240792026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240802026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08642-d2hgdh-primary-antibodies-wb-testing-1.jpgAnti-D2HGDH Antibody Picoband®Western blot analysis of D2HGDH using anti-D2HGDH antibody (A08642). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-D2HGDH antigen affinity purified polyclonal antibody (A08642) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for D2HGDH at approximately 56 kDa. The expected band size for D2HGDH is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08642-d2hgdh-primary-antibodies-if-testing-1.jpgAnti-D2HGDH Antibody Picoband®IF analysis of D2HGDH using anti-D2HGDH antibody (A08642). D2HGDH was detected in an immunocytochemical section of SIHA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-D2HGDH Antibody (A08642) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1240812026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09447-1-fbxo22-primary-antibodies-wb-testing-1.jpgAnti-FBXO22 Antibody Picoband®Western blot analysis of FBXO22 using anti-FBXO22 antibody (A09447-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FBXO22 antigen affinity purified polyclonal antibody (A09447-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FBXO22 at approximately 42 kDa. The expected band size for FBXO22 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09447-1-fbxo22-primary-antibodies-ihc-testing-1.jpgAnti-FBXO22 Antibody Picoband®IHC analysis of FBXO22 using anti-FBXO22 antibody (A09447-1). FBXO22 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FBXO22 Antibody (A09447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09447-1-fbxo22-primary-antibodies-ihc-testing-2.jpgAnti-FBXO22 Antibody Picoband®IHC analysis of FBXO22 using anti-FBXO22 antibody (A09447-1). FBXO22 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FBXO22 Antibody (A09447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09447-1-fbxo22-primary-antibodies-ihc-testing-3.jpgAnti-FBXO22 Antibody Picoband®IHC analysis of FBXO22 using anti-FBXO22 antibody (A09447-1). FBXO22 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FBXO22 Antibody (A09447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09447-1-fbxo22-primary-antibodies-ihc-testing-4.jpgAnti-FBXO22 Antibody Picoband®IHC analysis of FBXO22 using anti-FBXO22 antibody (A09447-1). FBXO22 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FBXO22 Antibody (A09447-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09447-1-fbxo22-primary-antibodies-ip-testing-1.jpgAnti-FBXO22 Antibody Picoband®Immunoprecipitating FBXO22 in Hela whole cell lysate. Western blot analysis of FBXO22 using anti-FBXO22 antibody (A09447-1). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-FBXO22 antibody in Hela whole cell lysate, Lane 3: anti-FBXO22 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FBXO22 antigen affinity purified polyclonal antibody (A09447-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for FBXO22 at approximately 42 kDa. The expected band size for FBXO22 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09447-1-fbxo22-primary-antibodies-fcm-testing-1.jpgAnti-FBXO22 Antibody Picoband®Flow Cytometry analysis of Hela cells using anti-FBXO22 antibody (A09447-1). Overlay histogram showing Hela cells stained with A09447-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FBXO22 Antibody (A09447-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1240822026-03-16T05:08:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08205-1-hbxip-primary-antibodies-wb-testing-1.jpgAnti-HBXIP Antibody Western blot analysis of HBXIP using anti-HBXIP antibody (A08205-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HBXIP antigen affinity purified polyclonal antibody (A08205-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HBXIP at approximately 12 kDa. The expected band size for HBXIP is at 10 kDa. https://www.bosterbio.com/catalog/product/view/id/1240832026-03-16T05:08:16+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240842026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1240852026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07559-4-1-s2.0-s168785072500740x-gr12.jpgAnti-ACAA1 Antibody Picoband®IHC analysis of 4 prognostic genes in clinical samples. Index in Journal of Radiation Research and Applied Sciences under a CC BY license. DOI: <a href='https://www.sciencedirect.com/science/article/pii/S168785072500740X'>10.1016/j.jrras.2025.102028</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07559-4-acaa1-primary-antibodies-wb-testing-1.jpgAnti-ACAA1 Antibody Picoband®Western blot analysis of ACAA1 using anti-ACAA1 antibody (A07559-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACAA1 antigen affinity purified polyclonal antibody (A07559-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ACAA1 at approximately 41 kDa. The expected band size for ACAA1 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07559-4-acaa1-primary-antibodies-ihc-testing-1.jpgAnti-ACAA1 Antibody Picoband®IHC analysis of ACAA1 using anti-ACAA1 antibody (A07559-4). ACAA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACAA1 Antibody (A07559-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07559-4-acaa1-primary-antibodies-ihc-testing-2.jpgAnti-ACAA1 Antibody Picoband®IHC analysis of ACAA1 using anti-ACAA1 antibody (A07559-4). ACAA1 was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACAA1 Antibody (A07559-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07559-4-acaa1-primary-antibodies-if-testing-1.jpgAnti-ACAA1 Antibody Picoband®IF analysis of ACAA1 using anti-ACAA1 antibody (A07559-4). ACAA1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ACAA1 Antibody (A07559-4) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-mettl11a-ntmt1-picoband-trade-antibody-a10023-1-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10023-1-ntmt1-primary-antibodies-wb-testing-1.jpgAnti-METTL11A/NTMT1 Antibody Picoband® Western blot analysis of METTL11A/NTMT1 using anti-METTL11A/NTMT1 antibody (A10023-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METTL11A/NTMT1 antigen affinity purified polyclonal antibody (Catalog # A10023-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METTL11A/NTMT1 at approximately 25 kDa. The expected band size for METTL11A/NTMT1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10023-1-ntmt1-primary-antibodies-ihc-testing-2.jpgAnti-METTL11A/NTMT1 Antibody Picoband® IHC analysis of METTL11A/NTMT1 using anti-METTL11A/NTMT1 antibody (A10023-1). METTL11A/NTMT1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METTL11A/NTMT1 Antibody (A10023-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10023-1-ntmt1-primary-antibodies-ihc-testing-3.jpgAnti-METTL11A/NTMT1 Antibody Picoband® IHC analysis of METTL11A/NTMT1 using anti-METTL11A/NTMT1 antibody (A10023-1). METTL11A/NTMT1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METTL11A/NTMT1 Antibody (A10023-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10023-1-ntmt1-primary-antibodies-if-testing-4.jpgAnti-METTL11A/NTMT1 Antibody Picoband® IF analysis of METTL11A/NTMT1 using anti-METTL11A/NTMT1 antibody (A10023-1) and anti-Beta Tubulin antibody (M01857-3). METTL11A/NTMT1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-METTL11A/NTMT1 Antibody (A10023-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10023-1-ntmt1-primary-antibodies-fcm-testing-5.pngAnti-METTL11A/NTMT1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-METTL11A/NTMT1 antibody (A10023-1). Overlay histogram showing HepG2 cells stained with A10023-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-METTL11A/NTMT1 Antibody (A10023-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-muc3a-b-picoband-trade-antibody-a08332-1-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08332-1-muc3a3b-primary-antibodies-wb-testing-1.jpgAnti-MUC3A/B Antibody Picoband® Western blot analysis of MUC3A/B using anti-MUC3A/B antibody (A08332-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SW620 whole cell lysates, Lane 2: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MUC3A/B antigen affinity purified polyclonal antibody (Catalog # A08332-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MUC3A/B at approximately 345 kDa. The expected band size for MUC3A/B is at 345 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08332-1-muc3a3b-primary-antibodies-if-testing-2.jpgAnti-MUC3A/B Antibody Picoband® IF analysis of MUC3A/B using anti-MUC3A/B antibody (A08332-1). MUC3A/B was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MUC3A/B Antibody (A08332-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-nsg1-picoband-trade-antibody-a12107-1-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12107-1-nsg1-primary-antibodies-wb-testing-1.jpgAnti-NSG1 Antibody Picoband® Western blot analysis of NSG1 using anti-NSG1 antibody (A12107-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSG1 antigen affinity purified polyclonal antibody (Catalog # A12107-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSG1 at approximately 21 kDa. The expected band size for NSG1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12107-1-nsg1-primary-antibodies-ihc-testing-2.jpgAnti-NSG1 Antibody Picoband® IHC analysis of NSG1 using anti-NSG1 antibody (A12107-1). NSG1 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSG1 Antibody (A12107-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12107-1-nsg1-primary-antibodies-ihc-testing-3.jpgAnti-NSG1 Antibody Picoband® IHC analysis of NSG1 using anti-NSG1 antibody (A12107-1). NSG1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSG1 Antibody (A12107-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12107-1-nsg1-primary-antibodies-ihc-testing-4.jpgAnti-NSG1 Antibody Picoband® IHC analysis of NSG1 using anti-NSG1 antibody (A12107-1). NSG1 was detected in a paraffin-embedded section of human large B-cell lymphoma of the colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSG1 Antibody (A12107-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12107-1-nsg1-primary-antibodies-fcm-testing-5.pngAnti-NSG1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-NSG1 antibody (A12107-1). Overlay histogram showing JK cells stained with A12107-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSG1 Antibody (A12107-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-marchf2-picoband-trade-antibody-a13497-2-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13497-2-march2-primary-antibodies-wb-testing-1.jpgAnti-MARCHF2 Antibody Picoband® Western blot analysis of MARCHF2 using anti-MARCHF2 antibody (A13497-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MARCHF2 antigen affinity purified polyclonal antibody (Catalog # A13497-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MARCHF2 at approximately 27 kDa. The expected band size for MARCHF2 is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13497-2-march2-primary-antibodies-if-testing-2.jpgAnti-MARCHF2 Antibody Picoband® IF analysis of MARCHF2 using anti-MARCHF2 antibody (A13497-2). MARCHF2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MARCHF2 Antibody (A13497-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-nxpe3-picoband-trade-antibody-a18151-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18151-nxpe3-primary-antibodies-wb-testing-1.jpgAnti-NXPE3 Antibody Picoband® Western blot analysis of NXPE3 using anti-NXPE3 antibody (A18151). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NXPE3 antigen affinity purified polyclonal antibody (Catalog # A18151) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NXPE3 at approximately 90 kDa. The expected band size for NXPE3 is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18151-nxpe3-primary-antibodies-ihc-testing-1.jpgAnti-NXPE3 Antibody Picoband®IHC analysis of NXPE3 using anti-NXPE3 antibody (A18151). NXPE3 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NXPE3 Antibody (A18151) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18151-nxpe3-primary-antibodies-if-testing-2.jpgAnti-NXPE3 Antibody Picoband® IF analysis of NXPE3 using anti-NXPE3 antibody (A18151). NXPE3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NXPE3 Antibody (A18151) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18151-nxpe3-primary-antibodies-fcm-testing-3.pngAnti-NXPE3 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-NXPE3 antibody (A18151). Overlay histogram showing THP-1 cells stained with A18151 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NXPE3 Antibody (A18151, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nt5dc2-picoband-trade-antibody-a16483-1-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16483-1-nt5dc2-primary-antibodies-wb-testing-1.jpgAnti-NT5DC2 Antibody Picoband® Western blot analysis of NT5DC2 using anti-NT5DC2 antibody (A16483-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NT5DC2 antigen affinity purified polyclonal antibody (Catalog # A16483-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NT5DC2 at approximately 61 kDa. The expected band size for NT5DC2 is at 61 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nt5dc3-picoband-trade-antibody-a15406-1-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15406-1-nt5dc3-primary-antibodies-wb-testing-1.jpgAnti-NT5DC3 Antibody Picoband® Western blot analysis of NT5DC3 using anti-NT5DC3 antibody (A15406-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NT5DC3 antigen affinity purified polyclonal antibody (Catalog # A15406-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NT5DC3 at approximately 55 kDa. The expected band size for NT5DC3 is at 63,55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15406-1-nt5dc3-primary-antibodies-fcm-testing-2.pngAnti-NT5DC3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-NT5DC3 antibody (A15406-1). Overlay histogram showing U251 cells stained with A15406-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NT5DC3 Antibody (A15406-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nthl1-picoband-trade-antibody-a03207-2-boster.html2026-03-17T05:15:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03207-2-nthl1-primary-antibodies-wb-testing-1.jpgAnti-NTHL1 Antibody Picoband® Western blot analysis of NTHL1 using anti-NTHL1 antibody (A03207-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NTHL1 antigen affinity purified polyclonal antibody (Catalog # A03207-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NTHL1 at approximately 34 kDa. The expected band size for NTHL1 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03207-2-nthl1-primary-antibodies-if-testing-2.jpgAnti-NTHL1 Antibody Picoband® IF analysis of NTHL1 using anti-NTHL1 antibody (A03207-2) and anti-Beta Tubulin antibody (M01857-3). NTHL1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NTHL1 Antibody (A03207-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03207-2-nthl1-primary-antibodies-fcm-testing-3.pngAnti-NTHL1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-NTHL1 antibody (A03207-2). Overlay histogram showing MCF-7 cells stained with A03207-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NTHL1 Antibody (A03207-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ntn3-picoband-trade-antibody-a17692-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17692-ntn3-primary-antibodies-wb-testing-1.jpgAnti-NTN3 Antibody Picoband® Western blot analysis of NTN3 using anti-NTN3 antibody (A17692). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NTN3 antigen affinity purified polyclonal antibody (Catalog # A17692) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NTN3 at approximately 70 kDa. The expected band size for NTN3 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17692-ntn3-primary-antibodies-ihc-testing-2.jpgAnti-NTN3 Antibody Picoband® IHC analysis of NTN3 using anti-NTN3 antibody (A17692). NTN3 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NTN3 Antibody (A17692) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17692-ntn3-primary-antibodies-if-testing-3.jpgAnti-NTN3 Antibody Picoband® IF analysis of NTN3 using anti-NTN3 antibody (A17692). NTN3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NTN3 Antibody (A17692) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-nub1-picoband-trade-antibody-a06089-2-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06089-2-nub1-primary-antibodies-wb-testing-1.jpgAnti-NUB1 Antibody Picoband® Western blot analysis of NUB1 using anti-NUB1 antibody (A06089-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Colo320 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human Raji whole cell lysates, Lane 6: monkey COS-7 whole cell lysates, Lane 8: human MCF-7 whole cell lysates, Lane 9: human A549 whole cell lysates, Lane 10: rat liver tissue lysates, Lane 11: rat PC-12 whole cell lysates, Lane 12: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUB1 antigen affinity purified polyclonal antibody (Catalog # A06089-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUB1 at approximately 75 kDa. The expected band size for NUB1 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06089-2-nub1-primary-antibodies-ihc-testing-2.jpgAnti-NUB1 Antibody Picoband® IHC analysis of NUB1 using anti-NUB1 antibody (A06089-2). NUB1 was detected in a paraffin-embedded section of human adrenal adenomas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUB1 Antibody (A06089-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06089-2-nub1-primary-antibodies-ihc-testing-3.jpgAnti-NUB1 Antibody Picoband® IHC analysis of NUB1 using anti-NUB1 antibody (A06089-2). NUB1 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUB1 Antibody (A06089-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06089-2-nub1-primary-antibodies-ihc-testing-4.jpgAnti-NUB1 Antibody Picoband® IHC analysis of NUB1 using anti-NUB1 antibody (A06089-2). NUB1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUB1 Antibody (A06089-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06089-2-nub1-primary-antibodies-if-testing-5.jpgAnti-NUB1 Antibody Picoband® IF analysis of NUB1 using anti-NUB1 antibody (A06089-2) and anti-Beta Tubulin antibody (M01857-3). NUB1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUB1 Antibody (A06089-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06089-2-nub1-primary-antibodies-fcm-testing-6.pngAnti-NUB1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-NUB1 antibody (A06089-2). Overlay histogram showing K562 cells stained with A06089-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUB1 Antibody (A06089-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nubp1-picoband-trade-antibody-a08538-1-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08538-1-nubp1-primary-antibodies-wb-testing-1.jpgAnti-NUBP1 Antibody Picoband® Western blot analysis of NUBP1 using anti-NUBP1 antibody (A08538-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: human Colo320 whole cell lysates, Lane 6: human HepG2 whole cell lysates, Lane 7: human U20S whole cell lysates, Lane 8: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUBP1 antigen affinity purified polyclonal antibody (Catalog # A08538-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUBP1 at approximately 35 kDa. The expected band size for NUBP1 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08538-1-nubp1-primary-antibodies-ihc-testing-1.jpgAnti-NUBP1 Antibody Picoband®IHC analysis of NUBP1 using anti-NUBP1 antibody (A08538-1). NUBP1 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUBP1 Antibody (A08538-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08538-1-nubp1-primary-antibodies-if-testing-2.jpgAnti-NUBP1 Antibody Picoband® IF analysis of NUBP1 using anti-NUBP1 antibody (A08538-1). NUBP1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUBP1 Antibody (A08538-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08538-1-nubp1-primary-antibodies-fcm-testing-3.pngAnti-NUBP1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-NUBP1 antibody (A08538-1). Overlay histogram showing K562 cells stained with A08538-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUBP1 Antibody (A08538-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nubpl-picoband-trade-antibody-a10634-1-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10634-1-nubpl-primary-antibodies-wb-testing-1_1.jpgAnti-NUBPL Antibody Picoband® Western blot analysis of NUBPL using anti-NUBPL antibody (A10634-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human T-47D whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: human Colo320 whole cell lysates, Lane 6: human MCF-7 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUBPL antigen affinity purified polyclonal antibody (Catalog # A10634-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUBPL at approximately 34 kDa. The expected band size for NUBPL is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10634-1-nubpl-primary-antibodies-ihc-testing-2_1.jpgAnti-NUBPL Antibody Picoband® IHC analysis of NUBPL using anti-NUBPL antibody (A10634-1). NUBPL was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUBPL Antibody (A10634-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10634-1-nubpl-primary-antibodies-ihc-testing-3_1.jpgAnti-NUBPL Antibody Picoband® IHC analysis of NUBPL using anti-NUBPL antibody (A10634-1). NUBPL was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUBPL Antibody (A10634-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10634-1-nubpl-primary-antibodies-ihc-testing-4_1.jpgAnti-NUBPL Antibody Picoband® IHC analysis of NUBPL using anti-NUBPL antibody (A10634-1). NUBPL was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUBPL Antibody (A10634-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10634-1-nubpl-primary-antibodies-if-testing-5_1.jpgAnti-NUBPL Antibody Picoband® IF analysis of NUBPL using anti-NUBPL antibody (A10634-1). NUBPL was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUBPL Antibody (A10634-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10634-1-nubpl-primary-antibodies-fcm-testing-6_1.pngAnti-NUBPL Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-NUBPL antibody (A10634-1). Overlay histogram showing MCF-7 cells stained with A10634-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUBPL Antibody (A10634-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nudcd1-picoband-trade-antibody-a10778-1-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10778-1-nudcd1-primary-antibodies-wb-testing-1.jpgAnti-NUDCD1 Antibody Picoband® Western blot analysis of NUDCD1 using anti-NUDCD1 antibody (A10778-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: human K562 whole cell lysates, Lane 6: human PC-3 whole cell lysates, Lane 7: human MCF-7 whole cell lysates, Lane 8: human U20S whole cell lysates, Lane 9: rat C6 whole cell lysates, Lane 10: monkey COS-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDCD1 antigen affinity purified polyclonal antibody (Catalog # A10778-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDCD1 at approximately 67 kDa. The expected band size for NUDCD1 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10778-1-nudcd1-primary-antibodies-ihc-testing-2.jpgAnti-NUDCD1 Antibody Picoband® IHC analysis of NUDCD1 using anti-NUDCD1 antibody (A10778-1). NUDCD1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDCD1 Antibody (A10778-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10778-1-nudcd1-primary-antibodies-ihc-testing-3.jpgAnti-NUDCD1 Antibody Picoband® IHC analysis of NUDCD1 using anti-NUDCD1 antibody (A10778-1). NUDCD1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDCD1 Antibody (A10778-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10778-1-nudcd1-primary-antibodies-if-testing-4.jpgAnti-NUDCD1 Antibody Picoband® IF analysis of NUDCD1 using anti-NUDCD1 antibody (A10778-1) and anti-Beta Tubulin antibody (M01857-3). NUDCD1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUDCD1 Antibody (A10778-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-maged4-picoband-trade-antibody-a16674-1-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16674-1-maged4-primary-antibodies-wb-testing-1.jpgAnti-MAGED4 Antibody Picoband® Western blot analysis of MAGED4 using anti-MAGED4 antibody (A16674-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAGED4 antigen affinity purified polyclonal antibody (Catalog # A16674-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAGED4 at approximately 100 kDa. The expected band size for MAGED4 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16674-1-maged4-primary-antibodies-ihc-testing-2.jpgAnti-MAGED4 Antibody Picoband® IHC analysis of MAGED4 using anti-MAGED4 antibody (A16674-1). MAGED4 was detected in a paraffin-embedded section of human adrenocortical adenoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAGED4 Antibody (A16674-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16674-1-maged4-primary-antibodies-ihc-testing-3.jpgAnti-MAGED4 Antibody Picoband® IHC analysis of MAGED4 using anti-MAGED4 antibody (A16674-1). MAGED4 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAGED4 Antibody (A16674-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16674-1-maged4-primary-antibodies-if-testing-4.jpgAnti-MAGED4 Antibody Picoband® IF analysis of MAGED4 using anti-MAGED4 antibody (A16674-1). MAGED4 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAGED4 Antibody (A16674-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16674-1-maged4-primary-antibodies-fcm-testing-5.pngAnti-MAGED4 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MAGED4 antibody (A16674-1). Overlay histogram showing HepG2 cells stained with A16674-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAGED4 Antibody (A16674-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mmp19-picoband-trade-antibody-a05171-3-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-3-mmp19-primary-antibodies-wb-testing-1.jpgAnti-MMP19 Antibody Picoband® Western blot analysis of MMP19 using anti-MMP19 antibody (A05171-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP19 antigen affinity purified polyclonal antibody (Catalog # A05171-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP19 at approximately 54 kDa. The expected band size for MMP19 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-3-mmp19-primary-antibodies-ihc-testing-2.jpgAnti-MMP19 Antibody Picoband® IHC analysis of MMP19 using anti-MMP19 antibody (A05171-3). MMP19 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MMP19 Antibody (A05171-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-3-mmp19-primary-antibodies-ihc-testing-3.jpgAnti-MMP19 Antibody Picoband® IHC analysis of MMP19 using anti-MMP19 antibody (A05171-3). MMP19 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MMP19 Antibody (A05171-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-3-mmp19-primary-antibodies-ihc-testing-4.jpgAnti-MMP19 Antibody Picoband® IHC analysis of MMP19 using anti-MMP19 antibody (A05171-3). MMP19 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MMP19 Antibody (A05171-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-3-mmp19-primary-antibodies-if-testing-5.jpgAnti-MMP19 Antibody Picoband® IF analysis of MMP19 using anti-MMP19 antibody (A05171-3). MMP19 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MMP19 Antibody (A05171-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05171-3-mmp19-primary-antibodies-fcm-testing-6.pngAnti-MMP19 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MMP19 antibody (A05171-3). Overlay histogram showing 293T cells stained with A05171-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MMP19 Antibody (A05171-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mnat1-picoband-trade-antibody-a06523-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06523-mnat1-primary-antibodies-wb-testing-1.jpgAnti-MNAT1 Antibody Picoband® Western blot analysis of MNAT1 using anti-MNAT1 antibody (A06523). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A375 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MNAT1 antigen affinity purified polyclonal antibody (Catalog # A06523) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MNAT1 at approximately 35 kDa. The expected band size for MNAT1 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06523-mnat1-primary-antibodies-if-testing-2.jpgAnti-MNAT1 Antibody Picoband® IF analysis of MNAT1 using anti-MNAT1 antibody (A06523) and anti-Beta Tubulin antibody (M01857-3). MNAT1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MNAT1 Antibody (A06523) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06523-mnat1-primary-antibodies-fcm-testing-3.pngAnti-MNAT1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MNAT1 antibody (A06523). Overlay histogram showing MCF-7 cells stained with A06523 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MNAT1 Antibody (A06523, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mnt-picoband-trade-antibody-a03357-4-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03357-4-mnt-primary-antibodies-wb-testing-1.jpgAnti-MNT Antibody Picoband® Western blot analysis of MNT using anti-MNT antibody (A03357-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MNT antigen affinity purified polyclonal antibody (Catalog # A03357-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MNT at approximately 62 kDa. The expected band size for MNT is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03357-4-mnt-primary-antibodies-if-testing-2.jpgAnti-MNT Antibody Picoband® IF analysis of MNT using anti-MNT antibody (A03357-4) and anti-Beta Tubulin antibody (M01857-3). MNT was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MNT Antibody (A03357-4) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-moap1-picoband-trade-antibody-a08043-1-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08043-1-moap1-primary-antibodies-wb-testing-1.jpgAnti-MOAP1 Antibody Picoband® Western blot analysis of MOAP1 using anti-MOAP1 antibody (A08043-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOAP1 antigen affinity purified polyclonal antibody (Catalog # A08043-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOAP1 at approximately 35 kDa. The expected band size for MOAP1 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08043-1-moap1-primary-antibodies-ihc-testing-2.jpgAnti-MOAP1 Antibody Picoband® IHC analysis of MOAP1 using anti-MOAP1 antibody (A08043-1). MOAP1 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOAP1 Antibody (A08043-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08043-1-moap1-primary-antibodies-ihc-testing-3.jpgAnti-MOAP1 Antibody Picoband® IHC analysis of MOAP1 using anti-MOAP1 antibody (A08043-1). MOAP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOAP1 Antibody (A08043-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08043-1-moap1-primary-antibodies-fcm-testing-4.pngAnti-MOAP1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-MOAP1 antibody (A08043-1). Overlay histogram showing U251 cells stained with A08043-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOAP1 Antibody (A08043-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mocs1-picoband-trade-antibody-a07628-1-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-1-mocs1-primary-antibodies-wb-testing-1.jpgAnti-MOCS1 Antibody Picoband® Western blot analysis of MOCS1 using anti-MOCS1 antibody (A07628-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human U20S whole cell lysates, Lane 6: human 293T whole cell lysates, Lane 7: human SH-SY5Y whole cell lysates, Lane 8: human RT4 whole cell lysates, Lane 9: rat liver tissue lysates, Lane 10: rat PC-12 whole cell lysates, Lane 11: mouse liver tissue lysates, Lane 12: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOCS1 antigen affinity purified polyclonal antibody (Catalog # A07628-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOCS1 at approximately 58 kDa. The expected band size for MOCS1 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-1-mocs1-primary-antibodies-ihc-testing-2.jpgAnti-MOCS1 Antibody Picoband® IHC analysis of MOCS1 using anti-MOCS1 antibody (A07628-1). MOCS1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS1 Antibody (A07628-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-1-mocs1-primary-antibodies-ihc-testing-3.jpgAnti-MOCS1 Antibody Picoband® IHC analysis of MOCS1 using anti-MOCS1 antibody (A07628-1). MOCS1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS1 Antibody (A07628-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-1-mocs1-primary-antibodies-ihc-testing-4.jpgAnti-MOCS1 Antibody Picoband® IHC analysis of MOCS1 using anti-MOCS1 antibody (A07628-1). MOCS1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS1 Antibody (A07628-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-1-mocs1-primary-antibodies-ihc-testing-5.jpgAnti-MOCS1 Antibody Picoband® IHC analysis of MOCS1 using anti-MOCS1 antibody (A07628-1). MOCS1 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS1 Antibody (A07628-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-1-mocs1-primary-antibodies-if-testing-6.jpgAnti-MOCS1 Antibody Picoband® IF analysis of MOCS1 using anti-MOCS1 antibody (A07628-1). MOCS1 was detected in an immunocytochemical section of HepG2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MOCS1 Antibody (A07628-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-1-mocs1-primary-antibodies-fcm-testing-7.pngAnti-MOCS1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-MOCS1 antibody (A07628-1). Overlay histogram showing K562 cells stained with A07628-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOCS1 Antibody (A07628-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rab7a-picoband-trade-antibody-a02409-2-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02409-2-rab7a-primary-antibodies-wb-testing-1.jpgAnti-RAB7A Antibody Picoband® Western blot analysis of RAB7A using anti-RAB7A antibody (A02409-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U87 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat L6 whole cell lysates, Lane 4: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB7A antigen affinity purified polyclonal antibody (Catalog # A02409-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAB7A at approximately 23 kDa. The expected band size for RAB7A is at 23 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nucks1-picoband-trade-antibody-a04997-3-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-wb-testing-1.jpgAnti-NUCKS1 Antibody Picoband® Western blot analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUCKS1 antigen affinity purified polyclonal antibody (Catalog # A04997-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUCKS1 at approximately 20 kDa. The expected band size for NUCKS1 is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-ihc-testing-2.jpgAnti-NUCKS1 Antibody Picoband® IHC analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-ihc-testing-3.jpgAnti-NUCKS1 Antibody Picoband® IHC analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-ihc-testing-4.jpgAnti-NUCKS1 Antibody Picoband® IHC analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-ihc-testing-5.jpgAnti-NUCKS1 Antibody Picoband® IHC analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-ihc-testing-6.jpgAnti-NUCKS1 Antibody Picoband® IHC analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-ihc-testing-7.jpgAnti-NUCKS1 Antibody Picoband® IHC analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-if-testing-8.jpgAnti-NUCKS1 Antibody Picoband® IF analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-if-testing-9.jpgAnti-NUCKS1 Antibody Picoband® IF analysis of NUCKS1 using anti-NUCKS1 antibody (A04997-3). NUCKS1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NUCKS1 Antibody (A04997-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04997-3-nucks1-primary-antibodies-fcm-testing-10.pngAnti-NUCKS1 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-NUCKS1 antibody (A04997-3). Overlay histogram showing Hela cells stained with A04997-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUCKS1 Antibody (A04997-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mphosph9-picoband-trade-antibody-a11350-2-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11350-2-mphosph9-primary-antibodies-wb-testing-1.jpgAnti-MPHOSPH9 Antibody Picoband® Western blot analysis of MPHOSPH9 using anti-MPHOSPH9 antibody (A11350-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPHOSPH9 antigen affinity purified polyclonal antibody (Catalog # A11350-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MPHOSPH9 at approximately 130-140 kDa. The expected band size for MPHOSPH9 is at 130-140 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11350-2-mphosph9-primary-antibodies-if-testing-2.jpgAnti-MPHOSPH9 Antibody Picoband® IF analysis of MPHOSPH9 using anti-MPHOSPH9 antibody (A11350-2). MPHOSPH9 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MPHOSPH9 Antibody (A11350-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11350-2-mphosph9-primary-antibodies-fcm-testing-3.pngAnti-MPHOSPH9 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-MPHOSPH9 antibody (A11350-2). Overlay histogram showing HEL cells stained with A11350-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MPHOSPH9 Antibody (A11350-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mphosph10-picoband-trade-antibody-a11510-3-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11510-3-mphosph10-primary-antibodies-wb-testing-1.jpgAnti-MPHOSPH10 Antibody Picoband® Western blot analysis of MPHOSPH10 using anti-MPHOSPH10 antibody (A11510-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPHOSPH10 antigen affinity purified polyclonal antibody (Catalog # A11510-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MPHOSPH10 at approximately 120 kDa. The expected band size for MPHOSPH10 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11510-3-mphosph10-primary-antibodies-if-testing-2.jpgAnti-MPHOSPH10 Antibody Picoband® IF analysis of MPHOSPH10 using anti-MPHOSPH10 antibody (A11510-3) and anti-Beta Tubulin antibody (M01857-3). MPHOSPH10 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MPHOSPH10 Antibody (A11510-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11510-3-mphosph10-primary-antibodies-fcm-testing-3.pngAnti-MPHOSPH10 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MPHOSPH10 antibody (A11510-3). Overlay histogram showing HepG2 cells stained with A11510-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MPHOSPH10 Antibody (A11510-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rsph3-picoband-trade-antibody-a11829-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11829-rsph3-primary-antibodies-wb-testing-1.jpgAnti-RSPH3 Antibody Picoband® Western blot analysis of RSPH3 using anti-RSPH3 antibody (A11829). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Siha whole cell lysates, Lane 2: human U87 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RSPH3 antigen affinity purified polyclonal antibody (Catalog # A11829) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RSPH3 at approximately 70 kDa. The expected band size for RSPH3 is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11829-rsph3-primary-antibodies-ihc-testing-2.jpgAnti-RSPH3 Antibody Picoband® IHC analysis of RSPH3 using anti-RSPH3 antibody (A11829). RSPH3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSPH3 Antibody (A11829) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11829-rsph3-primary-antibodies-if-testing-3.jpgAnti-RSPH3 Antibody Picoband® IF analysis of RSPH3 using anti-RSPH3 antibody (A11829). RSPH3 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RSPH3 Antibody (A11829) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11829-rsph3-primary-antibodies-fcm-testing-4.pngAnti-RSPH3 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-RSPH3 antibody (A11829). Overlay histogram showing K562 cells stained with A11829 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RSPH3 Antibody (A11829, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-melan-a-mlana-picoband-trade-antibody-a02033-3-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02033-3-mlana-primary-antibodies-wb-testing-1.jpgAnti-Melan-A/MLANA Antibody Picoband® Western blot analysis of Melan-A/MLANA using anti-Melan-A/MLANA antibody (A02033-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Melan-A/MLANA antigen affinity purified polyclonal antibody (Catalog # A02033-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Melan-A/MLANA at approximately 13 kDa. The expected band size for Melan-A/MLANA is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02033-3-mlana-primary-antibodies-fcm-testing-2.pngAnti-Melan-A/MLANA Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-Melan-A/MLANA antibody (A02033-3). Overlay histogram showing HEL cells stained with A02033-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Melan-A/MLANA Antibody (A02033-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-megf9-picoband-trade-antibody-a15544-2-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15544-2-megf9-primary-antibodies-wb-testing-1.jpgAnti-MEGF9 Antibody Picoband® Western blot analysis of MEGF9 using anti-MEGF9 antibody (A15544-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEGF9 antigen affinity purified polyclonal antibody (Catalog # A15544-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MEGF9 at approximately 63 kDa. The expected band size for MEGF9 is at 63 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-metap1d-picoband-trade-antibody-a11898-1-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11898-1-metap1d-primary-antibodies-wb-testing-1.jpgAnti-METAP1D Antibody Picoband® Western blot analysis of METAP1D using anti-METAP1D antibody (A11898-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: human THP-1 whole cell lysates, Lane 6: human Hela whole cell lysates, Lane 7: rat liver tissue lysates, Lane 8: rat RH35 whole cell lysates, Lane 9: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METAP1D antigen affinity purified polyclonal antibody (Catalog # A11898-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METAP1D at approximately 37 kDa. The expected band size for METAP1D is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11898-1-metap1d-primary-antibodies-ihc-testing-2.jpgAnti-METAP1D Antibody Picoband® IHC analysis of METAP1D using anti-METAP1D antibody (A11898-1). METAP1D was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METAP1D Antibody (A11898-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-metap2-picoband-trade-antibody-a03648-2-boster.html2026-03-17T05:15:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03648-2-metap2-primary-antibodies-wb-testing-1.jpgAnti-METAP2 Antibody Picoband® Western blot analysis of METAP2 using anti-METAP2 antibody (A03648-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: human DLD-1 whole cell lysates, Lane 6: human HT1080 whole cell lysates, Lane 7: human HL-60 whole cell lysates, Lane 8: monkey COS-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METAP2 antigen affinity purified polyclonal antibody (Catalog # A03648-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METAP2 at approximately 67 kDa. The expected band size for METAP2 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03648-2-metap2-primary-antibodies-wb-testing-2.jpgAnti-METAP2 Antibody Picoband® Western blot analysis of METAP2 using anti-METAP2 antibody (A03648-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat pancrease tissue lysates, Lane 2: rat testis tissue lysates, Lane 3: rat brain tissue lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse pancrease tissue lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse L929 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METAP2 antigen affinity purified polyclonal antibody (Catalog # A03648-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METAP2 at approximately 67 kDa. The expected band size for METAP2 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03648-2-metap2-primary-antibodies-ihc-testing-3.jpgAnti-METAP2 Antibody Picoband® IHC analysis of METAP2 using anti-METAP2 antibody (A03648-2). METAP2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METAP2 Antibody (A03648-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03648-2-metap2-primary-antibodies-ihc-testing-4.jpgAnti-METAP2 Antibody Picoband® IHC analysis of METAP2 using anti-METAP2 antibody (A03648-2). METAP2 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METAP2 Antibody (A03648-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03648-2-metap2-primary-antibodies-ihc-testing-5.jpgAnti-METAP2 Antibody Picoband® IHC analysis of METAP2 using anti-METAP2 antibody (A03648-2). METAP2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METAP2 Antibody (A03648-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-med29-picoband-trade-antibody-a10590-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10590-1-med29-primary-antibodies-wb-testing-1.jpgAnti-MED29 Antibody Picoband® Western blot analysis of MED29 using anti-MED29 antibody (A10590-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Siha whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: human Jurkat whole cell lysates, Lane 6: human U251 whole cell lysates, Lane 7: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED29 antigen affinity purified polyclonal antibody (Catalog # A10590-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED29 at approximately 21 kDa. The expected band size for MED29 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10590-1-med29-primary-antibodies-if-testing-2.jpgAnti-MED29 Antibody Picoband® IF analysis of MED29 using anti-MED29 antibody (A10590-1) and anti-Beta Tubulin antibody (M01857-3). MED29 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MED29 Antibody (A10590-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-mfap1-picoband-trade-antibody-a09850-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09850-1-mfap1-primary-antibodies-wb-testing-1.jpgAnti-MFAP1 Antibody Picoband® Western blot analysis of MFAP1 using anti-MFAP1 antibody (A09850-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MFAP1 antigen affinity purified polyclonal antibody (Catalog # A09850-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MFAP1 at approximately 50 kDa. The expected band size for MFAP1 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09850-1-mfap1-primary-antibodies-if-testing-2.jpgAnti-MFAP1 Antibody Picoband® IF analysis of MFAP1 using anti-MFAP1 antibody (A09850-1) and anti-Beta Tubulin antibody (M01857-3). MFAP1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MFAP1 Antibody (A09850-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09850-1-mfap1-primary-antibodies-fcm-testing-3.pngAnti-MFAP1 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-MFAP1 antibody (A09850-1). Overlay histogram showing A431 cells stained with A09850-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MFAP1 Antibody (A09850-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mfsd13a-picoband-trade-antibody-a17995-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17995-1-mfsd13a-primary-antibodies-wb-testing-1.jpgAnti-MFSD13A Antibody Picoband® Western blot analysis of MFSD13A using anti-MFSD13A antibody (A17995-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: human K562 whole cell lysates, Lane 6: human A431 whole cell lysates, Lane 7: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MFSD13A antigen affinity purified polyclonal antibody (Catalog # A17995-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MFSD13A at approximately 57 kDa. The expected band size for MFSD13A is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17995-1-mfsd13a-primary-antibodies-fcm-testing-2.pngAnti-MFSD13A Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MFSD13A antibody (A17995-1). Overlay histogram showing JK cells stained with A17995-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MFSD13A Antibody (A17995-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mis12-picoband-trade-antibody-a06832-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06832-1-mis12-primary-antibodies-wb-testing-1.jpgAnti-MIS12 Antibody Picoband® Western blot analysis of MIS12 using anti-MIS12 antibody (A06832-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: human Hacat whole cell lysates, Lane 6: human U251 whole cell lysates, Lane 7: human SH-SY5Y whole cell lysates, Lane 8: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIS12 antigen affinity purified polyclonal antibody (Catalog # A06832-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIS12 at approximately 25 kDa. The expected band size for MIS12 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06832-1-mis12-primary-antibodies-if-testing-2.jpgAnti-MIS12 Antibody Picoband® IF analysis of MIS12 using anti-MIS12 antibody (A06832-1). MIS12 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MIS12 Antibody (A06832-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06832-1-mis12-primary-antibodies-fcm-testing-3.pngAnti-MIS12 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MIS12 antibody (A06832-1). Overlay histogram showing JK cells stained with A06832-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MIS12 Antibody (A06832-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-c21orf45-mis18a-picoband-trade-antibody-a10791-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10791-1-mis18a-primary-antibodies-wb-testing-1.jpgAnti-C21orf45/MIS18A Antibody Picoband® Western blot analysis of C21orf45/MIS18A using anti-C21orf45/MIS18A antibody (A10791-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C21orf45/MIS18A antigen affinity purified polyclonal antibody (Catalog # A10791-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C21orf45/MIS18A at approximately 26 kDa. The expected band size for C21orf45/MIS18A is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10791-1-mis18a-primary-antibodies-if-testing-2.jpgAnti-C21orf45/MIS18A Antibody Picoband® IF analysis of C21orf45/MIS18A using anti-C21orf45/MIS18A antibody (A10791-1) and anti-Beta Tubulin antibody (M01857-3). C21orf45/MIS18A was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-C21orf45/MIS18A Antibody (A10791-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10791-1-mis18a-primary-antibodies-fcm-testing-3.pngAnti-C21orf45/MIS18A Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-C21orf45/MIS18A antibody (A10791-1). Overlay histogram showing HEL cells stained with A10791-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-C21orf45/MIS18A Antibody (A10791-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-misp-picoband-trade-antibody-a08017-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08017-1-misp-primary-antibodies-wb-testing-1.jpgAnti-MISP Antibody Picoband® Western blot analysis of MISP using anti-MISP antibody (A08017-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MISP antigen affinity purified polyclonal antibody (Catalog # A08017-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MISP at approximately 75 kDa. The expected band size for MISP is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08017-1-misp-primary-antibodies-if-testing-2.jpgAnti-MISP Antibody Picoband® IF analysis of MISP using anti-MISP antibody (A08017-1). MISP was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MISP Antibody (A08017-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08017-1-misp-primary-antibodies-fcm-testing-3.pngAnti-MISP Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-MISP antibody (A08017-1). Overlay histogram showing Caco-2 cells stained with A08017-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MISP Antibody (A08017-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-prr9-picoband-trade-antibody-a14833-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14833-prr9-primary-antibodies-wb-testing-1.jpgAnti-PRR9 Antibody Picoband® Western blot analysis of PRR9 using anti-PRR9 antibody (A14833). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRR9 antigen affinity purified polyclonal antibody (Catalog # A14833) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRR9 at approximately 13 kDa. The expected band size for PRR9 is at 13 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-nap1l1-picoband-trade-antibody-a05100-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05100-1-nap1l1-primary-antibodies-wb-testing-1.jpgAnti-NAP1L1 Antibody Picoband® Western blot analysis of NAP1L1 using anti-NAP1L1 antibody (A05100-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat thymus tissue lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse thymus tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAP1L1 antigen affinity purified polyclonal antibody (Catalog # A05100-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAP1L1 at approximately 55 kDa. The expected band size for NAP1L1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05100-1-nap1l1-primary-antibodies-if-testing-2.jpgAnti-NAP1L1 Antibody Picoband® IF analysis of NAP1L1 using anti-NAP1L1 antibody (A05100-1). NAP1L1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NAP1L1 Antibody (A05100-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05100-1-nap1l1-primary-antibodies-fcm-testing-3.pngAnti-NAP1L1 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-NAP1L1 antibody (A05100-1). Overlay histogram showing PC-3 cells stained with A05100-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAP1L1 Antibody (A05100-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nap1l5-picoband-trade-antibody-a14492-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14492-1-nap1l5-primary-antibodies-wb-testing-1.jpgAnti-NAP1L5 Antibody Picoband® Western blot analysis of NAP1L5 using anti-NAP1L5 antibody (A14492-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse EL-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAP1L5 antigen affinity purified polyclonal antibody (Catalog # A14492-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAP1L5 at approximately 19 kDa. The expected band size for NAP1L5 is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14492-1-nap1l5-primary-antibodies-if-testing-2.jpgAnti-NAP1L5 Antibody Picoband® IF analysis of NAP1L5 using anti-NAP1L5 antibody (A14492-1) and anti-Beta Tubulin antibody (M01857-3). NAP1L5 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NAP1L5 Antibody (A14492-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14492-1-nap1l5-primary-antibodies-fcm-testing-3.pngAnti-NAP1L5 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-NAP1L5 antibody (A14492-1). Overlay histogram showing Hela cells stained with A14492-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAP1L5 Antibody (A14492-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-alpha-snap-napa-picoband-trade-antibody-a05153-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05153-1-napa-primary-antibodies-wb-testing-1.jpgAnti-Alpha SNAP/NAPA Antibody Picoband® Western blot analysis of Alpha SNAP/NAPA using anti-Alpha SNAP/NAPA antibody (A05153-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human THP-1 whole cell lysates, Lane 6: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha SNAP/NAPA antigen affinity purified polyclonal antibody (Catalog # A05153-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Alpha SNAP/NAPA at approximately 33 kDa. The expected band size for Alpha SNAP/NAPA is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05153-1-napa-primary-antibodies-fcm-testing-2.pngAnti-Alpha SNAP/NAPA Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-Alpha SNAP/NAPA antibody (A05153-1). Overlay histogram showing 293T cells stained with A05153-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Alpha SNAP/NAPA Antibody (A05153-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-napb-picoband-trade-antibody-a00939-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00939-1-napb-primary-antibodies-wb-testing-1.jpgAnti-NAPB Antibody Picoband® Western blot analysis of NAPB using anti-NAPB antibody (A00939-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAPB antigen affinity purified polyclonal antibody (Catalog # A00939-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAPB at approximately 35 kDa. The expected band size for NAPB is at 34 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-hbegf-picoband-trade-antibody-a01759-4-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01759-4-hbegf-primary-antibodies-wb-testing-1.jpgAnti-Hbegf Antibody Picoband® Western blot analysis of Hbegf using anti-Hbegf antibody (A01759-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hbegf antigen affinity purified polyclonal antibody (Catalog # A01759-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hbegf at approximately 20 kDa. The expected band size for Hbegf is at 23 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-mindy3-picoband-trade-antibody-a32140-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32140-1-mindy3-primary-antibodies-wb-testing-1.jpgAnti-MINDY3 Antibody Picoband® Western blot analysis of MINDY3 using anti-MINDY3 antibody (A32140-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: monkey COS-7 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human SH-SY5Y whole cell lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MINDY3 antigen affinity purified polyclonal antibody (Catalog # A32140-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MINDY3 at approximately 50 kDa. The expected band size for MINDY3 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32140-1-mindy3-primary-antibodies-if-testing-2.jpgAnti-MINDY3 Antibody Picoband® IF analysis of MINDY3 using anti-MINDY3 antibody (A32140-1). MINDY3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MINDY3 Antibody (A32140-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32140-1-mindy3-primary-antibodies-fcm-testing-3.pngAnti-MINDY3 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MINDY3 antibody (A32140-1). Overlay histogram showing Hela cells stained with A32140-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MINDY3 Antibody (A32140-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mmachc-picoband-trade-antibody-a03398-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03398-1-mmachc-primary-antibodies-wb-testing-1.jpgAnti-MMACHC Antibody Picoband® Western blot analysis of MMACHC using anti-MMACHC antibody (A03398-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMACHC antigen affinity purified polyclonal antibody (Catalog # A03398-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMACHC at approximately 32 kDa. The expected band size for MMACHC is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03398-1-mmachc-primary-antibodies-fcm-testing-2.pngAnti-MMACHC Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MMACHC antibody (A03398-1). Overlay histogram showing JK cells stained with A03398-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MMACHC Antibody (A03398-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mms19-picoband-trade-antibody-a06218-2-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06218-2-mms19-primary-antibodies-wb-testing-1.jpgAnti-MMS19 Antibody Picoband® Western blot analysis of MMS19 using anti-MMS19 antibody (A06218-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMS19 antigen affinity purified polyclonal antibody (Catalog # A06218-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMS19 at approximately 113 kDa. The expected band size for MMS19 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06218-2-mms19-primary-antibodies-ihc-testing-2.jpgAnti-MMS19 Antibody Picoband® IHC analysis of MMS19 using anti-MMS19 antibody (A06218-2). MMS19 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MMS19 Antibody (A06218-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06218-2-mms19-primary-antibodies-ihc-testing-3.jpgAnti-MMS19 Antibody Picoband® IHC analysis of MMS19 using anti-MMS19 antibody (A06218-2). MMS19 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MMS19 Antibody (A06218-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06218-2-mms19-primary-antibodies-ihc-testing-4.jpgAnti-MMS19 Antibody Picoband® IHC analysis of MMS19 using anti-MMS19 antibody (A06218-2). MMS19 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MMS19 Antibody (A06218-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06218-2-mms19-primary-antibodies-if-testing-5.jpgAnti-MMS19 Antibody Picoband® IF analysis of MMS19 using anti-MMS19 antibody (A06218-2). MMS19 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MMS19 Antibody (A06218-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06218-2-mms19-primary-antibodies-fcm-testing-6.pngAnti-MMS19 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MMS19 antibody (A06218-2). Overlay histogram showing Hela cells stained with A06218-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MMS19 Antibody (A06218-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mocs2-picoband-trade-antibody-a07401-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07401-mocs2-primary-antibodies-wb-testing-1.jpgAnti-MOCS2 Antibody Picoband® Western blot analysis of MOCS2 using anti-MOCS2 antibody (A07401). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human LNCAP whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: human Jurkat whole cell lysates, Lane 6: human K562 whole cell lysates, Lane 7: human HepG2 whole cell lysates, Lane 8: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOCS2 antigen affinity purified polyclonal antibody (Catalog # A07401) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOCS2 at approximately 21 kDa. The expected band size for MOCS2 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07401-mocs2-primary-antibodies-ihc-testing-2.jpgAnti-MOCS2 Antibody Picoband® IHC analysis of MOCS2 using anti-MOCS2 antibody (A07401). MOCS2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS2 Antibody (A07401) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07401-mocs2-primary-antibodies-ihc-testing-3.jpgAnti-MOCS2 Antibody Picoband® IHC analysis of MOCS2 using anti-MOCS2 antibody (A07401). MOCS2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS2 Antibody (A07401) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07401-mocs2-primary-antibodies-ihc-testing-4.jpgAnti-MOCS2 Antibody Picoband® IHC analysis of MOCS2 using anti-MOCS2 antibody (A07401). MOCS2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS2 Antibody (A07401) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07401-mocs2-primary-antibodies-ihc-testing-5.jpgAnti-MOCS2 Antibody Picoband® IHC analysis of MOCS2 using anti-MOCS2 antibody (A07401). MOCS2 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOCS2 Antibody (A07401) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07401-mocs2-primary-antibodies-fcm-testing-6.pngAnti-MOCS2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MOCS2 antibody (A07401). Overlay histogram showing JK cells stained with A07401 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOCS2 Antibody (A07401, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mpzl1-picoband-trade-antibody-a06667-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06667-1-mpzl1-primary-antibodies-wb-testing-1.jpgAnti-MPZL1 Antibody Picoband® Western blot analysis of MPZL1 using anti-MPZL1 antibody (A06667-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPZL1 antigen affinity purified polyclonal antibody (Catalog # A06667-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MPZL1 at approximately 29-37 kDa. The expected band size for MPZL1 is at 29 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-msrb3-picoband-trade-antibody-a06632-1-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06632-1-msrb3-primary-antibodies-wb-testing-1.jpgAnti-MSRB3 Antibody Picoband® Western blot analysis of MSRB3 using anti-MSRB3 antibody (A06632-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MSRB3 antigen affinity purified polyclonal antibody (Catalog # A06632-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MSRB3 at approximately 21 kDa. The expected band size for MSRB3 is at 21 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-mycbp-picoband-trade-antibody-a06216-2-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06216-2-mycbp-primary-antibodies-wb-testing-1_1.jpgAnti-MYCBP Antibody Picoband® Western blot analysis of MYCBP using anti-MYCBP antibody (A06216-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates; Lane 3: rat lung tissue lysates; Lane 4: rat NRK whole cell lysates; Lane 5: mouse lung tissue lysates; Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYCBP antigen affinity purified polyclonal antibody (Catalog # A06216-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYCBP at approximately 12 kDa. The expected band size for MYCBP is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06216-2-mycbp-primary-antibodies-ihc-testing-2.jpgAnti-MYCBP Antibody Picoband® IHC analysis of MYCBP using anti-MYCBP antibody (A06216-2). MYCBP was detected in a paraffin-embedded section of human adrenal adenomas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYCBP Antibody (A06216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06216-2-mycbp-primary-antibodies-ihc-testing-3.jpgAnti-MYCBP Antibody Picoband® IHC analysis of MYCBP using anti-MYCBP antibody (A06216-2). MYCBP was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYCBP Antibody (A06216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06216-2-mycbp-primary-antibodies-ihc-testing-4.jpgAnti-MYCBP Antibody Picoband® IHC analysis of MYCBP using anti-MYCBP antibody (A06216-2). MYCBP was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYCBP Antibody (A06216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06216-2-mycbp-primary-antibodies-ihc-testing-5.jpgAnti-MYCBP Antibody Picoband® IHC analysis of MYCBP using anti-MYCBP antibody (A06216-2). MYCBP was detected in a paraffin-embedded section of human testicular germ cell tumors. tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYCBP Antibody (A06216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06216-2-mycbp-primary-antibodies-fcm-testing-6.pngAnti-MYCBP Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-MYCBP antibody (A06216-2). Overlay histogram showing PC-3 cells stained with A06216-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYCBP Antibody (A06216-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-c19orf10-mydgf-picoband-trade-antibody-a08602-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-wb-testing-1.jpgAnti-C19orf10/MYDGF Antibody Picoband® Western blot analysis of C19orf10/MYDGF using anti-C19orf10/MYDGF antibody (A08602). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: human U251 whole cell lysates, Lane 6: human THP-1 whole cell lysates, Lane 7: human A431 whole cell lysates, Lane 8: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C19orf10/MYDGF antigen affinity purified polyclonal antibody (Catalog # A08602) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C19orf10/MYDGF at approximately 15 kDa. The expected band size for C19orf10/MYDGF is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-wb-testing-2.jpgAnti-C19orf10/MYDGF Antibody Picoband® Western blot analysis of C19orf10/MYDGF using anti-C19orf10/MYDGF antibody (A08602). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat NRK whole cell lysates, Lane 3: mouse ovary tissue lysates, Lane 4: mouse stomach tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C19orf10/MYDGF antigen affinity purified polyclonal antibody (Catalog # A08602) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C19orf10/MYDGF at approximately 15 kDa. The expected band size for C19orf10/MYDGF is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-ihc-testing-3.jpgAnti-C19orf10/MYDGF Antibody Picoband® IHC analysis of C19orf10/MYDGF using anti-C19orf10/MYDGF antibody (A08602). C19orf10/MYDGF was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C19orf10/MYDGF Antibody (A08602) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-ihc-testing-4.jpgAnti-C19orf10/MYDGF Antibody Picoband® IHC analysis of C19orf10/MYDGF using anti-C19orf10/MYDGF antibody (A08602). C19orf10/MYDGF was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C19orf10/MYDGF Antibody (A08602) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-ihc-testing-5.jpgAnti-C19orf10/MYDGF Antibody Picoband® IHC analysis of C19orf10/MYDGF using anti-C19orf10/MYDGF antibody (A08602). C19orf10/MYDGF was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C19orf10/MYDGF Antibody (A08602) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-ihc-testing-6.jpgAnti-C19orf10/MYDGF Antibody Picoband® IHC analysis of C19orf10/MYDGF using anti-C19orf10/MYDGF antibody (A08602). C19orf10/MYDGF was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C19orf10/MYDGF Antibody (A08602) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-ihc-testing-7.jpgAnti-C19orf10/MYDGF Antibody Picoband® IHC analysis of C19orf10/MYDGF using anti-C19orf10/MYDGF antibody (A08602). C19orf10/MYDGF was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C19orf10/MYDGF Antibody (A08602) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08602-mydgf-primary-antibodies-fcm-testing-8.pngAnti-C19orf10/MYDGF Antibody Picoband® Flow Cytometry analysis of JK cells using anti-C19orf10/MYDGF antibody (A08602). Overlay histogram showing JK cells stained with A08602 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-C19orf10/MYDGF Antibody (A08602, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-myh16-picoband-trade-antibody-a15498-boster.html2026-03-17T05:15:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15498-myh16-primary-antibodies-wb-testing-1.jpgAnti-MYH16 Antibody Picoband® Western blot analysis of MYH16 using anti-MYH16 antibody (A15498). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYH16 antigen affinity purified polyclonal antibody (Catalog # A15498) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYH16 at approximately 128 kDa. The expected band size for MYH16 is at 128 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15498-myh16-primary-antibodies-if-testing-2.jpgAnti-MYH16 Antibody Picoband® IF analysis of MYH16 using anti-MYH16 antibody (A15498). MYH16 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MYH16 Antibody (A15498) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15498-myh16-primary-antibodies-fcm-testing-3.pngAnti-MYH16 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MYH16 antibody (A15498). Overlay histogram showing JK cells stained with A15498 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYH16 Antibody (A15498, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-myl5-picoband-trade-antibody-a15974-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15974-myl5-primary-antibodies-wb-testing-1.jpgAnti-MYL5 Antibody Picoband® Western blot analysis of MYL5 using anti-MYL5 antibody (A15974). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skeletal muscle tissue lysates, Lane 2: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYL5 antigen affinity purified polyclonal antibody (Catalog # A15974) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYL5 at approximately 18 kDa. The expected band size for MYL5 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15974-myl5-primary-antibodies-ihc-testing-2.jpgAnti-MYL5 Antibody Picoband® IHC analysis of MYL5 using anti-MYL5 antibody (A15974). MYL5 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYL5 Antibody (A15974) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15974-myl5-primary-antibodies-if-testing-3.jpgAnti-MYL5 Antibody Picoband® IF analysis of MYL5 using anti-MYL5 antibody (A15974). MYL5 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MYL5 Antibody (A15974) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15974-myl5-primary-antibodies-fcm-testing-4.pngAnti-MYL5 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MYL5 antibody (A15974). Overlay histogram showing JK cells stained with A15974 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYL5 Antibody (A15974, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mynn-picoband-trade-antibody-a12268-2-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12268-2-mynn-primary-antibodies-wb-testing-1.jpgAnti-MYNN Antibody Picoband® Western blot analysis of MYNN using anti-MYNN antibody (A12268-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Colo320 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYNN antigen affinity purified polyclonal antibody (Catalog # A12268-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYNN at approximately 69 kDa. The expected band size for MYNN is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12268-2-mynn-primary-antibodies-ihc-testing-2.jpgAnti-MYNN Antibody Picoband® IHC analysis of MYNN using anti-MYNN antibody (A12268-2). MYNN was detected in a paraffin-embedded section of human braest cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYNN Antibody (A12268-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12268-2-mynn-primary-antibodies-ihc-testing-3.jpgAnti-MYNN Antibody Picoband® IHC analysis of MYNN using anti-MYNN antibody (A12268-2). MYNN was detected in a paraffin-embedded section of human cervica squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYNN Antibody (A12268-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12268-2-mynn-primary-antibodies-ihc-testing-4.jpgAnti-MYNN Antibody Picoband® IHC analysis of MYNN using anti-MYNN antibody (A12268-2). MYNN was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYNN Antibody (A12268-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12268-2-mynn-primary-antibodies-if-testing-5.jpgAnti-MYNN Antibody Picoband® IF analysis of MYNN using anti-MYNN antibody (A12268-2) and anti-Beta Tubulin antibody (M01857-3). MYNN was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MYNN Antibody (A12268-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12268-2-mynn-primary-antibodies-fcm-testing-6.pngAnti-MYNN Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MYNN antibody (A12268-2). Overlay histogram showing 293T cells stained with A12268-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYNN Antibody (A12268-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-myo1b-picoband-trade-antibody-a07011-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07011-1-myo1b-primary-antibodies-wb-testing-1.jpgAnti-MYO1B Antibody Picoband® Western blot analysis of MYO1B using anti-MYO1B antibody (A07011-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYO1B antigen affinity purified polyclonal antibody (Catalog # A07011-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYO1B at approximately 124 kDa. The expected band size for MYO1B is at 132 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07011-1-myo1b-primary-antibodies-fcm-testing-2.pngAnti-MYO1B Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MYO1B antibody (A07011-1). Overlay histogram showing MCF-7 cells stained with A07011-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYO1B Antibody (A07011-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-myo6-picoband-trade-antibody-a02627-2-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02627-2-myo6-primary-antibodies-wb-testing-1.jpgAnti-MYO6 Antibody Picoband® Western blot analysis of MYO6 using anti-MYO6 antibody (A02627-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYO6 antigen affinity purified polyclonal antibody (Catalog # A02627-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYO6 at approximately 150 kDa. The expected band size for MYO6 is at 150 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02627-2-myo6-primary-antibodies-fcm-testing-2.pngAnti-MYO6 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MYO6 antibody (A02627-2). Overlay histogram showing Hela cells stained with A02627-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYO6 Antibody (A02627-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lhx6-picoband-trade-antibody-a07568-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07568-1-lhx6-primary-antibodies-wb-testing-1.jpgAnti-LHX6 Antibody Picoband® Western blot analysis of LHX6 using anti-LHX6 antibody (A07568-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LHX6 antigen affinity purified polyclonal antibody (Catalog # A07568-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LHX6 at approximately 60 kDa. The expected band size for LHX6 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07568-1-lhx6-primary-antibodies-ihc-testing-2.jpgAnti-LHX6 Antibody Picoband® IHC analysis of LHX6 using anti-LHX6 antibody (A07568-1). LHX6 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LHX6 Antibody (A07568-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07568-1-lhx6-primary-antibodies-if-testing-3.jpgAnti-LHX6 Antibody Picoband® IF analysis of LHX6 using anti-LHX6 antibody (A07568-1) and anti-Beta Tubulin antibody (M01857-3). LHX6 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LHX6 Antibody (A07568-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-eb1-mapre1-picoband-trade-antibody-a02070-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02070-1-mapre1-primary-antibodies-wb-testing-1.jpgAnti-EB1/MAPRE1 Antibody Picoband® Western blot analysis of EB1/MAPRE1 using anti-EB1/MAPRE1 antibody (A02070-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Ramos whole cell lysates, Lane 5: human 293T whole cell lysates, Lane 6: human Caco-2 whole cell lysates, Lane 7: human HEL whole cell lysates, Lane 8: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EB1/MAPRE1 antigen affinity purified polyclonal antibody (Catalog # A02070-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EB1/MAPRE1 at approximately 35 kDa. The expected band size for EB1/MAPRE1 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02070-1-mapre1-primary-antibodies-wb-testing-2.jpgAnti-EB1/MAPRE1 Antibody Picoband® Western blot analysis of EB1/MAPRE1 using anti-EB1/MAPRE1 antibody (A02070-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat lung tissue lysates, Lane 2: rat stomach tissue lysates, Lane 3: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EB1/MAPRE1 antigen affinity purified polyclonal antibody (Catalog # A02070-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EB1/MAPRE1 at approximately 35 kDa. The expected band size for EB1/MAPRE1 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02070-1-mapre1-primary-antibodies-fcm-testing-3.pngAnti-EB1/MAPRE1 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-MAPRE1 antibody (A02070-1). Overlay histogram showing SiHa cells stained with A02070-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAPRE1 Antibody (A02070-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-alpha-1-microglobulin-ambp-picoband-trade-antibody-a02419-4-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02419-4-ambp-primary-antibodies-wb-testing-1.jpgAnti-Alpha 1 microglobulin/Ambp Antibody Picoband® Western blot analysis of Alpha 1 Microglobulin/Ambp using anti-Alpha 1 Microglobulin/Ambp antibody (A02419-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse kidney tissue lysates, Lane 3: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha 1 Microglobulin/Ambp antigen affinity purified polyclonal antibody (Catalog # A02419-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Alpha 1 Microglobulin/Ambp at approximately 39 kDa. The expected band size for Alpha 1 Microglobulin/Ambp is at 39 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-vegfc-picoband-trade-antibody-a00623-3-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00623-3-vegfc-primary-antibodies-wb-testing-1.jpgAnti-Vegfc Antibody Picoband® Western blot analysis of Vegfc using anti-Vegfc antibody (A00623-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Vegfc antigen affinity purified polyclonal antibody (Catalog # A00623-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Vegfc at approximately 46 kDa. The expected band size for Vegfc is at 46 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-cbp20-ncbp2-picoband-trade-antibody-a08031-2-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08031-2-ncbp2-primary-antibodies-wb-testing-1.jpgAnti-CBP20/NCBP2 Antibody Picoband® Western blot analysis of CBP20/NCBP2 using anti-CBP20/NCBP2 antibody (A08031-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human CCRF-CEM whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CBP20/NCBP2 antigen affinity purified polyclonal antibody (Catalog # A08031-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CBP20/NCBP2 at approximately 18 kDa. The expected band size for CBP20/NCBP2 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08031-2-ncbp2-primary-antibodies-ihc-testing-2.jpgAnti-CBP20/NCBP2 Antibody Picoband® IHC analysis of CBP20/NCBP2 using anti-CBP20/NCBP2 antibody (A08031-2). CBP20/NCBP2 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CBP20/NCBP2 Antibody (A08031-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08031-2-ncbp2-primary-antibodies-ihc-testing-3.jpgAnti-CBP20/NCBP2 Antibody Picoband® IHC analysis of CBP20/NCBP2 using anti-CBP20/NCBP2 antibody (A08031-2). CBP20/NCBP2 was detected in a paraffin-embedded section of human adrenocortical adenoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CBP20/NCBP2 Antibody (A08031-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08031-2-ncbp2-primary-antibodies-if-testing-4.jpgAnti-CBP20/NCBP2 Antibody Picoband® IF analysis of CBP20/NCBP2 using anti-CBP20/NCBP2 antibody (A08031-2). CBP20/NCBP2 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CBP20/NCBP2 Antibody (A08031-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08031-2-ncbp2-primary-antibodies-fcm-testing-5.pngAnti-CBP20/NCBP2 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-CBP20/NCBP2 antibody (A08031-2). Overlay histogram showing U251 cells stained with A08031-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CBP20/NCBP2 Antibody (A08031-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-polr2b-picoband-trade-antibody-a08699-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08699-1-polr2b-primary-antibodies-wb-testing-1.jpgAnti-POLR2B Antibody Picoband® Western blot analysis of POLR2B using anti-POLR2B antibody (A08699-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Ramos whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLR2B antigen affinity purified polyclonal antibody (Catalog # A08699-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLR2B at approximately 130 kDa. The expected band size for POLR2B is at 134 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08699-1-polr2b-primary-antibodies-if-testing-2.jpgAnti-POLR2B Antibody Picoband® IF analysis of POLR2B using anti-POLR2B antibody (A08699-1) and anti-Beta Tubulin antibody (M01857-3). POLR2B was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POLR2B Antibody (A08699-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08699-1-polr2b-primary-antibodies-fcm-testing-3.pngAnti-POLR2B Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-POLR2B antibody (A08699-1). Overlay histogram showing U251 cells stained with A08699-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POLR2B Antibody (A08699-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-map6d1-picoband-trade-antibody-a15534-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15534-1-map6d1-primary-antibodies-wb-testing-1.jpgAnti-MAP6D1 Antibody Picoband® Western blot analysis of MAP6D1 using anti-MAP6D1 antibody (A15534-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human T-47D whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP6D1 antigen affinity purified polyclonal antibody (Catalog # A15534-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP6D1 at approximately 21 kDa. The expected band size for MAP6D1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15534-1-map6d1-primary-antibodies-ihc-testing-2.jpgAnti-MAP6D1 Antibody Picoband® IHC analysis of MAP6D1 using anti-MAP6D1 antibody (A15534-1). MAP6D1 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP6D1 Antibody (A15534-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15534-1-map6d1-primary-antibodies-ihc-testing-3.jpgAnti-MAP6D1 Antibody Picoband® IHC analysis of MAP6D1 using anti-MAP6D1 antibody (A15534-1). MAP6D1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP6D1 Antibody (A15534-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15534-1-map6d1-primary-antibodies-ihc-testing-4.jpgAnti-MAP6D1 Antibody Picoband® IHC analysis of MAP6D1 using anti-MAP6D1 antibody (A15534-1). MAP6D1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP6D1 Antibody (A15534-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15534-1-map6d1-primary-antibodies-fcm-testing-5.pngAnti-MAP6D1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-MAP6D1 antibody (A15534-1). Overlay histogram showing SH-SY5Y cells stained with A15534-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAP6D1 Antibody (A15534-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15534-1-map6d1-primary-antibodies-if-testing-6.jpgAnti-MAP6D1 Antibody Picoband® IF analysis of MAP6D1 using anti-MAP6D1 antibody (A15534-1). MAP6D1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAP6D1 Antibody (A15534-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15534-1-map6d1-primary-antibodies-if-testing-7.jpgAnti-MAP6D1 Antibody Picoband® IF analysis of MAP6D1 using anti-MAP6D1 antibody (A15534-1). MAP6D1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAP6D1 Antibody (A15534-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-l3mbtl3-picoband-trade-antibody-a10834-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10834-1-l3mbtl3-primary-antibodies-wb-testing-1.jpgAnti-L3MBTL3 Antibody Picoband® Western blot analysis of L3MBTL3 using anti-L3MBTL3 antibody (A10834-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-L3MBTL3 antigen affinity purified polyclonal antibody (Catalog # A10834-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for L3MBTL3 at approximately 90 kDa. The expected band size for L3MBTL3 is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10834-1-l3mbtl3-primary-antibodies-ihc-testing-2.jpgAnti-L3MBTL3 Antibody Picoband® IHC analysis of L3MBTL3 using anti-L3MBTL3 antibody (A10834-1). L3MBTL3 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-L3MBTL3 Antibody (A10834-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10834-1-l3mbtl3-primary-antibodies-fcm-testing-3.pngAnti-L3MBTL3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-L3MBTL3 antibody (A10834-1). Overlay histogram showing U251 cells stained with A10834-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-L3MBTL3 Antibody (A10834-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-malectin-mlec-picoband-trade-antibody-a10455-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-wb-testing-1.jpgAnti-Malectin/MLEC Antibody Picoband® Western blot analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: human A431 whole cell lysates, Lane 6: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Malectin/MLEC antigen affinity purified polyclonal antibody (Catalog # A10455-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Malectin/MLEC at approximately 32 kDa. The expected band size for Malectin/MLEC is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-wb-testing-2.jpgAnti-Malectin/MLEC Antibody Picoband® Western blot analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates, Lane 3: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Malectin/MLEC antigen affinity purified polyclonal antibody (Catalog # A10455-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Malectin/MLEC at approximately 32 kDa. The expected band size for Malectin/MLEC is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-3.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-4.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-5.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-6.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-7.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-8.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-9.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-ihc-testing-10.jpgAnti-Malectin/MLEC Antibody Picoband® IHC analysis of Malectin/MLEC using anti-Malectin/MLEC antibody (A10455-1). Malectin/MLEC was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Malectin/MLEC Antibody (A10455-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10455-1-mlec-primary-antibodies-fcm-testing-11.pngAnti-Malectin/MLEC Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Malectin/MLEC antibody (A10455-1). Overlay histogram showing SiHa cells stained with A10455-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Malectin/MLEC Antibody (A10455-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mesothelin-msln-picoband-trade-antibody-a03266-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03266-1-msln-primary-antibodies-wb-testing-1.jpgAnti-Mesothelin/Msln Antibody Picoband® Western blot analysis of Mesothelin/Msln using anti-Mesothelin/Msln antibody (A03266-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Mesothelin/Msln antigen affinity purified polyclonal antibody (Catalog # A03266-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Mesothelin/Msln at approximately 69 kDa. The expected band size for Mesothelin/Msln is at 69 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-mslnl-picoband-trade-antibody-a17693-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17693-mslnl-primary-antibodies-wb-testing-1.jpgAnti-MSLNL Antibody Picoband® Western blot analysis of MSLNL using anti-MSLNL antibody (A17693). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MSLNL antigen affinity purified polyclonal antibody (Catalog # A17693) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MSLNL at approximately 75 kDa. The expected band size for MSLNL is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17693-mslnl-primary-antibodies-ihc-testing-2.jpgAnti-MSLNL Antibody Picoband® IHC analysis of MSLNL using anti-MSLNL antibody (A17693). MSLNL was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MSLNL Antibody (A17693) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17693-mslnl-primary-antibodies-if-testing-3.jpgAnti-MSLNL Antibody Picoband® IF analysis of MSLNL using anti-MSLNL antibody (A15750-1). MSLNL was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MSLNL Antibody (A15750-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17693-mslnl-primary-antibodies-fcm-testing-4.pngAnti-MSLNL Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MSLNL antibody (A17693). Overlay histogram showing JK cells stained with A17693 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MSLNL Antibody (A17693, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mtcl1-picoband-trade-antibody-a10954-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10954-1-mtcl1-primary-antibodies-wb-testing-1.jpgAnti-MTCL1 Antibody Picoband® Western blot analysis of MTCL1 using anti-MTCL1 antibody (A10954-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: rat lung tissue lysates, Lane 3: rat ovary tissue lysates, Lane 4: mouse lung tissue lysates, Lane 5: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTCL1 antigen affinity purified polyclonal antibody (Catalog # A10954-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MTCL1 at approximately 270-300 kDa. The expected band size for MTCL1 is at 210 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10954-1-mtcl1-primary-antibodies-ihc-testing-2.jpgAnti-MTCL1 Antibody Picoband® IHC analysis of MTCL1 using anti-MTCL1 antibody (A10954-1). MTCL1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTCL1 Antibody (A10954-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10954-1-mtcl1-primary-antibodies-ihc-testing-3.jpgAnti-MTCL1 Antibody Picoband® IHC analysis of MTCL1 using anti-MTCL1 antibody (A10954-1). MTCL1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTCL1 Antibody (A10954-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10954-1-mtcl1-primary-antibodies-ihc-testing-4.jpgAnti-MTCL1 Antibody Picoband® IHC analysis of MTCL1 using anti-MTCL1 antibody (A10954-1). MTCL1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTCL1 Antibody (A10954-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10954-1-mtcl1-primary-antibodies-fcm-testing-5.pngAnti-MTCL1 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-MTCL1 antibody (A10954-1). Overlay histogram showing U20S cells stained with A10954-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MTCL1 Antibody (A10954-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-myt1l-picoband-trade-antibody-a07880-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07880-1-myt1l-primary-antibodies-wb-testing-1.jpgAnti-MYT1L Antibody Picoband® Western blot analysis of MYT1L using anti-MYT1L antibody (A07880-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYT1L antigen affinity purified polyclonal antibody (Catalog # A07880-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYT1L at approximately 133 kDa. The expected band size for MYT1L is at 133 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07880-1-myt1l-primary-antibodies-if-testing-2.jpgAnti-MYT1L Antibody Picoband® IF analysis of MYT1L using anti-MYT1L antibody (A07880-1). MYT1L was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MYT1L Antibody (A07880-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07880-1-myt1l-primary-antibodies-fcm-testing-3.pngAnti-MYT1L Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MYT1L antibody (A07880-1). Overlay histogram showing HepG2 cells stained with A07880-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYT1L Antibody (A07880-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-l1td1-picoband-trade-antibody-a12503-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12503-1-l1td1-primary-antibodies-wb-testing-1.jpgAnti-L1TD1 Antibody Picoband® Western blot analysis of L1TD1 using anti-L1TD1 antibody (A12503-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: rat testis lysates, Lane 3: rat C6 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-L1TD1 antigen affinity purified polyclonal antibody (Catalog # A12503-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for L1TD1 at approximately 120 kDa. The expected band size for L1TD1 is at 120 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-ppp1r13b-picoband-trade-antibody-a07257-2-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07257-2-ppp1r13b-primary-antibodies-wb-testing-1.jpgAnti-PPP1R13B Antibody Picoband® Western blot analysis of PPP1R13B using anti-PPP1R13B antibody (A07257-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP1R13B antigen affinity purified polyclonal antibody (Catalog # A07257-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPP1R13B at approximately 150 kDa. The expected band size for PPP1R13B is at 120 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-matr3-picoband-trade-antibody-a02931-2-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-wb-testing-1.jpgAnti-MATR3 Antibody Picoband® Western blot analysis of MATR3 using anti-MATR3 antibody (A02931-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MATR3 antigen affinity purified polyclonal antibody (Catalog # A02931-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MATR3 at approximately 125 kDa. The expected band size for MATR3 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-2.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-3.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-4.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-5.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-6.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-7.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-8.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-ihc-testing-9.jpgAnti-MATR3 Antibody Picoband® IHC analysis of MATR3 using anti-MATR3 antibody (A02931-2). MATR3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATR3 Antibody (A02931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-if-testing-10.jpgAnti-MATR3 Antibody Picoband® IF analysis of MATR3 using anti-MATR3 antibody (A02931-2) and anti-Beta Tubulin antibody (M01857-3). MATR3 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MATR3 Antibody (A02931-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02931-2-matr3-primary-antibodies-fcm-testing-11.pngAnti-MATR3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MATR3 antibody (A02931-2). Overlay histogram showing HepG2 cells stained with A02931-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MATR3 Antibody (A02931-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mccc1-picoband-trade-antibody-a07441-1-boster.html2026-03-17T05:15:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07441-1-mccc1-primary-antibodies-wb-testing-1_1.jpgAnti-MCCC1 Antibody Picoband® Western blot analysis of MCCC1 using anti-MCCC1 antibody (A07441-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat heart tissue lysates, Lane 3: mouse liver tissue lysates, Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCCC1 antigen affinity purified polyclonal antibody (Catalog # A07441-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MCCC1 at approximately 80 kDa. The expected band size for MCCC1 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07441-1-mccc1-primary-antibodies-ihc-testing-2_1.jpgAnti-MCCC1 Antibody Picoband® IHC analysis of MCCC1 using anti-MCCC1 antibody (A07441-1). MCCC1 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC1 Antibody (A07441-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07441-1-mccc1-primary-antibodies-if-testing-3.jpgAnti-MCCC1 Antibody Picoband® IF analysis of MCCC1 using anti-MCCC1 antibody (A07441-1) and anti-Beta Tubulin antibody (M01857-3). MCCC1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MCCC1 Antibody (A07441-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-mccc2-picoband-trade-antibody-a06515-2-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-wb-testing-1.jpgAnti-MCCC2 Antibody Picoband® Western blot analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCCC2 antigen affinity purified polyclonal antibody (Catalog # A06515-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MCCC2 at approximately 61 kDa. The expected band size for MCCC2 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-ihc-testing-2.jpgAnti-MCCC2 Antibody Picoband® IHC analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). MCCC2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC2 Antibody (A06515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-ihc-testing-3.jpgAnti-MCCC2 Antibody Picoband® IHC analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). MCCC2 was detected in a paraffin-embedded section of human intestinal diffuse large B-cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC2 Antibody (A06515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-ihc-testing-4.jpgAnti-MCCC2 Antibody Picoband® IHC analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). MCCC2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC2 Antibody (A06515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-ihc-testing-5.jpgAnti-MCCC2 Antibody Picoband® IHC analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). MCCC2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC2 Antibody (A06515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-ihc-testing-6.jpgAnti-MCCC2 Antibody Picoband® IHC analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). MCCC2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC2 Antibody (A06515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-ihc-testing-7.jpgAnti-MCCC2 Antibody Picoband® IHC analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). MCCC2 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC2 Antibody (A06515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-ihc-testing-8.jpgAnti-MCCC2 Antibody Picoband® IHC analysis of MCCC2 using anti-MCCC2 antibody (A06515-2). MCCC2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MCCC2 Antibody (A06515-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06515-2-mccc2-primary-antibodies-fcm-testing-9.pngAnti-MCCC2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MCCC2 antibody (A06515-2). Overlay histogram showing MCF-7 cells stained with A06515-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MCCC2 Antibody (A06515-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-map1s-picoband-trade-antibody-a04308-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04308-map1s-primary-antibodies-wb-testing-1.jpgAnti-MAP1S Antibody Picoband® Western blot analysis of MAP1S using anti-MAP1S antibody (A04308). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP1S antigen affinity purified polyclonal antibody (Catalog # A04308) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP1S at approximately 150 kDa. The expected band size for MAP1S is at 112 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04308-map1s-primary-antibodies-ihc-testing-2.jpgAnti-MAP1S Antibody Picoband® IHC analysis of MAP1S using anti-MAP1S antibody (A04308). MAP1S was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP1S Antibody (A04308) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04308-map1s-primary-antibodies-ihc-testing-3.jpgAnti-MAP1S Antibody Picoband® IHC analysis of MAP1S using anti-MAP1S antibody (A04308). MAP1S was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP1S Antibody (A04308) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04308-map1s-primary-antibodies-fcm-testing-4.pngAnti-MAP1S Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-MAP1S antibody (A04308). Overlay histogram showing PC-3 cells stained with A04308 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAP1S Antibody (A04308, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mansc1-picoband-trade-antibody-a15720-2-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15720-2-mansc1-primary-antibodies-wb-testing-1.jpgAnti-MANSC1 Antibody Picoband® Western blot analysis of MANSC1 using anti-MANSC1 antibody (A15720-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MANSC1 antigen affinity purified polyclonal antibody (Catalog # A15720-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MANSC1 at approximately 62 kDa. The expected band size for MANSC1 is at 62 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-melk-picoband-trade-antibody-a04038-2-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04038-2-melk-primary-antibodies-wb-testing-1.jpgAnti-MELK Antibody Picoband® Western blot analysis of MELK using anti-MELK antibody (A04038-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human U87 whole cell lysates, Lane 5: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MELK antigen affinity purified polyclonal antibody (Catalog # A04038-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MELK at approximately 66 kDa. The expected band size for MELK is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04038-2-melk-primary-antibodies-ihc-testing-2.jpgAnti-MELK Antibody Picoband® IHC analysis of MELK using anti-MELK antibody (A04038-2). MELK was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELK Antibody (A04038-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04038-2-melk-primary-antibodies-ihc-testing-3.jpgAnti-MELK Antibody Picoband® IHC analysis of MELK using anti-MELK antibody (A04038-2). MELK was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELK Antibody (A04038-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04038-2-melk-primary-antibodies-if-testing-4.jpgAnti-MELK Antibody Picoband® IF analysis of MELK using anti-MELK antibody (A04038-2). MELK was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MELK Antibody (A04038-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04038-2-melk-primary-antibodies-fcm-testing-5.pngAnti-MELK Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MELK antibody (A04038-2). Overlay histogram showing JK cells stained with A04038-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MELK Antibody (A04038-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nsfl1c-picoband-trade-antibody-a08116-1-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08116-1-nsfl1c-primary-antibodies-wb-testing-1.jpgAnti-NSFL1C Antibody Picoband® Western blot analysis of NSFL1C using anti-NSFL1C antibody (A08116-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: rat RH35 whole cell lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSFL1C antigen affinity purified polyclonal antibody (Catalog # A08116-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSFL1C at approximately 41 kDa. The expected band size for NSFL1C is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08116-1-nsfl1c-primary-antibodies-if-testing-2.jpgAnti-NSFL1C Antibody Picoband® IF analysis of NSFL1C using anti-NSFL1C antibody (A08116-1) and anti-Beta Tubulin antibody (M01857-3). NSFL1C was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NSFL1C Antibody (A08116-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08116-1-nsfl1c-primary-antibodies-fcm-testing-3.pngAnti-NSFL1C Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NSFL1C antibody (A08116-1). Overlay histogram showing 293T cells stained with A08116-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSFL1C Antibody (A08116-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mppe1-picoband-trade-antibody-a12491-1-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12491-1-mppe1-primary-antibodies-wb-testing-1.jpgAnti-MPPE1 Antibody Picoband® Western blot analysis of MPPE1 using anti-MPPE1 antibody (A12491-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPPE1 antigen affinity purified polyclonal antibody (Catalog # A12491-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MPPE1 at approximately 45 kDa. The expected band size for MPPE1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12491-1-mppe1-primary-antibodies-fcm-testing-2.pngAnti-MPPE1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-MPPE1 antibody (A12491-1). Overlay histogram showing RT4 cells stained with A12491-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MPPE1 Antibody (A12491-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mpst-picoband-trade-antibody-a04609-1-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04609-1-mpst-primary-antibodies-wb-testing-1.jpgAnti-MPST Antibody Picoband® Western blot analysis of MPST using anti-MPST antibody (A04609-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPST antigen affinity purified polyclonal antibody (Catalog # A04609-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MPST at approximately 33 kDa. The expected band size for MPST is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04609-1-mpst-primary-antibodies-if-testing-2.jpgAnti-MPST Antibody Picoband® IF analysis of MPST using anti-MPST antibody (A04609-1). MPST was detected in an immunocytochemical section of PC3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MPST Antibody (A04609-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04609-1-mpst-primary-antibodies-fcm-testing-3.pngAnti-MPST Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-MPST antibody (A04609-1). Overlay histogram showing SH-SY5Y cells stained with A04609-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MPST Antibody (A04609-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mllt10-picoband-trade-antibody-a04471-2-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04471-2-mllt10-primary-antibodies-wb-testing-1.jpgAnti-MLLT10 Antibody Picoband® Western blot analysis of MLLT10 using anti-MLLT10 antibody (A04471-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MLLT10 antigen affinity purified polyclonal antibody (Catalog # A04471-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MLLT10 at approximately 130 kDa. The expected band size for MLLT10 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04471-2-mllt10-primary-antibodies-if-testing-2.jpgAnti-MLLT10 Antibody Picoband® IF analysis of MLLT10 using anti-MLLT10 antibody (A04471-2) and anti-Beta Tubulin antibody (M01857-3). MLLT10 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MLLT10 Antibody (A04471-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04471-2-mllt10-primary-antibodies-fcm-testing-3.pngAnti-MLLT10 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-MLLT10 antibody (A04471-2). Overlay histogram showing PC-3 cells stained with A04471-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MLLT10 Antibody (A04471-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mlst8-picoband-trade-antibody-a05357-2-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-wb-testing-1.jpgAnti-MLST8 Antibody Picoband® Western blot analysis of MLST8 using anti-MLST8 antibody (A05357-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MLST8 antigen affinity purified polyclonal antibody (Catalog # A05357-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MLST8 at approximately 36 kDa. The expected band size for MLST8 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-ihc-testing-2.jpgAnti-MLST8 Antibody Picoband® IHC analysis of MLST8 using anti-MLST8 antibody (A05357-2). MLST8 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLST8 Antibody (A05357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-ihc-testing-3.jpgAnti-MLST8 Antibody Picoband® IHC analysis of MLST8 using anti-MLST8 antibody (A05357-2). MLST8 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLST8 Antibody (A05357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-ihc-testing-4.jpgAnti-MLST8 Antibody Picoband® IHC analysis of MLST8 using anti-MLST8 antibody (A05357-2). MLST8 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLST8 Antibody (A05357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-ihc-testing-5.jpgAnti-MLST8 Antibody Picoband® IHC analysis of MLST8 using anti-MLST8 antibody (A05357-2). MLST8 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLST8 Antibody (A05357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-ihc-testing-6.jpgAnti-MLST8 Antibody Picoband® IHC analysis of MLST8 using anti-MLST8 antibody (A05357-2). MLST8 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLST8 Antibody (A05357-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-if-testing-7.jpgAnti-MLST8 Antibody Picoband® IF analysis of MLST8 using anti-MLST8 antibody (A05357-2) and anti-Beta Tubulin antibody (M01857-3). MLST8 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MLST8 Antibody (A05357-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-if-testing-8.jpgAnti-MLST8 Antibody Picoband® IF analysis of MLST8 using anti-MLST8 antibody (A05357-2). MLST8 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MLST8 Antibody (A05357-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-if-testing-9.jpgAnti-MLST8 Antibody Picoband® IF analysis of MLST8 using anti-MLST8 antibody (A05357-2). MLST8 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MLST8 Antibody (A05357-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05357-2-mlst8-primary-antibodies-fcm-testing-10.pngAnti-MLST8 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-MLST8 antibody (A05357-2). Overlay histogram showing SiHa cells stained with A05357-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MLST8 Antibody (A05357-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-dapk1-picoband-trade-antibody-a01161-1-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01161-1-dapk1-primary-antibodies-wb-testing-1.jpgAnti-DAPK1 Antibody Picoband® Western blot analysis of DAPK1 using anti-DAPK1 antibody (A01161-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DAPK1 antigen affinity purified polyclonal antibody (Catalog # A01161-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DAPK1 at approximately 160 kDa. The expected band size for DAPK1 is at 160 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01161-1-dapk1-primary-antibodies-ihc-testing-2.jpgAnti-DAPK1 Antibody Picoband® IHC analysis of DAPK1 using anti-DAPK1 antibody (A01161-1). DAPK1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DAPK1 Antibody (A01161-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01161-1-dapk1-primary-antibodies-ihc-testing-3.jpgAnti-DAPK1 Antibody Picoband® IHC analysis of DAPK1 using anti-DAPK1 antibody (A01161-1). DAPK1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DAPK1 Antibody (A01161-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01161-1-dapk1-primary-antibodies-ihc-testing-4.jpgAnti-DAPK1 Antibody Picoband® IHC analysis of DAPK1 using anti-DAPK1 antibody (A01161-1). DAPK1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DAPK1 Antibody (A01161-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-mogat2-picoband-trade-antibody-a10993-2-boster.html2026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-wb-testing-1.jpgAnti-MOGAT2 Antibody Picoband® Western blot analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOGAT2 antigen affinity purified polyclonal antibody (Catalog # A10993-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOGAT2 at approximately 43 kDa. The expected band size for MOGAT2 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-ihc-testing-2.jpgAnti-MOGAT2 Antibody Picoband® IHC analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). MOGAT2 was detected in a paraffin-embedded section of human prostatic acinar adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOGAT2 Antibody (A10993-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-ihc-testing-3.jpgAnti-MOGAT2 Antibody Picoband® IHC analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). MOGAT2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOGAT2 Antibody (A10993-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-ihc-testing-4.jpgAnti-MOGAT2 Antibody Picoband® IHC analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). MOGAT2 was detected in a paraffin-embedded section of human testicular germ cell tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOGAT2 Antibody (A10993-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-ihc-testing-5.jpgAnti-MOGAT2 Antibody Picoband® IHC analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). MOGAT2 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOGAT2 Antibody (A10993-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-ihc-testing-6.jpgAnti-MOGAT2 Antibody Picoband® IHC analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). MOGAT2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOGAT2 Antibody (A10993-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-ihc-testing-7.jpgAnti-MOGAT2 Antibody Picoband® IHC analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). MOGAT2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOGAT2 Antibody (A10993-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-if-testing-8.jpgAnti-MOGAT2 Antibody Picoband® IF analysis of MOGAT2 using anti-MOGAT2 antibody (A10993-2). MOGAT2 was detected in an immunocytochemical section of HepG2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MOGAT2 Antibody (A10993-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10993-2-mogat2-primary-antibodies-fcm-testing-9.pngAnti-MOGAT2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MOGAT2 antibody (A10993-2). Overlay histogram showing HepG2 cells stained with A10993-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOGAT2 Antibody (A10993-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mospd2-picoband-trade-antibody-a16695-1-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-wb-testing-1_1.jpgAnti-MOSPD2 Antibody Picoband® Western blot analysis of MOSPD2 using anti-MOSPD2 antibody (A16695-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: rat RH35 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse Neuro-2a whole cell lysates, Lane 7: mouse HEPA1-6 whole cell lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOSPD2 antigen affinity purified polyclonal antibody (Catalog # A16695-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOSPD2 at approximately 60 kDa. The expected band size for MOSPD2 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-ihc-testing-2.jpgAnti-MOSPD2 Antibody Picoband® IHC analysis of MOSPD2 using anti-MOSPD2 antibody (A16695-1). MOSPD2 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOSPD2 Antibody (A16695-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-ihc-testing-3.jpgAnti-MOSPD2 Antibody Picoband® IHC analysis of MOSPD2 using anti-MOSPD2 antibody (A16695-1). MOSPD2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOSPD2 Antibody (A16695-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-ihc-testing-4.jpgAnti-MOSPD2 Antibody Picoband® IHC analysis of MOSPD2 using anti-MOSPD2 antibody (A16695-1). MOSPD2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOSPD2 Antibody (A16695-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-ihc-testing-5.jpgAnti-MOSPD2 Antibody Picoband® IHC analysis of MOSPD2 using anti-MOSPD2 antibody (A16695-1). MOSPD2 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOSPD2 Antibody (A16695-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-ihc-testing-6.jpgAnti-MOSPD2 Antibody Picoband® IHC analysis of MOSPD2 using anti-MOSPD2 antibody (A16695-1). MOSPD2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOSPD2 Antibody (A16695-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-ihc-testing-7.jpgAnti-MOSPD2 Antibody Picoband® IHC analysis of MOSPD2 using anti-MOSPD2 antibody (A16695-1). MOSPD2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MOSPD2 Antibody (A16695-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-fcm-testing-8.pngAnti-MOSPD2 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-MOSPD2 antibody (A16695-1). Overlay histogram showing Caco-2 cells stained with A16695-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOSPD2 Antibody (A16695-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16695-1-mospd2-primary-antibodies-fcm-testing-9.pngAnti-MOSPD2 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MOSPD2 antibody (A16695-1). Overlay histogram showing Hela cells stained with A16695-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOSPD2 Antibody (A16695-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rtn4ip1-picoband-trade-antibody-a13135-1-boster.html2026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13135-1-rtn4ip1-primary-antibodies-wb-testing-1.jpgAnti-RTN4IP1 Antibody Picoband® Western blot analysis of RTN4IP1 using anti-RTN4IP1 antibody (A13135-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse kidney tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RTN4IP1 antigen affinity purified polyclonal antibody (Catalog # A13135-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RTN4IP1 at approximately 44 kDa. The expected band size for RTN4IP1 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13135-1-rtn4ip1-primary-antibodies-fcm-testing-2.pngAnti-RTN4IP1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-RTN4IP1 antibody (A13135-1). Overlay histogram showing K562 cells stained with A13135-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RTN4IP1 Antibody (A13135-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1241802026-03-16T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-4-krt15-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 15/KRT15 AntibodyWestern blot analysis of Cytokeratin 15/KRT15 using anti-Cytokeratin 15/KRT15 antibody (A06791-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 15/KRT15 antigen affinity purified polyclonal antibody (A06791-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Cytokeratin 15/KRT15 at approximately 49 kDa. The expected band size for Cytokeratin 15/KRT15 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-4-krt15-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 15/KRT15 AntibodyIHC analysis of Cytokeratin 15/KRT15 using anti-Cytokeratin 15/KRT15 antibody (A06791-4). Cytokeratin 15/KRT15 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Cytokeratin 15/KRT15 Antibody (A06791-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-4-krt15-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 15/KRT15 AntibodyIHC analysis of Cytokeratin 15/KRT15 using anti-Cytokeratin 15/KRT15 antibody (A06791-4). Cytokeratin 15/KRT15 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Cytokeratin 15/KRT15 Antibody (A06791-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-4-krt15-primary-antibodies-ihc-testing-3.jpgAnti-Cytokeratin 15/KRT15 AntibodyIHC analysis of Cytokeratin 15/KRT15 using anti-Cytokeratin 15/KRT15 antibody (A06791-4). Cytokeratin 15/KRT15 was detected in a paraffin-embedded section of mouse skin tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Cytokeratin 15/KRT15 Antibody (A06791-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06791-4-krt15-primary-antibodies-ihc-testing-4.jpgAnti-Cytokeratin 15/KRT15 AntibodyIHC analysis of Cytokeratin 15/KRT15 using anti-Cytokeratin 15/KRT15 antibody (A06791-4). Cytokeratin 15/KRT15 was detected in a paraffin-embedded section of rat skin tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Cytokeratin 15/KRT15 Antibody (A06791-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1241812026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00880-2-myh9-primary-antibodies-wb-testing-1.jpgAnti-MYH9 Antibody Picoband®Western blot analysis of MYH9 using anti-MYH9 antibody (A00880-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYH9 antigen affinity purified polyclonal antibody (A00880-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MYH9 at approximately 220-250 kDa. The expected band size for MYH9 is at 227 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00880-2-myh9-primary-antibodies-ihc-testing-1.jpgAnti-MYH9 Antibody Picoband®IHC analysis of MYH9 using anti-MYH9 antibody (A00880-2). MYH9 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH9 Antibody (A00880-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00880-2-myh9-primary-antibodies-ihc-testing-2.jpgAnti-MYH9 Antibody Picoband®IHC analysis of MYH9 using anti-MYH9 antibody (A00880-2). MYH9 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH9 Antibody (A00880-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00880-2-myh9-primary-antibodies-if-testing-1.jpgAnti-MYH9 Antibody Picoband®IF analysis of MYH9 using anti-MYH9 antibody (A00880-2). MYH9 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MYH9 Antibody (A00880-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00880-2-myh9-primary-antibodies-if-testing-2.jpgAnti-MYH9 Antibody Picoband®IF analysis of MYH9 using anti-MYH9 antibody (A00880-2). MYH9 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MYH9 Antibody (A00880-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00880-2-myh9-primary-antibodies-ip-testing-1.jpgAnti-MYH9 Antibody Picoband®Immunoprecipitating MYH9 in A549 whole cell lysate. Western blot analysis of MYH9 using anti-MYH9 antibody (A00880-2). Lane 1: A549 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-MYH9 antibody in A549 whole cell lysate, Lane 3: anti-MYH9 antibody (2μg) + A549 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MYH9 antigen affinity purified polyclonal antibody (A00880-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for MYH9 at approximately 250 kDa. The expected band size for MYH9 is at 227 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00880-2-myh9-primary-antibodies-fcm-testing-1.jpgAnti-MYH9 Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-MYH9 antibody (A00880-2). Overlay histogram showing U251 cells stained with A00880-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MYH9 Antibody (A00880-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1241822026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08015-1-p4ha2-primary-antibodies-wb-testing-1.jpgAnti-P4HA2 Antibody Picoband®Western blot analysis of P4HA2 using anti-P4HA2 antibody (A08015-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P4HA2 antigen affinity purified polyclonal antibody (A08015-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P4HA2 at approximately 61 kDa. The expected band size for P4HA2 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08015-1-p4ha2-primary-antibodies-fcm-testing-1.jpgAnti-P4HA2 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-P4HA2 antibody (A08015-1). Overlay histogram showing 293T cells stained with A08015-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-P4HA2 Antibody (A08015-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1241832026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241842026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241852026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05044-2-fgl1-primary-antibodies-wb-testing-1.jpgAnti-FGL1 Antibody Picoband® Western blot analysis of FGL1 using anti-FGL1 antibody (A05044-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates, Lane 4: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGL1 antigen affinity purified polyclonal antibody (A05044-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FGL1 at approximately 36 kDa. The expected band size for FGL1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05044-2-fgl1-primary-antibodies-ihc-testing-1.jpgAnti-FGL1 Antibody Picoband®IHC analysis of FGL1 using anti-FGL1 antibody (A05044-2). FGL1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FGL1 Antibody (A05044-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1241862026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241872026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241882026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04140-3-rbm4-primary-antibodies-wb-testing-1.jpgAnti-RBM4 Antibody Picoband®Western blot analysis of RBM4 using anti-RBM4 antibody (A04140-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBM4 antigen affinity purified polyclonal antibody (A04140-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RBM4 at approximately 45 kDa. The expected band size for RBM4 is at 40 kDa. https://www.bosterbio.com/catalog/product/view/id/1241892026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241902026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241912026-03-16T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04296-2-wtap-primary-antibodies-wb-testing-1.jpgAnti-WTAP Antibody Western blot analysis of WTAP using anti-WTAP antibody (A04296-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse NRK whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-WTAP antigen affinity purified polyclonal antibody (A04296-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for WTAP at approximately 50 kDa. The expected band size for WTAP is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04296-2-41598_2025_88671_fig1_html.pngAnti-WTAP AntibodyThe relationship of m6A regulators, immune score and clustering of TCGA-GBM patients according to the expression of WTAP and ZC3H13. The correlation between m6A regulators and results of ESTIMATE ( A ). The expression of WTAP and ZC3H13in GBM ( n = 144) and the corresponding normal tissue ( n = 10), respectively ( B and C ). The heatmap of two clusters (group1 = 79, group2 = 65) according to the expression WTAP and ZC3H13 in TCGA-GBM ( D ).The association between the expression of WTAP and ZC3H13 ( E ). The data are mean ± standard deviation. ** P < 0.01 compared with the corresponding control values. Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-88671-4'>39910141</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04296-2-41598_2025_88671_fig7_html.pngAnti-WTAP AntibodyThe validation of immune character between two clusters in GEO data. The headmap of expression of WTAP and ZC3H13 in two clusters ( A ). The association between WTAP and ZC3H13 in GSE108474 and GSE50161 ( B ). The correlation of stromal score, immune score, ESTIMATE score and tumor purity in two clusters ( C ).The targets of immunomodulatory ( D ). The proportion of immune cells ( E ) and expression of immune cells ( F ) between two clusters. The number of cluster1 is 79, and cluster2 is 65. The data are mean ± standard deviation (ns, no significance, *P < 0.05 compared with the corresponding control values). Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-88671-4'>39910141</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04296-2-41598_2025_88671_fig8_html.pngAnti-WTAP AntibodyThe validation of immune character between two clusters in CGGA data. The headmap of expression of WTAP and ZC3H13 in two clusters ( A ). The association between WTAP and ZC3H13 in CGGA data ( B ). The correlation of stromal score, immune score, ESTIMATE score and tumor purity in two clusters ( C ).The targets of immunomodulatory ( D ). The proportion of immune cells ( E ) and expression of immune cells (F) between two clusters. The number of cluster1 is 446, and cluster2 is 572. The data are mean ± standard deviation (ns, no significance, *P < 0.05, **P < 0.01 and ***P < 0.001 compared with the corresponding control values). Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-88671-4'>39910141</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04296-2-41598_2025_88671_fig9_html.pngAnti-WTAP AntibodyRelative expression of genes expression in GBM tissues. Expression levels of WTAP and ZC3H13 genes were compared with those of the control group on GBM tissues, 10 GBM and adjacent tissues, respectively ( A ). The expression levels of siRNA WTAP and overexpression ZC3H13 genes ( B and C ). The expression levels of CD27, CD70, CD80, CD86, ICOS, CTLA4, and LAG3 in siRNA WTAP and overexpression ZC3H13 were demonstrated in Fig. D and F, respectively. The result were determined by qRT-PCR. The data are mean ± standard deviation of six replicate experiments. * P < 0.05, **P < 0.01 and ***P < 0.001 compared with the corresponding control values. Index in PubMed under a CC BY license. PMID: <a href='https://idp.nature.com/authorize?response_type=cookie&client_id=grover&redirect_uri=https%3A%2F%2Fwww.nature.com%2Farticles%2Fs41598-025-88671-4'>39910141</a> https://www.bosterbio.com/catalog/product/view/id/1241922026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00263-2-mda5-ifih1-primary-antibodies-wb-testing-1.jpgAnti-MDA5/IFIH1 Antibody Western blot analysis of MDA5/IFIH1 using anti-MDA5/IFIH1 antibody (A00263-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Raji whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MDA5/IFIH1 antigen affinity purified polyclonal antibody (A00263-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MDA5/IFIH1 at approximately 125 kDa. The expected band size for MDA5/IFIH1 is at 117 kDa. https://www.bosterbio.com/catalog/product/view/id/1241932026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03104-2-rbm3-primary-antibodies-wb-testing-1.jpgAnti-RBM3 Antibody Picoband®Western blot analysis of RBM3 using anti-RBM3 antibody (A03104-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Raji whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBM3 antigen affinity purified polyclonal antibody (A03104-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RBM3 at approximately 22 kDa. The expected band size for RBM3 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03104-2-rbm3-primary-antibodies-fcm-testing-1.jpgAnti-RBM3 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-RBM3 antibody (A03104-2). Overlay histogram showing MCF-7 cells stained with A03104-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RBM3 Antibody (A03104-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1241942026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241952026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241962026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-2-pyruvate-carboxylase-pc-primary-antibodies-wb-testing-1.jpgAnti-Pyruvate Carboxylase/PC Antibody Western blot analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human SiHa whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH-35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Pyruvate Carboxylase/PC antigen affinity purified polyclonal antibody (A03853-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Pyruvate Carboxylase/PC at approximately 130 kDa. The expected band size for Pyruvate Carboxylase/PC is at 130 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-2-pc-primary-antibodies-ihc-testing-1.jpgAnti-Pyruvate Carboxylase/PC AntibodyIHC analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-2). Pyruvate Carboxylase/PC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-2-pc-primary-antibodies-ihc-testing-2.jpgAnti-Pyruvate Carboxylase/PC AntibodyIHC analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-2). Pyruvate Carboxylase/PC was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-2-pyruvate-carboxylase-pc-primary-antibodies-if-testing-1.jpgAnti-Pyruvate Carboxylase/PC AntibodyIF analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-2). Pyruvate Carboxylase/PC was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1241972026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1241982026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07547-1-gpt2-primary-antibodies-wb-testing-1.jpgAnti-GPT2 Antibody Picoband®Western blot analysis of GPT2 using anti-GPT2 antibody (A07547-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat kidney tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse kidney tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GPT2 antigen affinity purified polyclonal antibody (A07547-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GPT2 at approximately 58 kDa. The expected band size for GPT2 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07547-1-gpt2-primary-antibodies-if-testing-1.jpgAnti-GPT2 Antibody Picoband®IF analysis of GPT2 using anti-GPT2 antibody (A07547-1). GPT2 was detected in an immunocytochemical section of HepG2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GPT2 Antibody (A07547-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1241992026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242002026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242012026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242022026-03-17T05:15:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05311-2-mpp5-pals1-primary-antibodies-wb-testing-1.jpgAnti-MPP5/PALS1 Antibody Picoband® Western blot analysis of MPP5/PALS1 using anti-MPP5/PALS1 antibody (A05311-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cellue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cellsue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPP5/PALS1 antigen affinity purified polyclonal antibody (A05311-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MPP5/PALS1 at approximately 80 kDa. The expected band size for MPP5/PALS1 is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05311-2-mpp5-pals1-primary-antibodies-ihc-testing-2.jpgAnti-MPP5/PALS1 Antibody Picoband® IHC analysis of MPP5/PALS1 using anti-MPP5/PALS1 antibody (A05311-2). MPP5/PALS1 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MPP5/PALS1 Antibody (A05311-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05311-2-mpp5-pals1-primary-antibodies-ihc-testing-3.jpgAnti-MPP5/PALS1 Antibody Picoband® IHC analysis of MPP5/PALS1 using anti-MPP5/PALS1 antibody (A05311-2). MPP5/PALS1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MPP5/PALS1 Antibody (A05311-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05311-2-mpp5-pals1-primary-antibodies-ip-testing-4.jpgAnti-MPP5/PALS1 Antibody Picoband® Immunoprecipitating MPP5/PALS1 in HepG2 whole cell lysate. Western blot analysis of MPP5/PALS1 using anti-MPP5/PALS1 antibody (A05311-2). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-MPP5/PALS1 antibody in HepG2 whole cell lysate, Lane 3: anti-MPP5/PALS1 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MPP5/PALS1 antigen affinity purified polyclonal antibody (A05311-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Light Chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for MPP5/PALS1 at approximately 80 kDa. The expected band size for MPP5/PALS1 is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05311-2-mpp5-pals1-primary-antibodies-fcm-testing-5.jpgAnti-MPP5/PALS1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MPP5/PALS1 antibody (A05311-2). Overlay histogram showing 293T cells stained with A05311-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MPP5/PALS1 Antibody (A05311-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242032026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242042026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05857-2-ppat-primary-antibodies-wb-testing-1.jpgAnti-PPAT Antibody Picoband®Western blot analysis of PPAT using anti-PPAT antibody (A05857-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPAT antigen affinity purified polyclonal antibody (A05857-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PPAT at approximately 57 kDa. The expected band size for PPAT is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05857-2-ppat-primary-antibodies-if-testing-1.jpgAnti-PPAT Antibody Picoband®IF analysis of PPAT using anti-PPAT antibody (A05857-2). PPAT was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PPAT Antibody (A05857-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05857-2-ppat-primary-antibodies-fcm-testing-1.jpgAnti-PPAT Antibody Picoband®Flow Cytometry analysis of K562 cells using anti-PPAT antibody (A05857-2). Overlay histogram showing K562 cells stained with A05857-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPAT Antibody (A05857-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242052026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04913-2-exoc2-primary-antibodies-wb-testing-1.jpgAnti-SEC5/EXOC2 Antibody Picoband®Western blot analysis of SEC5/EXOC2 using anti-SEC5/EXOC2 antibody (A04913-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse Neuro-2a whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SEC5/EXOC2 antigen affinity purified polyclonal antibody (A04913-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SEC5/EXOC2 at approximately 100 kDa. The expected band size for SEC5/EXOC2 is at 104 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04913-2-exoc2-primary-antibodies-ihc-testing-1.jpgAnti-SEC5/EXOC2 Antibody Picoband®IHC analysis of SEC5/EXOC2 using anti-SEC5/EXOC2 antibody (A04913-2). SEC5/EXOC2 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SEC5/EXOC2 Antibody (A04913-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04913-2-exoc2-primary-antibodies-if-testing-1.jpgAnti-SEC5/EXOC2 Antibody Picoband®IF analysis of SEC5/EXOC2 using anti-SEC5/EXOC2 antibody (A04913-2) and anti-Alpha Tubulin antibody (M03989-3). SEC5/EXOC2 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SEC5/EXOC2 Antibody (A04913-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1242062026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242072026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242082026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01634-1-galc-primary-antibodies-wb-testing-1.jpgAnti-GALC Antibody Picoband® Western blot analysis of GALC using anti-GALC antibody (A01634-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALC antigen affinity purified polyclonal antibody (A01634-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GALC at approximately 90 kDa. The expected band size for GALC is at 77 kDa. https://www.bosterbio.com/catalog/product/view/id/1242092026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242102026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00431-2-tcf4-primary-antibodies-wb-testing-1.jpgAnti-TCF4/TCF7L2 AntibodyWestern blot analysis of TCF4 using anti-TCF4 antibody (A00431-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human U2OS whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TCF4 antigen affinity purified polyclonal antibody (A00431-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TCF4 at approximately 72 kDa. The expected band size for TCF4 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00431-2-tcf4-primary-antibodies-ihc-testing-1.jpgAnti-TCF4/TCF7L2 AntibodyIHC analysis of TCF4/TCF7L2 using anti-TCF4/TCF7L2 antibody (A00431-2). TCF4/TCF7L2 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-TCF4/TCF7L2 Antibody (A00431-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00431-2-tcf4-primary-antibodies-ihc-testing-2.jpgAnti-TCF4/TCF7L2 AntibodyIHC analysis of TCF4/TCF7L2 using anti-TCF4/TCF7L2 antibody (A00431-2). TCF4/TCF7L2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-TCF4/TCF7L2 Antibody (A00431-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00431-2-tcf4-primary-antibodies-ihc-testing-3.jpgAnti-TCF4/TCF7L2 AntibodyIHC analysis of TCF4/TCF7L2 using anti-TCF4/TCF7L2 antibody (A00431-2). TCF4/TCF7L2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-TCF4/TCF7L2 Antibody (A00431-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00431-2-tcf4-primary-antibodies-ihc-testing-4.jpgAnti-TCF4/TCF7L2 AntibodyIHC analysis of TCF4 using anti-TCF4 antibody (A00431-2). TCF4 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-TCF4 Antibody (A00431-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242112026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242122026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06354-3-dgka-primary-antibodies-wb-testing-1.jpgAnti-DGKA Antibody Picoband®Western blot analysis of DGKA using anti-DGKA antibody (A06354-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat thymus tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DGKA antigen affinity purified polyclonal antibody (A06354-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DGKA at approximately 90 kDa. The expected band size for DGKA is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06354-3-dgka-primary-antibodies-fcm-testing-1.jpgAnti-DGKA Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-DGKA antibody (A06354-3). Overlay histogram showing Jurkat cells stained with A06354-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DGKA Antibody (A06354-3, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242132026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02248-2-dkk3-primary-antibodies-wb-testing-1.jpgAnti-DKK3 Antibody Western blot analysis of DKK3 using anti-DKK3 antibody (A02248-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DKK3 antigen affinity purified polyclonal antibody (A02248-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DKK3 at approximately 50 kDa. The expected band size for DKK3 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02248-2-dkk3-primary-antibodies-ihc-testing-1.jpgAnti-DKK3 AntibodyIHC analysis of DKK3 using anti-DKK3 antibody (A02248-2). DKK3 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DKK3 Antibody (A02248-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242142026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242162026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05874-3-hspc150-ube2t-primary-antibodies-wb-testing-1.jpgAnti-HSPC150/UBE2T Antibody Picoband® Western blot analysis of HSPC150/UBE2T using anti-HSPC150/UBE2T antibody (A05874-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Skov3 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPC150/UBE2T antigen affinity purified polyclonal antibody (A05874-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HSPC150/UBE2T at approximately 23 kDa. The expected band size for HSPC150/UBE2T is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05874-3-hspc150-ube2t-primary-antibodies-if-testing-2.jpgAnti-HSPC150/UBE2T Antibody Picoband® IF analysis of HSPC150/UBE2T using anti-HSPC150/UBE2T antibody (A05874-3). HSPC150/UBE2T was detected in an immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-HSPC150/UBE2T Antibody (A05874-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05874-3-ube2t-primary-antibodies-wb-testing-1.jpgAnti-HSPC150/UBE2T Antibody Picoband®Western blot analysis of UBE2T using anti-UBE2T antibody (A05874-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SK-OV-3 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UBE2T antigen affinity purified polyclonal antibody (A05874-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UBE2T at approximately 23 kDa. The expected band size for UBE2T is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05874-3-ube2t-primary-antibodies-fcm-testing-1.jpgAnti-HSPC150/UBE2T Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-UBE2T antibody (A05874-3). Overlay histogram showing MCF-7 cells stained with A05874-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-UBE2T Antibody (A05874-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242172026-03-16T05:08:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07816-2-usp13-primary-antibodies-wb-testing-1.jpgAnti-USP13 AntibodyWestern blot analysis of USP13 using anti-USP13 antibody (A07816-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A375 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-USP13 antigen affinity purified polyclonal antibody (A07816-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for USP13 at approximately 100 kDa. The expected band size for USP13 is at 97 kDa. https://www.bosterbio.com/catalog/product/view/id/1242182026-03-13T05:05:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02289-1-cytokeratin-17-krt17-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 17/KRT17-Specific Antibody Western blot analysis of Cytokeratin 17/KRT17 using anti-Cytokeratin 17/KRT17 antibody (A02289-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse NIH/3T3 whole cell lysates, Lane 8: mouse SP2/0 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 17/KRT17 antigen affinity purified polyclonal antibody (A02289-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Cytokeratin 17/KRT17 at approximately 48 kDa. The expected band size for Cytokeratin 17/KRT17 is at 48 kDa. https://www.bosterbio.com/catalog/product/view/id/1242192026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242202026-03-13T05:05:02+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242212026-03-16T05:08:17+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242222026-03-16T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04182-2-fkbp5-primary-antibodies-wb-testing-1.jpgAnti-FKBP5 AntibodyWestern blot analysis of FKBP5 using anti-FKBP5 antibody (A04182-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FKBP5 antigen affinity purified polyclonal antibody (A04182-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FKBP5 at approximately 55 kDa. The expected band size for FKBP5 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04182-2-fkbp5-primary-antibodies-ihc-testing-1.jpgAnti-FKBP5 AntibodyIHC analysis of FKBP5 using anti-FKBP5 antibody (A04182-2). FKBP5 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FKBP5 Antibody (A04182-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04182-2-fkbp5-primary-antibodies-ihc-testing-2.jpgAnti-FKBP5 AntibodyIHC analysis of FKBP5 using anti-FKBP5 antibody (A04182-2). FKBP5 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FKBP5 Antibody (A04182-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04182-2-fkbp5-primary-antibodies-ihc-testing-3.jpgAnti-FKBP5 AntibodyIHC analysis of FKBP5 using anti-FKBP5 antibody (A04182-2). FKBP5 was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FKBP5 Antibody (A04182-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04182-2-fkbp5-primary-antibodies-ihc-testing-4.jpgAnti-FKBP5 AntibodyIHC analysis of FKBP5 using anti-FKBP5 antibody (A04182-2). FKBP5 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FKBP5 Antibody (A04182-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242232026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242242026-03-24T05:36:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09406-3-lamp3-primary-antibodies-wb-testing-1.jpgAnti-LAMP3 AntibodyWestern blot analysis of LAMP3 using anti-LAMP3 antibody (A09406-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Raji whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LAMP3 antigen affinity purified polyclonal antibody (A09406-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LAMP3 at approximately 70 kDa. The expected band size for LAMP3 is at 44 kDa. https://www.bosterbio.com/catalog/product/view/id/1242262026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242272026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06260-oma1-primary-antibodies-wb-testing-1_1.jpgAnti-OMA1 Antibody Picoband®Western blot analysis of OMA1 using anti-OMA1 antibody (A06260). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat skeletal muscle tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OMA1 antigen affinity purified polyclonal antibody (A06260) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for OMA1 at approximately 60 kDa. The expected band size for OMA1 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06260-oma1-primary-antibodies-ihc-testing-1.jpgAnti-OMA1 Antibody Picoband®IHC analysis of OMA1 using anti-OMA1 antibody (A06260). OMA1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OMA1 Antibody (A06260) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06260-oma1-primary-antibodies-ihc-testing-2_1.jpgAnti-OMA1 Antibody Picoband®IHC analysis of OMA1 using anti-OMA1 antibody (A06260). OMA1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OMA1 Antibody (A06260) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06260-oma1-primary-antibodies-if-testing-1.jpgAnti-OMA1 Antibody Picoband®IF analysis of OMA1 using anti-OMA1 antibody (A06260) and anti-Tubulin Alpha antibody (M03989-3). OMA1 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-OMA1 Antibody (A06260) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06260-oma1-primary-antibodies-fcm-testing-1.jpgAnti-OMA1 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-OMA1 antibody (A06260). Overlay histogram showing HepG2 cells stained with A06260 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-OMA1 Antibody (A06260, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242282026-03-16T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08193-1-pacs2-primary-antibodies-wb-testing-1.jpgAnti-PACS2-Specific Antibody Western blot analysis of PACS2 using anti-PACS2 antibody (A08193-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PACS2 antigen affinity purified polyclonal antibody (A08193-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PACS2 at approximately 130 kDa. The expected band size for PACS2 is at 98 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08193-1-pacs2-primary-antibodies-ihc-testing-2.jpgAnti-PACS2-Specific Antibody IHC analysis of PACS2 using anti-PACS2 antibody (A08193-1). PACS2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PACS2 Antibody (A08193-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08193-1-pacs2-primary-antibodies-ihc-testing-3.jpgAnti-PACS2-Specific Antibody IHC analysis of PACS2 using anti-PACS2 antibody (A08193-1). PACS2 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PACS2 Antibody (A08193-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08193-1-pacs2-primary-antibodies-ihc-testing-4.jpgAnti-PACS2-Specific Antibody IHC analysis of PACS2 using anti-PACS2 antibody (A08193-1). PACS2 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PACS2 Antibody (A08193-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08193-1-pacs2-primary-antibodies-ihc-testing-5.jpgAnti-PACS2-Specific Antibody IHC analysis of PACS2 using anti-PACS2 antibody (A08193-1). PACS2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PACS2 Antibody (A08193-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08193-1-pacs2-primary-antibodies-ihc-testing-6.jpgAnti-PACS2-Specific Antibody IHC analysis of PACS2 using anti-PACS2 antibody (A08193-1). PACS2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PACS2 Antibody (A08193-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08193-1-pacs2-primary-antibodies-ihc-testing-7.jpgAnti-PACS2-Specific Antibody IHC analysis of PACS2 using anti-PACS2 antibody (A08193-1). PACS2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PACS2 Antibody (A08193-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242292026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242302026-03-13T05:05:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01903-1-pcm1-primary-antibodies-wb-testing-1.jpgAnti-PCM1 Antibody Western blot analysis of PCM1 using anti-PCM1 antibody (A01903-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HT-1080 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCM1 antigen affinity purified polyclonal antibody (A01903-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PCM1 at approximately 280 kDa. The expected band size for PCM1 is at 229 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01903-1-pcm1-primary-antibodies-ihc-testing-2.jpgAnti-PCM1 Antibody IHC analysis of PCM1 using anti-PCM1 antibody (A01903-1). PCM1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PCM1 Antibody (A01903-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01903-1-pcm1-primary-antibodies-ihc-testing-3.jpgAnti-PCM1 Antibody IHC analysis of PCM1 using anti-PCM1 antibody (A01903-1). PCM1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PCM1 Antibody (A01903-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01903-1-pcm1-primary-antibodies-ihc-testing-4.jpgAnti-PCM1 Antibody IHC analysis of PCM1 using anti-PCM1 antibody (A01903-1). PCM1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PCM1 Antibody (A01903-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242312026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242322026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242332026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242342026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06382-1-pex16-primary-antibodies-wb-testing-1.jpgAnti-PEX16 Antibody Picoband®Western blot analysis of PEX16 using anti-PEX16 antibody (A06382-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PEX16 antigen affinity purified polyclonal antibody (A06382-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PEX16 at approximately 42 kDa. The expected band size for PEX16 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06382-1-pex16-primary-antibodies-if-testing-1.jpgAnti-PEX16 Antibody Picoband®IF analysis of PEX16 using anti-PEX16 antibody (A06382-1). PEX16 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PEX16 Antibody (A06382-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06382-1-pex16-primary-antibodies-ip-testing-1.jpgAnti-PEX16 Antibody Picoband®Immunoprecipitating PEX16 in MCF-7 whole cell lysate. Western blot analysis of PEX16 using anti-PEX16 antibody (A06382-1). Lane 1: MCF-7 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-PEX16 antibody in MCF-7 whole cell lysate, Lane 3: anti-PEX16 antibody (2μg) + MCF-7 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PEX16 antigen affinity purified polyclonal antibody (A06382-1) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for PEX16 at approximately 42 kDa. The expected band size for PEX16 is at 39 kDa. https://www.bosterbio.com/catalog/product/view/id/1242352026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02266-2-rora-primary-antibodies-wb-testing-1.jpgAnti-RORA Antibody Picoband®Western blot analysis of RORA using anti-RORA antibody (A02266-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RORA antigen affinity purified polyclonal antibody (A02266-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RORA at approximately 59 kDa. The expected band size for RORA is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02266-2-rora-primary-antibodies-if-testing-1.jpgAnti-RORA Antibody Picoband®IF analysis of RORA using anti-RORA antibody (A02266-2) and anti-Alpha Tubulin antibody (M03989-3). RORA was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RORA Antibody (A02266-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02266-2-rora-primary-antibodies-fcm-testing-1.jpgAnti-RORA Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-RORA antibody (A02266-2). Overlay histogram showing Jurkat cells stained with A02266-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RORA Antibody (A02266-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242362026-03-13T05:05:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02398-2-csnk2a1-primary-antibodies-wb-testing-1.jpgAnti-CSNK2A1 Antibody Western blot analysis of CSNK2A1 using anti-CSNK2A1 antibody (A02398-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat thymus tissue lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CSNK2A1 antigen affinity purified polyclonal antibody (A02398-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CSNK2A1 at approximately 40-45 kDa. The expected band size for CSNK2A1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02398-2-csnk2a1-primary-antibodies-ihc-testing-1.jpgAnti-CSNK2A1 AntibodyIHC analysis of CSNK2A1 using anti-CSNK2A1 antibody (A02398-2). CSNK2A1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CSNK2A1 Antibody (A02398-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242372026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242382026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11956-1-myl7-primary-antibodies-wb-testing-1.jpgAnti-MYL7 Antibody Picoband®Western blot analysis of MYL7 using anti-MYL7 antibody (A11956-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYL7 antigen affinity purified polyclonal antibody (A11956-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MYL7 at approximately 19 kDa. The expected band size for MYL7 is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11956-1-myl7-primary-antibodies-wb-testing-1_1.jpgAnti-MYL7 Antibody Picoband®Western blot analysis of MYL7 using anti-MYL7 antibody (A11956-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: rat lung tissue lysates, Lane 3: mouse heart tissue lysates, Lane 4: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYL7 antigen affinity purified polyclonal antibody (A11956-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MYL7 at approximately 19 kDa. The expected band size for MYL7 is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11956-1-myl7-primary-antibodies-ihc-testing-1.jpgAnti-MYL7 Antibody Picoband®IHC analysis of MYL7 using anti-MYL7 antibody (A11956-1). MYL7 was detected in a paraffin-embedded section of human heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYL7 Antibody (A11956-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11956-1-myl7-primary-antibodies-ihc-testing-2.jpgAnti-MYL7 Antibody Picoband®IHC analysis of MYL7 using anti-MYL7 antibody (A11956-1). MYL7 was detected in a paraffin-embedded section of human heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYL7 Antibody (A11956-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242392026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242402026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242412026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242422026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242432026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242442026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08012-1-pygb-primary-antibodies-wb-testing-1.jpgAnti-PYGB Antibody Picoband®Western blot analysis of PYGB using anti-PYGB antibody (A08012-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A375 whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PYGB antigen affinity purified polyclonal antibody (A08012-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PYGB at approximately 97 kDa. The expected band size for PYGB is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08012-1-pygb-primary-antibodies-ihc-testing-1.jpgAnti-PYGB Antibody Picoband®IHC analysis of PYGB using anti-PYGB antibody (A08012-1). PYGB was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PYGB Antibody (A08012-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08012-1-pygb-primary-antibodies-ihc-testing-2.jpgAnti-PYGB Antibody Picoband®IHC analysis of PYGB using anti-PYGB antibody (A08012-1). PYGB was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PYGB Antibody (A08012-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08012-1-pygb-primary-antibodies-ihc-testing-3.jpgAnti-PYGB Antibody Picoband®IHC analysis of PYGB using anti-PYGB antibody (A08012-1). PYGB was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PYGB Antibody (A08012-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242452026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242462026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242472026-03-16T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10315-1-sacm1l-primary-antibodies-ihc-testing-1.jpgAnti-SACM1L AntibodyIHC analysis of SACM1L using anti-SACM1L antibody (A10315-1). SACM1L was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-SACM1L Antibody (A10315-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10315-1-sacm1l-primary-antibodies-wb-testing-1.jpgAnti-SACM1L AntibodyWestern blot analysis of SACM1L using anti-SACM1L antibody (A10315-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat lung tissue lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse lung tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SACM1L antigen affinity purified polyclonal antibody (A10315-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SACM1L at approximately 67 kDa. The expected band size for SACM1L is at 67 kDa. https://www.bosterbio.com/catalog/product/view/id/1242492026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242502026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242512026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242532026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242542026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-ihc-testing-1.jpgAnti-COX17 Antibody Picoband® IHC analysis of COX17 using anti-COX17 antibody (A04584-1). COX17 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-COX17 Antibody (A04584-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-ihc-testing-2.jpgAnti-COX17 Antibody Picoband® IHC analysis of COX17 using anti-COX17 antibody (A04584-1). COX17 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-COX17 Antibody (A04584-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-ihc-testing-3.jpgAnti-COX17 Antibody Picoband® IHC analysis of COX17 using anti-COX17 antibody (A04584-1). COX17 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-COX17 Antibody (A04584-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-ihc-testing-4.jpgAnti-COX17 Antibody Picoband® IHC analysis of COX17 using anti-COX17 antibody (A04584-1). COX17 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-COX17 Antibody (A04584-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-wb-testing-1.jpgAnti-COX17 Antibody Picoband®Western blot analysis of COX17 using anti-COX17 antibody (A04584-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human LNCAP whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COX17 antigen affinity purified polyclonal antibody (A04584-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for COX17 at approximately 15 kDa. The expected band size for COX17 is at 7 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-ihc-testing-1_1.jpgAnti-COX17 Antibody Picoband®IHC analysis of COX17 using anti-COX17 antibody (A04584-1). COX17 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COX17 Antibody (A04584-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-ihc-testing-2_1.jpgAnti-COX17 Antibody Picoband®IHC analysis of COX17 using anti-COX17 antibody (A04584-1). COX17 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COX17 Antibody (A04584-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04584-1-cox17-primary-antibodies-if-testing-1.jpgAnti-COX17 Antibody Picoband®IF analysis of COX17 using anti-COX17 antibody (A04584-1). COX17 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-COX17 Antibody (A04584-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1242552026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242562026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242582026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242592026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242612026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02321-2-hexim1-primary-antibodies-wb-testing-1.jpgAnti-HEXIM1 Antibody Picoband®Western blot analysis of HEXIM1 using anti-HEXIM1 antibody (A02321-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: monkey COS-7 whole cell lysates, Lane 6: human LNCAP whole cell lysates, Lane 7: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HEXIM1 antigen affinity purified polyclonal antibody (A02321-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HEXIM1 at approximately 70 kDa. The expected band size for HEXIM1 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02321-2-hexim1-primary-antibodies-ihc-testing-1.jpgAnti-HEXIM1 Antibody Picoband®IHC analysis of HEXIM1 using anti-HEXIM1 antibody (A02321-2). HEXIM1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HEXIM1 Antibody (A02321-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02321-2-hexim1-primary-antibodies-ip-testing-1.jpgAnti-HEXIM1 Antibody Picoband®Immunoprecipitating (IP) HEXIM1 in Hela whole cell lysate. Western blot analysis of HEXIM1 using anti-HEXIM1 antibody (A02321-2); Lane 1: Hela whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-HEXIM1 antibody in Hela whole cell lysate; Lane 3: anti-HEXIM1 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-HEXIM1 antigen affinity purified polyclonal antibody (A02321-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light Chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for HEXIM1 at approximately 70 kDa. The expected band size for HEXIM1 is at 41 kDa. https://www.bosterbio.com/catalog/product/view/id/1242622026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242632026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242642026-03-16T05:08:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04811-1-larp7-primary-antibodies-wb-testing-1.jpgAnti-LARP7 Antibody Western blot analysis of LARP7 using anti-LARP7 antibody (A04811-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human THP-1 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LARP7 antigen affinity purified polyclonal antibody (A04811-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LARP7 at approximately 80 kDa. The expected band size for LARP7 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04811-1-larp7-primary-antibodies-ihc-testing-2.jpgAnti-LARP7 Antibody IHC analysis of LARP7 using anti-LARP7 antibody (A04811-1). LARP7 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LARP7 Antibody (A04811-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04811-1-larp7-primary-antibodies-ihc-testing-3.jpgAnti-LARP7 Antibody IHC analysis of LARP7 using anti-LARP7 antibody (A04811-1). LARP7 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LARP7 Antibody (A04811-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04811-1-larp7-primary-antibodies-ihc-testing-4.jpgAnti-LARP7 Antibody IHC analysis of LARP7 using anti-LARP7 antibody (A04811-1). LARP7 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LARP7 Antibody (A04811-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04811-1-larp7-primary-antibodies-if-testing-1.jpgAnti-LARP7 AntibodyIF analysis of LARP7 using anti-LARP7 antibody (A04811-1) and anti-Tubulin Alpha antibody (M03989-3). LARP7 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-LARP7 Antibody (A04811-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1242652026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04121-2-dhx58-primary-antibodies-wb-testing-1.jpgAnti-LGP2/DHX58 Antibody Picoband®Western blot analysis of DHX58 using anti-DHX58 antibody (A04121-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat kidney tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DHX58 antigen affinity purified polyclonal antibody (A04121-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DHX58 at approximately 77 kDa. The expected band size for DHX58 is at 77 kDa. https://www.bosterbio.com/catalog/product/view/id/1242662026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242672026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242682026-03-16T05:08:18+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242692026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242702026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242712026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01077-2-nr1d1-primary-antibodies-wb-testing-1.jpgAnti-NR1D1 Antibody Picoband® Western blot analysis of NR1D1 using anti-NR1D1 antibody (A01077-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat RH-35 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR1D1 antigen affinity purified polyclonal antibody (A01077-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NR1D1 at approximately 67 kDa. The expected band size for NR1D1 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01077-2-nr1d1-primary-antibodies-wb-testing-1_1.jpgAnti-NR1D1 Antibody Picoband®Western blot analysis of NR1D1 using anti-NR1D1 antibody (A01077-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR1D1 antigen affinity purified polyclonal antibody (A01077-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NR1D1 at approximately 67 kDa. The expected band size for NR1D1 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01077-2-nr1d1-primary-antibodies-ihc-testing-1.jpgAnti-NR1D1 Antibody Picoband®IHC analysis of NR1D1 using anti-NR1D1 antibody (A01077-2). NR1D1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR1D1 Antibody (A01077-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01077-2-nr1d1-primary-antibodies-ihc-testing-2.jpgAnti-NR1D1 Antibody Picoband®IHC analysis of NR1D1 using anti-NR1D1 antibody (A01077-2). NR1D1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR1D1 Antibody (A01077-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01077-2-nr1d1-primary-antibodies-ihc-testing-3.jpgAnti-NR1D1 Antibody Picoband®IHC analysis of NR1D1 using anti-NR1D1 antibody (A01077-2). NR1D1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR1D1 Antibody (A01077-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01077-2-nr1d1-primary-antibodies-fcm-testing-1.jpgAnti-NR1D1 Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-NR1D1 antibody (A01077-2). Overlay histogram showing U251 cells stained with A01077-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NR1D1 Antibody (A01077-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242722026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242732026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242742026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-wb-testing-1.jpgAnti-PHF5A Antibody Picoband®Western blot analysis of PHF5A using anti-PHF5A antibody (A10060). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF5A antigen affinity purified polyclonal antibody (A10060) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PHF5A at approximately 14 kDa. The expected band size for PHF5A is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-ihc-testing-1.jpgAnti-PHF5A Antibody Picoband®IHC analysis of PHF5A using anti-PHF5A antibody (A10060). PHF5A was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF5A Antibody (A10060) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-ihc-testing-2.jpgAnti-PHF5A Antibody Picoband®IHC analysis of PHF5A using anti-PHF5A antibody (A10060). PHF5A was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF5A Antibody (A10060) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-ihc-testing-3.jpgAnti-PHF5A Antibody Picoband®IHC analysis of PHF5A using anti-PHF5A antibody (A10060). PHF5A was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF5A Antibody (A10060) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-ihc-testing-4.jpgAnti-PHF5A Antibody Picoband®IHC analysis of PHF5A using anti-PHF5A antibody (A10060). PHF5A was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF5A Antibody (A10060) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-if-testing-1.jpgAnti-PHF5A Antibody Picoband®IF analysis of PHF5A using anti-PHF5A antibody (A10060). PHF5A was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PHF5A Antibody (A10060) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-if-testing-2.jpgAnti-PHF5A Antibody Picoband®IF analysis of PHF5A using anti-PHF5A antibody (A10060) and anti-Alpha Tubulin antibody (M03989-3). PHF5A was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PHF5A Antibody (A10060) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10060-phf5a-primary-antibodies-ip-testing-1.jpgAnti-PHF5A Antibody Picoband®Immunoprecipitating PHF5A in Hela whole cell lysate. Western blot analysis of PHF5A using anti-PHF5A antibody (A10060). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-PHF5A antibody in Hela whole cell lysate, Lane 3: anti-PHF5A antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PHF5A antigen affinity purified polyclonal antibody (A10060) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for PHF5A at approximately 14 kDa. The expected band size for PHF5A is at 12 kDa. https://www.bosterbio.com/catalog/product/view/id/1242752026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242762026-03-16T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06592-1-pik3ip1-primary-antibodies-wb-testing-1.jpgAnti-PIK3IP1 Antibody Western blot analysis of PIK3IP1 using anti-PIK3IP1 antibody (A06592-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIK3IP1 antigen affinity purified polyclonal antibody (A06592-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PIK3IP1 at approximately 31 kDa. The expected band size for PIK3IP1 is at 28 kDa. https://www.bosterbio.com/catalog/product/view/id/1242772026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03720-2-pold1-primary-antibodies-wb-testing-1.jpgAnti-POLD1 Antibody Picoband®Western blot analysis of POLD1 using anti-POLD1 antibody (A03720-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat spleen tissue lysates, Lane 7: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLD1 antigen affinity purified polyclonal antibody (A03720-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for POLD1 at approximately 124 kDa. The expected band size for POLD1 is at 124 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03720-2-pold1-primary-antibodies-ihc-testing-1.jpgAnti-POLD1 Antibody Picoband®IHC analysis of POLD1 using anti-POLD1 antibody (A03720-2). POLD1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POLD1 Antibody (A03720-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03720-2-pold1-primary-antibodies-if-testing-1.jpgAnti-POLD1 Antibody Picoband®IF analysis of POLD1 using anti-POLD1 antibody (A03720-2) and anti-Beta Tubulin antibody (M01857-3). POLD1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POLD1 Antibody (A03720-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03720-2-pold1-primary-antibodies-ip-testing-1.jpgAnti-POLD1 Antibody Picoband®Immunoprecipitating POLD1 in 293T whole cell lysate. Western blot analysis of POLD1 using anti-POLD1 antibody (A03720-2). Lane 1: 293T whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-POLD1 antibody in 293T whole cell lysate, Lane 3: anti-POLD1 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-POLD1 antigen affinity purified polyclonal antibody (A03720-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for POLD1 at approximately 124 kDa. The expected band size for POLD1 is at 124 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03720-2-pold1-primary-antibodies-fcm-testing-1.jpgAnti-POLD1 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-POLD1 antibody (A03720-2). Overlay histogram showing 293T cells stained with A03720-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POLD1 Antibody (A03720-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242782026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242792026-03-16T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06007-2-rab2-rab2a-primary-antibodies-wb-testing-1.jpgAnti-RAB2/RAB2A Antibody Western blot analysis of RAB2/RAB2A using anti-RAB2/RAB2A antibody (A06007-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB2/RAB2A antigen affinity purified polyclonal antibody (A06007-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RAB2/RAB2A at approximately 20 kDa. The expected band size for RAB2/RAB2A is at 20, 24 kDa. https://www.bosterbio.com/catalog/product/view/id/1242802026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07894-1-sesn3-primary-antibodies-wb-testing-1.jpgAnti-SESN3 Antibody Picoband®Western blot analysis of SESN3 using anti-SESN3 antibody (A07894-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat ovary tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SESN3 antigen affinity purified polyclonal antibody (A07894-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SESN3 at approximately 59 kDa. The expected band size for SESN3 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07894-1-sesn3-primary-antibodies-if-testing-1.jpgAnti-SESN3 Antibody Picoband®IF analysis of SESN3 using anti-SESN3 antibody (A07894-1) and anti-Beta Tubulin antibody (M01857-3). SESN3 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SESN3 Antibody (A07894-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07894-1-sesn3-primary-antibodies-fcm-testing-1.jpgAnti-SESN3 Antibody Picoband®Flow Cytometry analysis of A549 cells using anti-SESN3 antibody (A07894-1). Overlay histogram showing A549 cells stained with A07894-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SESN3 Antibody (A07894-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242812026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242822026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242832026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01863-1-serpine2-primary-antibodies-wb-testing-1.jpgAnti-SERPINE2 Antibody Picoband®Western blot analysis of SERPINE2 using anti-SERPINE2 antibody (A01863-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SIHA whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SERPINE2 antigen affinity purified polyclonal antibody (A01863-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SERPINE2 at approximately 44 kDa. The expected band size for SERPINE2 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01863-1-serpine2-primary-antibodies-ihc-testing-1.jpgAnti-SERPINE2 Antibody Picoband®IHC analysis of SERPINE2 using anti-SERPINE2 antibody (A01863-1). SERPINE2 was detected in a paraffin-embedded section of human adrenal pheochromocytoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SERPINE2 Antibody (A01863-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01863-1-serpine2-primary-antibodies-ihc-testing-2.jpgAnti-SERPINE2 Antibody Picoband®IHC analysis of SERPINE2 using anti-SERPINE2 antibody (A01863-1). SERPINE2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SERPINE2 Antibody (A01863-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01863-1-serpine2-primary-antibodies-fcm-testing-1.jpgAnti-SERPINE2 Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-SERPINE2 antibody (A01863-1). Overlay histogram showing U251 cells stained with A01863-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SERPINE2 Antibody (A01863-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242842026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01780-2-foxc2-primary-antibodies-wb-testing-1.jpgAnti-FOXC2 Picoband® AntibodyWestern blot analysis of FOXC2 using anti-FOXC2 antibody (A01780-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A375 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse C2C12 whole cell lysates, Lane 8: mouse 3T3-L1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXC2 antigen affinity purified polyclonal antibody (A01780-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOXC2 at approximately 60 kDa. The expected band size for FOXC2 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01780-2-foxc2-primary-antibodies-if-testing-1.jpgAnti-FOXC2 Picoband® AntibodyIF analysis of FOXC2 using anti-FOXC2 antibody (A01780-2) and anti-Tubulin Alpha antibody (M03989-3). FOXC2 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-FOXC2 Antibody (A01780-2) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01780-2-foxc2-primary-antibodies-fcm-testing-1.jpgAnti-FOXC2 Picoband® AntibodyFlow Cytometry analysis of Hela cells using anti-FOXC2 antibody (A01780-2). Overlay histogram showing Hela cells stained with A01780-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FOXC2 Antibody (A01780-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1242852026-03-16T05:08:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11634-1-mrpl23-primary-antibodies-wb-testing-1.jpgAnti-MRPL23 AntibodyWestern blot analysis of MRPL23 using anti-MRPL23 antibody (A11634-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human A2780 whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human THP-1 whole cell lysates, Lane 7: human SH-SY5Y whole cell lysates, Lane 8: human A549 tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MRPL23 antigen affinity purified polyclonal antibody (A11634-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MRPL23 at approximately 18 kDa. The expected band size for MRPL23 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11634-1-mrpl23-primary-antibodies-ihc-testing-1.jpgAnti-MRPL23 AntibodyIHC analysis of MRPL23 using anti-MRPL23 antibody (A11634-1). MRPL23 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MRPL23 Antibody (A11634-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11634-1-mrpl23-primary-antibodies-ihc-testing-2.jpgAnti-MRPL23 AntibodyIHC analysis of MRPL23 using anti-MRPL23 antibody (A11634-1). MRPL23 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MRPL23 Antibody (A11634-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242862026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242872026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242882026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03290-1-dnajb6-primary-antibodies-wb-testing-1.jpgAnti-DNAJB6 Antibody Picoband® Western blot analysis of DNAJB6 using anti-DNAJB6 antibody (A03290-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJB6 antigen affinity purified polyclonal antibody (A03290-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNAJB6 at approximately 27 kDa. The expected band size for DNAJB6 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03290-1-dnajb6-primary-antibodies-ihc-testing-2.jpgAnti-DNAJB6 Antibody Picoband® IHC analysis of DNAJB6 using anti-DNAJB6 antibody (A03290-1). DNAJB6 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNAJB6 Antibody (A03290-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242892026-03-13T05:05:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00147-1-hbb-primary-antibodies-wb-testing-1.jpgAnti-HBB Antibody Western blot analysis of HBB using anti-HBB antibody (A00147-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: rat lung tissue lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HBB antigen affinity purified polyclonal antibody (A00147-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HBB at approximately 13 kDa. The expected band size for HBB is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00147-1-hbb-primary-antibodies-ihc-testing-2.jpgAnti-HBB Antibody IHC analysis of HBB using anti-HBB antibody (A00147-1). HBB was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HBB Antibody (A00147-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00147-1-hbb-primary-antibodies-ihc-testing-3.jpgAnti-HBB Antibody IHC analysis of HBB using anti-HBB antibody (A00147-1). HBB was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HBB Antibody (A00147-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242902026-03-13T05:05:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02125-1-dhcr24-primary-antibodies-wb-testing-1.jpgAnti-DHCR24 Antibody Western blot analysis of DHCR24 using anti-DHCR24 antibody (A02125-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DHCR24 antigen affinity purified polyclonal antibody (A02125-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DHCR24 at approximately 60 kDa. The expected band size for DHCR24 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02125-1-dhcr24-primary-antibodies-ihc-testing-2.jpgAnti-DHCR24 Antibody IHC analysis of DHCR24 using anti-DHCR24 antibody (A02125-1). DHCR24 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-DHCR24 Antibody (A02125-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242912026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242922026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242932026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242942026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242952026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03871-2-gpc1-primary-antibodies-wb-testing-1.jpgAnti-Glypican 1/GPC1 Antibody Picoband®Western blot analysis of Glypican 1/GPC1 using anti-Glypican 1/GPC1 antibody (A03871-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Glypican 1/GPC1 antigen affinity purified polyclonal antibody (A03871-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Glypican 1/GPC1 at approximately 62 kDa. The expected band size for Glypican 1/GPC1 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03871-2-gpc1-primary-antibodies-ihc-testing-1.jpgAnti-Glypican 1/GPC1 Antibody Picoband®IHC analysis of Glypican 1/GPC1 using anti-Glypican 1/GPC1 antibody (A03871-2). Glypican 1/GPC1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Glypican 1/GPC1 Antibody (A03871-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03871-2-gpc1-primary-antibodies-ihc-testing-2.jpgAnti-Glypican 1/GPC1 Antibody Picoband®IHC analysis of Glypican 1/GPC1 using anti-Glypican 1/GPC1 antibody (A03871-2). Glypican 1/GPC1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Glypican 1/GPC1 Antibody (A03871-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1242962026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242972026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242982026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1242992026-03-16T05:08:19+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243002026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-2-pfkp-primary-antibodies-wb-testing-1.jpgAnti-PFKP Antibody Western blot analysis of PFKP using anti-PFKP antibody (A07337-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates, Lane 7: mouse ANA-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PFKP antigen affinity purified polyclonal antibody (A07337-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PFKP at approximately 86 kDa. The expected band size for PFKP is at 86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-2-pfkp-primary-antibodies-ihc-testing-2.jpgAnti-PFKP Antibody IHC analysis of PFKP using anti-PFKP antibody (A07337-2). PFKP was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PFKP Antibody (A07337-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-2-pfkp-primary-antibodies-ihc-testing-3.jpgAnti-PFKP Antibody IHC analysis of PFKP using anti-PFKP antibody (A07337-2). PFKP was detected in a paraffin-embedded section of human uterine tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PFKP Antibody (A07337-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-2-pfkp-primary-antibodies-ihc-testing-4.jpgAnti-PFKP Antibody IHC analysis of PFKP using anti-PFKP antibody (A07337-2). PFKP was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PFKP Antibody (A07337-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-2-pfkp-primary-antibodies-ihc-testing-5.jpgAnti-PFKP Antibody IHC analysis of PFKP using anti-PFKP antibody (A07337-2). PFKP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-PFKP Antibody (A07337-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-2-pfkp-primary-antibodies-if-testing-1.jpgAnti-PFKP AntibodyIF analysis of PFKP using anti-PFKP antibody (A07337-2). PFKP was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-PFKP Antibody (A07337-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-pgd-picoband-trade-antibody-a01623-3-boster.html2026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01623-3-pgd-primary-antibodies-wb-testing-1.jpgAnti-PGD Antibody Picoband® Western blot analysis of PGD using anti-PGD antibody (A01623-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGD antigen affinity purified polyclonal antibody (Catalog # A01623-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGD at approximately 48 kDa. The expected band size for PGD is at 54,48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01623-3-pgd-primary-antibodies-if-testing-2.jpgAnti-PGD Antibody Picoband® IF analysis of PGD using anti-PGD antibody (A01623-3). PGD was detected in an immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PGD Antibody (A01623-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01623-3-pgd-primary-antibodies-fcm-testing-3.pngAnti-PGD Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PGD antibody (A01623-3). Overlay histogram showing HepG2 cells stained with A01623-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PGD Antibody (A01623-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1243022026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-sec61g-picoband-trade-antibody-a12389-boster.html2026-03-17T05:15:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12389-sec61g-primary-antibodies-wb-testing-1.jpgAnti-SEC61G Antibody Picoband® Western blot analysis of SEC61G using anti-SEC61G antibody (A12389). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human U87 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SEC61G antigen affinity purified polyclonal antibody (Catalog # A12389) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SEC61G at approximately 12 kDa. The expected band size for SEC61G is at 8 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12389-sec61g-primary-antibodies-ihc-testing-2.jpgAnti-SEC61G Antibody Picoband® IHC analysis of SEC61G using anti-SEC61G antibody (A12389). SEC61G was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SEC61G Antibody (A12389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12389-sec61g-primary-antibodies-ihc-testing-3.jpgAnti-SEC61G Antibody Picoband® IHC analysis of SEC61G using anti-SEC61G antibody (A12389). SEC61G was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SEC61G Antibody (A12389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12389-sec61g-primary-antibodies-ihc-testing-4.jpgAnti-SEC61G Antibody Picoband® IHC analysis of SEC61G using anti-SEC61G antibody (A12389). SEC61G was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SEC61G Antibody (A12389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12389-sec61g-primary-antibodies-ihc-testing-5.jpgAnti-SEC61G Antibody Picoband® IHC analysis of SEC61G using anti-SEC61G antibody (A12389). SEC61G was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SEC61G Antibody (A12389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12389-sec61g-primary-antibodies-ihc-testing-6.jpgAnti-SEC61G Antibody Picoband® IHC analysis of SEC61G using anti-SEC61G antibody (A12389). SEC61G was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SEC61G Antibody (A12389) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1243042026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243052026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243062026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07010-2-coro1c-primary-antibodies-wb-testing-1_1.jpgAnti-CORO1C Antibody Picoband®Western blot analysis of CORO1C using anti-CORO1C antibody (A07010-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CORO1C antigen affinity purified polyclonal antibody (A07010-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CORO1C at approximately 53 kDa. The expected band size for CORO1C is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07010-2-coro1c-primary-antibodies-wb-testing-2.jpgAnti-CORO1C Antibody Picoband®Western blot analysis of CORO1C using anti-CORO1C antibody (A07010-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CORO1C antigen affinity purified polyclonal antibody (A07010-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CORO1C at approximately 53 kDa. The expected band size for CORO1C is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07010-2-coro1c-primary-antibodies-ihc-testing-1.jpgAnti-CORO1C Antibody Picoband®IHC analysis of CORO1C using anti-CORO1C antibody (A07010-2). CORO1C was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CORO1C Antibody (A07010-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07010-2-coro1c-primary-antibodies-ihc-testing-2_1.jpgAnti-CORO1C Antibody Picoband®IHC analysis of CORO1C using anti-CORO1C antibody (A07010-2). CORO1C was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CORO1C Antibody (A07010-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07010-2-coro1c-primary-antibodies-ihc-testing-3.jpgAnti-CORO1C Antibody Picoband®IHC analysis of CORO1C using anti-CORO1C antibody (A07010-2). CORO1C was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CORO1C Antibody (A07010-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07010-2-coro1c-primary-antibodies-ip-testing-1.jpgAnti-CORO1C Antibody Picoband®Immunoprecipitating CORO1C in A549 whole cell lysate. Western blot analysis of CORO1C using anti-CORO1C antibody (A07010-2). Lane 1: A549 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-CORO1C antibody in A549 whole cell lysate, Lane 3: anti-CORO1C antibody (2μg) + A549 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CORO1C antigen affinity purified polyclonal antibody (A07010-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for CORO1C at approximately 53 kDa. The expected band size for CORO1C is at 53 kDa. https://www.bosterbio.com/catalog/product/view/id/1243072026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243082026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243092026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243102026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04923-2-dhx36-primary-antibodies-wb-testing-1.jpgAnti-DHX36 Antibody Picoband®Western blot analysis of DHX36 using anti-DHX36 antibody (A04923-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DHX36 antigen affinity purified polyclonal antibody (A04923-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DHX36 at approximately 110 kDa. The expected band size for DHX36 is at 115 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04923-2-dhx36-primary-antibodies-if-testing-1.jpgAnti-DHX36 Antibody Picoband®IF analysis of DHX36 using anti-DHX36 antibody (A04923-2) and anti-Alpha Tubulin antibody (M03989-3). DHX36 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DHX36 Antibody (A04923-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04923-2-dhx36-primary-antibodies-fcm-testing-1.jpgAnti-DHX36 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-DHX36 antibody (A04923-2). Overlay histogram showing 293T cells stained with A04923-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DHX36 Antibody (A04923-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243112026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02249-2-dio2-primary-antibodies-wb-testing-1.jpgAnti-DIO2 Antibody Picoband® Western blot analysis of DIO2 using anti-DIO2 antibody (A02249-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DIO2 antigen affinity purified polyclonal antibody (A02249-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DIO2 at approximately 32 kDa. The expected band size for DIO2 is at 31 kDa. https://www.bosterbio.com/catalog/product/view/id/1243122026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243132026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243142026-03-13T05:05:03+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243152026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243162026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08971-2-trim11-primary-antibodies-wb-testing-1.jpgAnti-TRIM11 Antibody Picoband®Western blot analysis of TRIM11 using anti-TRIM11 antibody (A08971-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIM11 antigen affinity purified polyclonal antibody (A08971-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIM11 at approximately 53 kDa. The expected band size for TRIM11 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08971-2-trim11-primary-antibodies-if-testing-1.jpgAnti-TRIM11 Antibody Picoband®IF analysis of TRIM11 using anti-TRIM11 antibody (A08971-2) and anti-Alpha Tubulin antibody (M03989-3). TRIM11 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TRIM11 Antibody (A08971-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08971-2-trim11-primary-antibodies-fcm-testing-1.jpgAnti-TRIM11 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-TRIM11 antibody (A08971-2). Overlay histogram showing MCF-7 cells stained with A08971-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TRIM11 Antibody (A08971-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243172026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243182026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03042-3-usp14-primary-antibodies-wb-testing-1.jpgAnti-USP14 Antibody Picoband®Western blot analysis of USP14 using anti-USP14 antibody (A03042-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human SK-OV-3 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-USP14 antigen affinity purified polyclonal antibody (A03042-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for USP14 at approximately 60 kDa. The expected band size for USP14 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03042-3-usp14-primary-antibodies-fcm-testing-1.jpgAnti-USP14 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-USP14 antibody (A03042-3). Overlay histogram showing Jurkat cells stained with A03042-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-USP14 Antibody (A03042-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243192026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243202026-03-16T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06922-1-usp39-primary-antibodies-wb-testing-1.jpgAnti-USP39 AntibodyWestern blot analysis of USP39 using anti-USP39 antibody (A06922-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-USP39 antigen affinity purified polyclonal antibody (A06922-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for USP39 at approximately 60 kDa. The expected band size for USP39 is at 65 kDa. https://www.bosterbio.com/catalog/product/view/id/1243212026-03-16T05:08:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09572-1-cox6a1-primary-antibodies-wb-testing-1.jpgAnti-COX6A1 Antibody Western blot analysis of COX6A1 using anti-COX6A1 antibody (A09572-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COX6A1 antigen affinity purified polyclonal antibody (A09572-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for COX6A1 at approximately 14 kDa. The expected band size for COX6A1 is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09572-1-cox6a1-primary-antibodies-ihc-testing-1.jpgAnti-COX6A1 AntibodyIHC analysis of COX6A1 using anti-COX6A1 antibody (A09572-1). COX6A1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COX6A1 Antibody (A09572-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09572-1-cox6a1-primary-antibodies-ihc-testing-2.jpgAnti-COX6A1 AntibodyIHC analysis of COX6A1 using anti-COX6A1 antibody (A09572-1). COX6A1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COX6A1 Antibody (A09572-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1243222026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243232026-03-13T05:05:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01656-ddx17-primary-antibodies-wb-testing-1.jpgAnti-DDX17 Antibody Western blot analysis of DDX17 using anti-DDX17 antibody (A01656). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DDX17 antigen affinity purified polyclonal antibody (A01656) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DDX17 at approximately 70-80 kDa. The expected band size for DDX17 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01656-ddx17-primary-antibodies-ihc-testing-1.jpgAnti-DDX17 AntibodyIHC analysis of DDX17 using anti-DDX17 antibody (A01656). DDX17 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX17 Antibody (A01656) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01656-ddx17-primary-antibodies-ihc-testing-2.jpgAnti-DDX17 AntibodyIHC analysis of DDX17 using anti-DDX17 antibody (A01656). DDX17 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX17 Antibody (A01656) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1243242026-03-16T05:08:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243252026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-wb-testing-1.jpgAnti-RPS12 Antibody Picoband® Western blot analysis of RPS12 using anti-RPS12 antibody (A01040-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS12 antigen affinity purified polyclonal antibody (A01040-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPS12 at approximately 15 kDa. The expected band size for RPS12 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-2.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-3.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-4.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-5.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-6.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-7.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-8.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-9.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-10.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-11.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-12.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-13.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human clear cell renal cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-14.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-15.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-16.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-17.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-18.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-19.jpgAnti-RPS12 Antibody Picoband® IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-wb-testing-1_1.jpgAnti-RPS12 Antibody Picoband®Western blot analysis of RPS12 using anti-RPS12 antibody (A01040-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse Raw264.7 whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS12 antigen affinity purified polyclonal antibody (A01040-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPS12 at approximately 15 kDa. The expected band size for RPS12 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-1.jpgAnti-RPS12 Antibody Picoband®IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-2_1.jpgAnti-RPS12 Antibody Picoband®IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-3_1.jpgAnti-RPS12 Antibody Picoband®IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-4_1.jpgAnti-RPS12 Antibody Picoband®IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-ihc-testing-5_1.jpgAnti-RPS12 Antibody Picoband®IHC analysis of RPS12 using anti-RPS12 antibody (A01040-3). RPS12 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPS12 Antibody (A01040-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01040-3-rps12-primary-antibodies-fcm-testing-1.jpgAnti-RPS12 Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-RPS12 antibody (A01040-3). Overlay histogram showing MCF-7 cells stained with A01040-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPS12 Antibody (A01040-3, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243262026-03-16T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06454-rps26-primary-antibodies-wb-testing-1.jpgAnti-RPS26 Antibody Western blot analysis of RPS26 using anti-RPS26 antibody (A06454). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat ovary tissue lysates, Lane 7: mouse lung tissue lysates, Lane 8: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS26 antigen affinity purified polyclonal antibody (A06454) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPS26 at approximately 18 kDa. The expected band size for RPS26 is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06454-rps26-primary-antibodies-ihc-testing-1.jpgAnti-RPS26 AntibodyIHC analysis of RPS26 using anti-RPS26 antibody (A06454). RPS26 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPS26 Antibody (A06454) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1243272026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243282026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243292026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13448-1-dnajb12-primary-antibodies-wb-testing-1.jpgAnti-DNAJB12 Antibody Picoband®Western blot analysis of DNAJB12 using anti-DNAJB12 antibody (A13448-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJB12 antigen affinity purified polyclonal antibody (A13448-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNAJB12 at approximately 42 kDa. The expected band size for DNAJB12 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13448-1-dnajb12-primary-antibodies-ihc-testing-1.jpgAnti-DNAJB12 Antibody Picoband®IHC analysis of DNAJB12 using anti-DNAJB12 antibody (A13448-1). DNAJB12 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNAJB12 Antibody (A13448-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13448-1-dnajb12-primary-antibodies-ihc-testing-2.jpgAnti-DNAJB12 Antibody Picoband®IHC analysis of DNAJB12 using anti-DNAJB12 antibody (A13448-1). DNAJB12 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNAJB12 Antibody (A13448-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13448-1-dnajb12-primary-antibodies-ihc-testing-3.jpgAnti-DNAJB12 Antibody Picoband®IHC analysis of DNAJB12 using anti-DNAJB12 antibody (A13448-1). DNAJB12 was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DNAJB12 Antibody (A13448-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13448-1-dnajb12-primary-antibodies-if-testing-1.jpgAnti-DNAJB12 Antibody Picoband®IF analysis of DNAJB12 using anti-DNAJB12 antibody (A13448-1). DNAJB12 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DNAJB12 Antibody (A13448-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13448-1-dnajb12-primary-antibodies-fcm-testing-1.jpgAnti-DNAJB12 Antibody Picoband®Flow Cytometry analysis of A431 cells using anti-DNAJB12 antibody (A13448-1). Overlay histogram showing A431 cells stained with A13448-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DNAJB12 Antibody (A13448-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13448-1-dnajb12-primary-antibodies-fcm-testing-2.jpgAnti-DNAJB12 Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-DNAJB12 antibody (A13448-1). Overlay histogram showing U251 cells stained with A13448-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DNAJB12 Antibody (A13448-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243302026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04013-3-elac2-primary-antibodies-wb-testing-1.jpgAnti-ELAC2 Antibody Picoband®Western blot analysis of ELAC2 using anti-ELAC2 antibody (A04013-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ELAC2 antigen affinity purified polyclonal antibody (A04013-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ELAC2 at approximately 92 kDa. The expected band size for ELAC2 is at 92 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04013-3-elac2-primary-antibodies-ihc-testing-1.jpgAnti-ELAC2 Antibody Picoband®IHC analysis of ELAC2 using anti-ELAC2 antibody (A04013-3). ELAC2 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ELAC2 Antibody (A04013-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04013-3-elac2-primary-antibodies-ihc-testing-2.jpgAnti-ELAC2 Antibody Picoband®IHC analysis of ELAC2 using anti-ELAC2 antibody (A04013-3). ELAC2 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ELAC2 Antibody (A04013-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04013-3-elac2-primary-antibodies-if-testing-1.jpgAnti-ELAC2 Antibody Picoband®IF analysis of ELAC2 using anti-ELAC2 antibody (A04013-3) and anti-Alpha Tubulin antibody (M03989-3). ELAC2 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ELAC2 Antibody (A04013-3) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04013-3-elac2-primary-antibodies-ip-testing-1.jpgAnti-ELAC2 Antibody Picoband®Immunoprecipitating ELAC2 in HepG2 whole cell lysate. Western blot analysis of ELAC2 using anti-ELAC2 antibody (A04013-3). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-ELAC2 antibody in HepG2 whole cell lysate, Lane 3: anti-ELAC2 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ELAC2 antigen affinity purified polyclonal antibody (A04013-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ELAC2 at approximately 92 kDa. The expected band size for ELAC2 is at 92 kDa. https://www.bosterbio.com/catalog/product/view/id/1243312026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-wb-testing-1.jpgAnti-ETFB Antibody Picoband®Western blot analysis of ETFB using anti-ETFB antibody (A05431-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat heart tissue lysates, Lane 4: rat skeletal muscle tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse skeletal muscle tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ETFB antigen affinity purified polyclonal antibody (A05431-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ETFB at approximately 28 kDa. The expected band size for ETFB is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-ihc-testing-1.jpgAnti-ETFB Antibody Picoband®IHC analysis of ETFB using anti-ETFB antibody (A05431-1). ETFB was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ETFB Antibody (A05431-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-ihc-testing-2.jpgAnti-ETFB Antibody Picoband®IHC analysis of ETFB using anti-ETFB antibody (A05431-1). ETFB was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ETFB Antibody (A05431-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-ihc-testing-3.jpgAnti-ETFB Antibody Picoband®IHC analysis of ETFB using anti-ETFB antibody (A05431-1). ETFB was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ETFB Antibody (A05431-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-ihc-testing-4.jpgAnti-ETFB Antibody Picoband®IHC analysis of ETFB using anti-ETFB antibody (A05431-1). ETFB was detected in a paraffin-embedded section of mouse adrenal tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ETFB Antibody (A05431-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-ihc-testing-5.jpgAnti-ETFB Antibody Picoband®IHC analysis of ETFB using anti-ETFB antibody (A05431-1). ETFB was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ETFB Antibody (A05431-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-if-testing-1.jpgAnti-ETFB Antibody Picoband®IF analysis of ETFB using anti-ETFB antibody (A05431-1). ETFB was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ETFB Antibody (A05431-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05431-1-etfb-primary-antibodies-ip-testing-1.jpgAnti-ETFB Antibody Picoband®Immunoprecipitating ETFB in HepG2 whole cell lysate. Western blot analysis of ETFB using anti-ETFB antibody (A05431-1). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-ETFB antibody in HepG2 whole cell lysate, Lane 3: anti-ETFB antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ETFB antigen affinity purified polyclonal antibody (A05431-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for ETFB at approximately 28 kDa. The expected band size for ETFB is at 28 kDa. https://www.bosterbio.com/catalog/product/view/id/1243322026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243332026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243342026-03-16T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04618-1-gars-gars1-primary-antibodies-wb-testing-1.jpgAnti-GARS/GARS1 Antibody Western blot analysis of GARS/GARS1 using anti-GARS/GARS1 antibody (A04618-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human HT-1080 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GARS/GARS1 antigen affinity purified polyclonal antibody (A04618-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GARS/GARS1 at approximately 80 kDa. The expected band size for GARS/GARS1 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04618-1-gars-gars1-primary-antibodies-ihc-testing-2.jpgAnti-GARS/GARS1 Antibody IHC analysis of GARS/GARS1 using anti-GARS/GARS1 antibody (A04618-1). GARS/GARS1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-GARS/GARS1 Antibody (A04618-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04618-1-gars-gars1-primary-antibodies-ihc-testing-3.jpgAnti-GARS/GARS1 Antibody IHC analysis of GARS/GARS1 using anti-GARS/GARS1 antibody (A04618-1). GARS/GARS1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-GARS/GARS1 Antibody (A04618-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1243352026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243362026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243372026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243382026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243402026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243412026-03-16T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12904-2-krt80-primary-antibodies-wb-testing-1.jpgAnti-KRT80 AntibodyWestern blot analysis of KRT80 using anti-KRT80 antibody (A12904-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KRT80 antigen affinity purified polyclonal antibody (A12904-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KRT80 at approximately 47,50 kDa. The expected band size for KRT80 is at 47 kDa. https://www.bosterbio.com/catalog/product/view/id/1243422026-03-16T05:08:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07554-lars2-primary-antibodies-wb-testing-1_1.jpgAnti-LARS2 Antibody Picoband®Western blot analysis of LARS2 using anti-LARS2 antibody (A07554). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LARS2 antigen affinity purified polyclonal antibody (A07554) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LARS2 at approximately 102 kDa. The expected band size for LARS2 is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07554-lars2-primary-antibodies-ihc-testing-1_1.jpgAnti-LARS2 Antibody Picoband®IHC analysis of LARS2 using anti-LARS2 antibody (A07554). LARS2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LARS2 Antibody (A07554) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07554-lars2-primary-antibodies-ihc-testing-2_1.jpgAnti-LARS2 Antibody Picoband®IHC analysis of LARS2 using anti-LARS2 antibody (A07554). LARS2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LARS2 Antibody (A07554) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07554-lars2-primary-antibodies-ihc-testing-3_1.jpgAnti-LARS2 Antibody Picoband®IHC analysis of LARS2 using anti-LARS2 antibody (A07554). LARS2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LARS2 Antibody (A07554) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07554-lars2-primary-antibodies-ihc-testing-4_1.jpgAnti-LARS2 Antibody Picoband®IHC analysis of LARS2 using anti-LARS2 antibody (A07554). LARS2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LARS2 Antibody (A07554) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07554-lars2-primary-antibodies-ihc-testing-5_1.jpgAnti-LARS2 Antibody Picoband®IHC analysis of LARS2 using anti-LARS2 antibody (A07554). LARS2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LARS2 Antibody (A07554) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07554-lars2-primary-antibodies-if-testing-1.jpgAnti-LARS2 Antibody Picoband®IF analysis of LARS2 using anti-LARS2 antibody (A07554). LARS2 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LARS2 Antibody (A07554) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1243432026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243442026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243452026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08029-1-mpc2-primary-antibodies-wb-testing-1.jpgAnti-MPC2 Antibody Picoband®Western blot analysis of MPC2 using anti-MPC2 antibody (A08029-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat kidney tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPC2 antigen affinity purified polyclonal antibody (A08029-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MPC2 at approximately 14 kDa. The expected band size for MPC2 is at 14 kDa. https://www.bosterbio.com/catalog/product/view/id/1243462026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243472026-03-16T05:08:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243482026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02898-2-msi2-primary-antibodies-wb-testing-1.jpgAnti-MSI2 Antibody Picoband®Western blot analysis of MSI2 using anti-MSI2 antibody (A02898-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MSI2 antigen affinity purified polyclonal antibody (A02898-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MSI2 at approximately 35 kDa. The expected band size for MSI2 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02898-2-msi2-primary-antibodies-ihc-testing-1.jpgAnti-MSI2 Antibody Picoband®IHC analysis of MSI2 using anti-MSI2 antibody (A02898-2). MSI2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MSI2 Antibody (A02898-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02898-2-msi2-primary-antibodies-ihc-testing-2.jpgAnti-MSI2 Antibody Picoband®IHC analysis of MSI2 using anti-MSI2 antibody (A02898-2). MSI2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MSI2 Antibody (A02898-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02898-2-msi2-primary-antibodies-if-testing-1.jpgAnti-MSI2 Antibody Picoband®IF analysis of MSI2 using anti-MSI2 antibody (A02898-2). MSI2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MSI2 Antibody (A02898-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02898-2-msi2-primary-antibodies-if-testing-2.jpgAnti-MSI2 Antibody Picoband®IF analysis of MSI2 using anti-MSI2 antibody (A02898-2). MSI2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MSI2 Antibody (A02898-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02898-2-msi2-primary-antibodies-fcm-testing-1.jpgAnti-MSI2 Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-MSI2 antibody (A02898-2). Overlay histogram showing SH-SY5Y cells stained with A02898-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MSI2 Antibody (A02898-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243492026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06136-1-msrb2-primary-antibodies-wb-testing-1.jpgAnti-MSRB2 Antibody Picoband®Western blot analysis of MSRB2 using anti-MSRB2 antibody (A06136-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat heart tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse heart tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MSRB2 antigen affinity purified polyclonal antibody (A06136-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MSRB2 at approximately 15 kDa. The expected band size for MSRB2 is at 20 kDa. https://www.bosterbio.com/catalog/product/view/id/1243512026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243522026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07251-2-rpl24-primary-antibodies-wb-testing-1.jpgAnti-RPL24 Antibody Picoband® Western blot analysis of RPL24 using anti-RPL24 antibody (A07251-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPL24 antigen affinity purified polyclonal antibody (A07251-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPL24 at approximately 18 kDa. The expected band size for RPL24 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07251-2-rpl24-primary-antibodies-if-testing-2.jpgAnti-RPL24 Antibody Picoband® IF analysis of RPL24 using anti-RPL24 antibody (A07251-2). RPL24 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RPL24 Antibody (A07251-2) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1243532026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-inactivator-serping1-primary-antibodies-ihc-testing-1.jpgAnti-SERPING1/C1 Antibody Picoband® IHC analysis of Inactivator/SERPING1 using anti-Inactivator/SERPING1 antibody (A01221-3). Inactivator/SERPING1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Inactivator/SERPING1 Antibody (A01221-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-inactivator-serping1-primary-antibodies-ihc-testing-2.jpgAnti-SERPING1/C1 Antibody Picoband® IHC analysis of Inactivator/SERPING1 using anti-Inactivator/SERPING1 antibody (A01221-3). Inactivator/SERPING1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Inactivator/SERPING1 Antibody (A01221-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-inactivator-serping1-primary-antibodies-ihc-testing-3.jpgAnti-SERPING1/C1 Antibody Picoband® IHC analysis of Inactivator/SERPING1 using anti-Inactivator/SERPING1 antibody (A01221-3). Inactivator/SERPING1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Inactivator/SERPING1 Antibody (A01221-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-inactivator-serping1-primary-antibodies-ihc-testing-4.jpgAnti-SERPING1/C1 Antibody Picoband® IHC analysis of Inactivator/SERPING1 using anti-Inactivator/SERPING1 antibody (A01221-3). Inactivator/SERPING1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Inactivator/SERPING1 Antibody (A01221-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-inactivator-serping1-primary-antibodies-ihc-testing-5.jpgAnti-SERPING1/C1 Antibody Picoband® IHC analysis of Inactivator/SERPING1 using anti-Inactivator/SERPING1 antibody (A01221-3). Inactivator/SERPING1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Inactivator/SERPING1 Antibody (A01221-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-inactivator-serping1-primary-antibodies-ihc-testing-6.jpgAnti-SERPING1/C1 Antibody Picoband® IHC analysis of Inactivator/SERPING1 using anti-Inactivator/SERPING1 antibody (A01221-3). Inactivator/SERPING1 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Inactivator/SERPING1 Antibody (A01221-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-inactivator-serping1-primary-antibodies-ihc-testing-7.jpgAnti-SERPING1/C1 Antibody Picoband® IHC analysis of Inactivator/SERPING1 using anti-Inactivator/SERPING1 antibody (A01221-3). Inactivator/SERPING1 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Inactivator/SERPING1 Antibody (A01221-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-serping1-primary-antibodies-wb-testing-1.jpgAnti-SERPING1/C1 Antibody Picoband®Western blot analysis of SERPING1 using anti-SERPING1 antibody (A01221-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human HepG2 whole cell lysates Lane 3: rat liver tissue lysates, Lane 4: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SERPING1 antigen affinity purified polyclonal antibody (A01221-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SERPING1 at approximately 100 kDa. The expected band size for SERPING1 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01221-3-serping1-primary-antibodies-fcm-testing-1.jpgAnti-SERPING1/C1 Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-SERPING1 antibody (A01221-3). Overlay histogram showing SH-SY5Y cells stained with A01221-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SERPING1 Antibody (A01221-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243542026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243552026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243562026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243572026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243582026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243592026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10053-2-dnajb9-primary-antibodies-wb-testing-1.jpgAnti-DNAJB9 Antibody Picoband®Western blot analysis of DNAJB9 using anti-DNAJB9 antibody (A10053-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJB9 antigen affinity purified polyclonal antibody (A10053-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNAJB9 at approximately 28 kDa. The expected band size for DNAJB9 is at 26 kDa. https://www.bosterbio.com/catalog/product/view/id/1243602026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243612026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243632026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11739-2-trim69-primary-antibodies-wb-testing-1.jpgAnti-TRIM69 Antibody Picoband®Western blot analysis of TRIM69 using anti-TRIM69 antibody (A11739-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIM69 antigen affinity purified polyclonal antibody (A11739-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIM69 at approximately 70 kDa. The expected band size for TRIM69 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11739-2-trim69-primary-antibodies-if-testing-1.jpgAnti-TRIM69 Antibody Picoband®IF analysis of TRIM69 using anti-TRIM69 antibody (A11739-2). TRIM69 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TRIM69 Antibody (A11739-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1243642026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243662026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04338-1-ube4b-primary-antibodies-wb-testing-1.jpgAnti-UBE4B Antibody Picoband®Western blot analysis of UBE4B using anti-UBE4B antibody (A04338-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UBE4B antigen affinity purified polyclonal antibody (A04338-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UBE4B at approximately 146 kDa. The expected band size for UBE4B is at 146 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04338-1-ube4b-primary-antibodies-if-testing-1.jpgAnti-UBE4B Antibody Picoband®IF analysis of UBE4B using anti-UBE4B antibody (A04338-1). UBE4B was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-UBE4B Antibody (A04338-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04338-1-ube4b-primary-antibodies-fcm-testing-1.jpgAnti-UBE4B Antibody Picoband®Flow Cytometry analysis of HEL cells using anti-UBE4B antibody (A04338-1). Overlay histogram showing HEL cells stained with A04338-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-UBE4B Antibody (A04338-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243672026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243682026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05004-1-uchl3-primary-antibodies-wb-testing-1.jpgAnti-UCHL3 Antibody Picoband®Western blot analysis of UCHL3 using anti-UCHL3 antibody (A05004-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse spleen tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UCHL3 antigen affinity purified polyclonal antibody (A05004-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UCHL3 at approximately 26 kDa. The expected band size for UCHL3 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05004-1-uchl3-primary-antibodies-wb-testing-1_1.jpgAnti-UCHL3 Antibody Picoband®Western blot analysis of UCHL3 using anti-UCHL3 antibody (A05004-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human SW620 whole cell lysates, Lane 4: human U-87MG whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UCHL3 antigen affinity purified polyclonal antibody (A05004-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UCHL3 at approximately 26 kDa. The expected band size for UCHL3 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05004-1-uchl3-primary-antibodies-if-testing-1.jpgAnti-UCHL3 Antibody Picoband®IF analysis of UCHL3 using anti-UCHL3 antibody (A05004-1) and anti-Alpha Tubulin antibody (M03989-3). UCHL3 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-UCHL3 Antibody (A05004-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05004-1-uchl3-primary-antibodies-ip-testing-1.jpgAnti-UCHL3 Antibody Picoband®Immunoprecipitating UCHL3 in Hela whole cell lysate. Western blot analysis of UCHL3 using anti-UCHL3 antibody (A05004-1). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-UCHL3 antibody in Hela whole cell lysate, Lane 3: anti-UCHL3 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-UCHL3 antigen affinity purified polyclonal antibody (A05004-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for UCHL3 at approximately 26 kDa. The expected band size for UCHL3 is at 26 kDa. https://www.bosterbio.com/catalog/product/view/id/1243692026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243702026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243712026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15043-dctn6-primary-antibodies-wb-testing-1.jpgAnti-DCTN6 Antibody Picoband®Western blot analysis of DCTN6 using anti-DCTN6 antibody (A15043). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human COLO-320 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse lung tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DCTN6 antigen affinity purified polyclonal antibody (A15043) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DCTN6 at approximately 25 kDa. The expected band size for DCTN6 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15043-dctn6-primary-antibodies-ihc-testing-1.jpgAnti-DCTN6 Antibody Picoband®IHC analysis of DCTN6 using anti-DCTN6 antibody (A15043). DCTN6 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCTN6 Antibody (A15043) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15043-dctn6-primary-antibodies-ihc-testing-2.jpgAnti-DCTN6 Antibody Picoband®IHC analysis of DCTN6 using anti-DCTN6 antibody (A15043). DCTN6 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCTN6 Antibody (A15043) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15043-dctn6-primary-antibodies-ihc-testing-3.jpgAnti-DCTN6 Antibody Picoband®IHC analysis of DCTN6 using anti-DCTN6 antibody (A15043). DCTN6 was detected in a paraffin-embedded section of human lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DCTN6 Antibody (A15043) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15043-dctn6-primary-antibodies-ip-testing-1.jpgAnti-DCTN6 Antibody Picoband®Immunoprecipitating DCTN6 in A549 whole cell lysate. Western blot analysis of DCTN6 using anti-DCTN6 antibody (A15043). Lane 1: A549 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-DCTN6 antibody in A549 whole cell lysate, Lane 3: anti-DCTN6 antibody (2μg) + A549 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-DCTN6 antigen affinity purified polyclonal antibody (A15043) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for DCTN6 at approximately 25 kDa. The expected band size for DCTN6 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15043-dctn6-primary-antibodies-fcm-testing-1.jpgAnti-DCTN6 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-DCTN6 antibody (A15043). Overlay histogram showing 293T cells stained with A15043 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DCTN6 Antibody (A15043, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243722026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08440-1-ddx46-primary-antibodies-wb-testing-1.jpgAnti-DDX46 Antibody Picoband®Western blot analysis of DDX46 using anti-DDX46 antibody (A08440-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DDX46 antigen affinity purified polyclonal antibody (A08440-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DDX46 at approximately 150 kDa. The expected band size for DDX46 is at 117 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08440-1-ddx46-primary-antibodies-ihc-testing-1.jpgAnti-DDX46 Antibody Picoband®IHC analysis of DDX46 using anti-DDX46 antibody (A08440-1). DDX46 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX46 Antibody (A08440-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08440-1-ddx46-primary-antibodies-ihc-testing-2.jpgAnti-DDX46 Antibody Picoband®IHC analysis of DDX46 using anti-DDX46 antibody (A08440-1). DDX46 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX46 Antibody (A08440-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08440-1-ddx46-primary-antibodies-if-testing-1.jpgAnti-DDX46 Antibody Picoband®IF analysis of DDX46 using anti-DDX46 antibody (A08440-1) and anti-Alpha Tubulin antibody (M03989-3). DDX46 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DDX46 Antibody (A08440-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08440-1-ddx46-primary-antibodies-ip-testing-1.jpgAnti-DDX46 Antibody Picoband®Immunoprecipitating DDX46 in Hela whole cell lysate. Western blot analysis of DDX46 using anti-DDX46 antibody (A08440-1). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-DDX46 antibody in Hela whole cell lysate, Lane 3: anti-DDX46 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-DDX46 antigen affinity purified polyclonal antibody (A08440-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for DDX46 at approximately 150 kDa. The expected band size for DDX46 is at 117 kDa. https://www.bosterbio.com/catalog/product/view/id/1243732026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243742026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03205-2-desmocollin-2-dsc2-primary-antibodies-wb-testing-1.jpgAnti-DSC2 Antibody Picoband® Western blot analysis of Desmocollin 2/DSC2 using anti-Desmocollin 2/DSC2 antibody (A03205-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat heart tissue lysates, Lane 4: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Desmocollin 2/DSC2 antigen affinity purified polyclonal antibody (A03205-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Desmocollin 2/DSC2 at approximately 110 kDa. The expected band size for Desmocollin 2/DSC2 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03205-2-desmocollin-2-dsc2-primary-antibodies-ihc-testing-2.jpgAnti-DSC2 Antibody Picoband® IHC analysis of Desmocollin 2/DSC2 using anti-Desmocollin 2/DSC2 antibody (A03205-2). Desmocollin 2/DSC2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Desmocollin 2/DSC2 Antibody (A03205-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03205-2-desmocollin-2-dsc2-primary-antibodies-ihc-testing-3.jpgAnti-DSC2 Antibody Picoband® IHC analysis of Desmocollin 2/DSC2 using anti-Desmocollin 2/DSC2 antibody (A03205-2). Desmocollin 2/DSC2 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Desmocollin 2/DSC2 Antibody (A03205-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03205-2-desmocollin-2-dsc2-primary-antibodies-ihc-testing-4.jpgAnti-DSC2 Antibody Picoband® IHC analysis of Desmocollin 2/DSC2 using anti-Desmocollin 2/DSC2 antibody (A03205-2). Desmocollin 2/DSC2 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Desmocollin 2/DSC2 Antibody (A03205-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03205-2-desmocollin-2-dsc2-primary-antibodies-ihc-testing-5.jpgAnti-DSC2 Antibody Picoband® IHC analysis of Desmocollin 2/DSC2 using anti-Desmocollin 2/DSC2 antibody (A03205-2). Desmocollin 2/DSC2 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-Desmocollin 2/DSC2 Antibody (A03205-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03205-2-dsc2-primary-antibodies-wb-testing-1.jpgAnti-DSC2 Antibody Picoband®Western blot analysis of DSC2 using anti-DSC2 antibody (A03205-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat H9C2(2-1) whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DSC2 antigen affinity purified polyclonal antibody (A03205-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DSC2 at approximately 120 kDa. The expected band size for DSC2 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03205-2-dsc2-primary-antibodies-fcm-testing-1.jpgAnti-DSC2 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-DSC2 antibody (A03205-2). Overlay histogram showing 293T cells stained with A03205-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-DSC2 Antibody (A03205-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243752026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243762026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243772026-03-16T05:08:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04331-2-alox15b-primary-antibodies-wb-testing-1.jpgAnti-15 Lipoxygenase 2/ALOX15B AntibodyWestern blot analysis of ALOX15B using anti-ALOX15B antibody (A04331-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALOX15B antigen affinity purified polyclonal antibody (A04331-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALOX15B at approximately 76 kDa. The expected band size for ALOX15B is at 76 kDa. https://www.bosterbio.com/catalog/product/view/id/1243782026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243792026-03-16T05:08:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243802026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243812026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243822026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243832026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243842026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1243852026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12847-1-ube2f-primary-antibodies-wb-testing-1.jpgAnti-UBE2F Antibody Picoband®Western blot analysis of UBE2F using anti-UBE2F antibody (A12847-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat ovary tissue lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UBE2F antigen affinity purified polyclonal antibody (A12847-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UBE2F at approximately 21 kDa. The expected band size for UBE2F is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12847-1-ube2f-primary-antibodies-ihc-testing-1.jpgAnti-UBE2F Antibody Picoband®IHC analysis of UBE2F using anti-UBE2F antibody (A12847-1). UBE2F was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UBE2F Antibody (A12847-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12847-1-ube2f-primary-antibodies-if-testing-1.jpgAnti-UBE2F Antibody Picoband®IF analysis of UBE2F using anti-UBE2F antibody (A12847-1) and anti-Alpha Tubulin antibody (M03989-3). UBE2F was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-UBE2F Antibody (A12847-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12847-1-ube2f-primary-antibodies-fcm-testing-1.jpgAnti-UBE2F Antibody Picoband®Flow Cytometry analysis of K562 cells using anti-UBE2F antibody (A12847-1). Overlay histogram showing K562 cells stained with A12847-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-UBE2F Antibody (A12847-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1243862026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek0791.pngHuman IL-17D ELISA Kit PicoKine®Human IL-17D PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1243872026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2261.jpgHuman PIGR ELISA Kit PicoKine®Human PIGR PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1243882026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2255.pngHuman PILRA ELISA Kit PicoKine®Human PRLRA PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1243892026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2256.jpgHuman PILRB ELISA Kit PicoKine®Human PRLRB PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1243902026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2257.jpgHuman PKLR ELISA Kit PicoKine®Human PKLR PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1243912026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2258.jpgHuman PNP ELISA Kit PicoKine®Human PNP PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1243922026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2259.pngHuman PREP ELISA Kit PicoKine®Human PREP PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1243932026-03-10T04:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2260.pngHuman Protogenin ELISA Kit PicoKine®Human Protogenin PicoKine ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-plasmodium-falciparum-syntaxin-qa-snare-family-antibody-dz41446-boster.html2026-03-10T04:36:12+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-blind-cave-fish-cd37-antibody-dz41448-boster.html2026-03-10T04:36:12+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-rpl18-picoband-trade-antibody-a07057-3-boster.html2026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-wb-testing-1.jpgAnti-RPL18 Antibody Picoband® Western blot analysis of RPL18 using anti-RPL18 antibody (A07057-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Daudi whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPL18 antigen affinity purified polyclonal antibody (Catalog # A07057-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPL18 at approximately 23 kDa. The expected band size for RPL18 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-ihc-testing-2.jpgAnti-RPL18 Antibody Picoband® IHC analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-ihc-testing-3.jpgAnti-RPL18 Antibody Picoband® IHC analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-ihc-testing-4.jpgAnti-RPL18 Antibody Picoband® IHC analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-ihc-testing-5.jpgAnti-RPL18 Antibody Picoband® IHC analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-ihc-testing-6.jpgAnti-RPL18 Antibody Picoband® IHC analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-ihc-testing-7.jpgAnti-RPL18 Antibody Picoband® IHC analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-ihc-testing-8.jpgAnti-RPL18 Antibody Picoband® IHC analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-if-testing-9.jpgAnti-RPL18 Antibody Picoband® IF analysis of RPL18 using anti-RPL18 antibody (A07057-3). RPL18 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RPL18 Antibody (A07057-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07057-3-rpl18-primary-antibodies-fcm-testing-10.pngAnti-RPL18 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-RPL18 antibody (A07057-3). Overlay histogram showing Hela cells stained with A07057-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPL18 Antibody (A07057-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pxylp1-picoband-trade-antibody-a13883-1-boster.html2026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13883-1-pxylp1-primary-antibodies-wb-testing-1.jpgAnti-PXYLP1 Antibody Picoband® Western blot analysis of ACPL2/PXYLP1 using anti-ACPL2/PXYLP1 antibody (A13883-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACPL2/PXYLP1 antigen affinity purified polyclonal antibody (Catalog # A13883-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACPL2/PXYLP1 at approximately 70 kDa. The expected band size for ACPL2/PXYLP1 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13883-1-pxylp1-primary-antibodies-fcm-testing-2.pngAnti-PXYLP1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-ACPL2/PXYLP1 antibody (A13883-1). Overlay histogram showing SH-SY5Y cells stained with A13883-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ACPL2/PXYLP1 Antibody (A13883-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-magel2-picoband-trade-antibody-a06305-1-boster.html2026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06305-1-magel2-primary-antibodies-wb-testing-1.jpgAnti-MAGEL2 Antibody Picoband® Western blot analysis of MAGEL2 using anti-MAGEL2 antibody (A06305-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAGEL2 antigen affinity purified polyclonal antibody (Catalog # A06305-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAGEL2 at approximately 133 kDa. The expected band size for MAGEL2 is at 133 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06305-1-magel2-primary-antibodies-ihc-testing-2.jpgAnti-MAGEL2 Antibody Picoband® IHC analysis of MAGEL2 using anti-MAGEL2 antibody (A06305-1). MAGEL2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAGEL2 Antibody (A06305-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06305-1-magel2-primary-antibodies-ihc-testing-3.jpgAnti-MAGEL2 Antibody Picoband® IHC analysis of MAGEL2 using anti-MAGEL2 antibody (A06305-1). MAGEL2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAGEL2 Antibody (A06305-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06305-1-magel2-primary-antibodies-fcm-testing-4.pngAnti-MAGEL2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MAGEL2 antibody (A06305-1). Overlay histogram showing JK cells stained with A06305-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAGEL2 Antibody (A06305-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-map4k5-picoband-trade-antibody-a10186-2-boster.html2026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10186-2-map4k5-primary-antibodies-wb-testing-1.jpgAnti-MAP4K5 Antibody Picoband® Western blot analysis of MAP4K5 using anti-MAP4K5 antibody (A10186-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP4K5 antigen affinity purified polyclonal antibody (Catalog # A10186-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP4K5 at approximately 95 kDa. The expected band size for MAP4K5 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10186-2-map4k5-primary-antibodies-fcm-testing-2.pngAnti-MAP4K5 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MAP4K5 antibody (A10186-2). Overlay histogram showing HepG2 cells stained with A10186-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAP4K5 Antibody (A10186-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-myogenin-myog-picoband-trade-antibody-a03238-1-boster.html2026-03-17T05:15:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03238-1-myog-primary-antibodies-wb-testing-1.jpgAnti-Myogenin/MYOG Antibody Picoband® Western blot analysis of Myogenin/MYOG using anti-Myogenin/MYOG antibody (A03238-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: monkey skeletal muscle tissue lysates, Lane 2: rat skeletal muscle tissue lysates, Lane 3: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Myogenin/MYOG antigen affinity purified polyclonal antibody (Catalog # A03238-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Myogenin/MYOG at approximately 40 kDa. The expected band size for Myogenin/MYOG is at 25 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-lctl-picoband-trade-antibody-a14882-2-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14882-2-lctl-primary-antibodies-wb-testing-1.jpgAnti-LCTL Antibody Picoband® Western blot analysis of LCTL using anti-LCTL antibody (A14882-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LCTL antigen affinity purified polyclonal antibody (Catalog # A14882-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LCTL at approximately 70 kDa. The expected band size for LCTL is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14882-2-lctl-primary-antibodies-fcm-testing-2.pngAnti-LCTL Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-LCTL antibody (A14882-2). Overlay histogram showing HepG2 cells stained with A14882-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LCTL Antibody (A14882-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mvd-picoband-trade-antibody-a01631-2-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01631-2-mvd-primary-antibodies-wb-testing-1.jpgAnti-MVD Antibody Picoband® Western blot analysis of MVD using anti-MVD antibody (A01631-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MVD antigen affinity purified polyclonal antibody (Catalog # A01631-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MVD at approximately 43 kDa. The expected band size for MVD is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01631-2-mvd-primary-antibodies-ihc-testing-3.jpgAnti-MVD Antibody Picoband®IHC analysis of MVD using anti-MVD antibody (A01631-2). MVD was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MVD Antibody (A01631-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01631-2-mvd-primary-antibodies-ihc-testing-2.jpgAnti-MVD Antibody Picoband® IHC analysis of MVD using anti-MVD antibody (A01631-2). MVD was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MVD Antibody (A01631-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01631-2-mvd-primary-antibodies-fcm-testing-3.pngAnti-MVD Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MVD antibody (A01631-2). Overlay histogram showing MCF-7 cells stained with A01631-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MVD Antibody (A01631-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mzb1-picoband-trade-antibody-a08281-1-boster.html2026-03-16T09:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08281-1-mzb1-primary-antibodies-wb-testing-1.jpgAnti-MZB1 Antibody Picoband® Western blot analysis of MZB1 using anti-MZB1 antibody (A08281-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MZB1 antigen affinity purified polyclonal antibody (Catalog # A08281-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MZB1 at approximately 19 kDa. The expected band size for MZB1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08281-1-mzb1-primary-antibodies-ihc-testing-2.jpgAnti-MZB1 Antibody Picoband® IHC analysis of MZB1 using anti-MZB1 antibody (A08281-1). MZB1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MZB1 Antibody (A08281-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08281-1-mzb1-primary-antibodies-ihc-testing-3.jpgAnti-MZB1 Antibody Picoband® IHC analysis of MZB1 using anti-MZB1 antibody (A08281-1). MZB1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MZB1 Antibody (A08281-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08281-1-mzb1-primary-antibodies-ihc-testing-4.jpgAnti-MZB1 Antibody Picoband® IHC analysis of MZB1 using anti-MZB1 antibody (A08281-1). MZB1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MZB1 Antibody (A08281-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08281-1-mzb1-primary-antibodies-if-testing-5.jpgAnti-MZB1 Antibody Picoband® IF analysis of MZB1 using anti-MZB1 antibody (A08281-1). MZB1 was detected in an immunocytochemical section of Jurkat cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MZB1 Antibody (A08281-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08281-1-mzb1-primary-antibodies-fcm-testing-6.pngAnti-MZB1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MZB1 antibody (A08281-1). Overlay histogram showing JK cells stained with A08281-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MZB1 Antibody (A08281-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-l3mbtl2-picoband-trade-antibody-a08416-1-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08416-1-l3mbtl2-primary-antibodies-wb-testing-1.jpgAnti-L3MBTL2 Antibody Picoband® Western blot analysis of L3MBTL2 using anti-L3MBTL2 antibody (A08416-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MOLT-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-L3MBTL2 antigen affinity purified polyclonal antibody (Catalog # A08416-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for L3MBTL2 at approximately 79 kDa. The expected band size for L3MBTL2 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08416-1-l3mbtl2-primary-antibodies-ihc-testing-2.jpgAnti-L3MBTL2 Antibody Picoband® IHC analysis of L3MBTL2 using anti-L3MBTL2 antibody (A08416-1). L3MBTL2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-L3MBTL2 Antibody (A08416-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08416-1-l3mbtl2-primary-antibodies-ihc-testing-3.jpgAnti-L3MBTL2 Antibody Picoband® IHC analysis of L3MBTL2 using anti-L3MBTL2 antibody (A08416-1). L3MBTL2 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-L3MBTL2 Antibody (A08416-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08416-1-l3mbtl2-primary-antibodies-ihc-testing-4.jpgAnti-L3MBTL2 Antibody Picoband® IHC analysis of L3MBTL2 using anti-L3MBTL2 antibody (A08416-1). L3MBTL2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-L3MBTL2 Antibody (A08416-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08416-1-l3mbtl2-primary-antibodies-if-testing-5.jpgAnti-L3MBTL2 Antibody Picoband® IF analysis of L3MBTL2 using anti-L3MBTL2 antibody (A08416-1) and anti-Beta Tubulin antibody (M01857-3). L3MBTL2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-L3MBTL2 Antibody (A08416-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-lad1-picoband-trade-antibody-a07940-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07940-lad1-primary-antibodies-wb-testing-1.jpgAnti-LAD1 Antibody Picoband® Western blot analysis of LAD1 using anti-LAD1 antibody (A07940). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LAD1 antigen affinity purified polyclonal antibody (Catalog # A07940) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LAD1 at approximately 65 kDa. The expected band size for LAD1 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07940-lad1-primary-antibodies-if-testing-2.jpgAnti-LAD1 Antibody Picoband® IF analysis of LAD1 using anti-LAD1 antibody (A07940). LAD1 was detected in an immunocytochemical section of Caco-2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LAD1 Antibody (A07940) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07940-lad1-primary-antibodies-fcm-testing-3.pngAnti-LAD1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-LAD1 antibody (A07940). Overlay histogram showing HepG2 cells stained with A07940 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LAD1 Antibody (A07940, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lage3-picoband-trade-antibody-a15245-1-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15245-1-lage3-primary-antibodies-wb-testing-1.jpgAnti-LAGE3 Antibody Picoband® Western blot analysis of LAGE3 using anti-LAGE3 antibody (A15245-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LAGE3 antigen affinity purified polyclonal antibody (Catalog # A15245-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LAGE3 at approximately 17 kDa. The expected band size for LAGE3 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15245-1-lage3-primary-antibodies-if-testing-2.jpgAnti-LAGE3 Antibody Picoband® IF analysis of LAGE3 using anti-LAGE3 antibody (A15245-1) and anti-Beta Tubulin antibody (M01857-3). LAGE3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LAGE3 Antibody (A15245-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-lair1-picoband-trade-antibody-a03470-2-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03470-2-lair1-primary-antibodies-wb-testing-1.jpgAnti-LAIR1 Antibody Picoband® Western blot analysis of LAIR1 using anti-LAIR1 antibody (A03470-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LAIR1 antigen affinity purified polyclonal antibody (Catalog # A03470-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LAIR1 at approximately 40 kDa. The expected band size for LAIR1 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03470-2-lair1-primary-antibodies-fcm-testing-2.pngAnti-LAIR1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-LAIR1 antibody (A03470-2). Overlay histogram showing K562 cells stained with A03470-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LAIR1 Antibody (A03470-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ldah-picoband-trade-antibody-a13985-boster.html2026-03-28T05:00:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13985-ldah-primary-antibodies-wb-testing-1.jpgAnti-LDAH Antibody Picoband® Western blot analysis of C2orf43/LDAH using anti-C2orf43/LDAH antibody (A13985). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: monkey COS-7 whole cell lysates, Lane 6: human SK-N-SH whole cell lysates, Lane 7: human SH-SY5Y whole cell lysates, Lane 8: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C2orf43/LDAH antigen affinity purified polyclonal antibody (Catalog # A13985) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C2orf43/LDAH at approximately 37 kDa. The expected band size for C2orf43/LDAH is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13985-ldah-primary-antibodies-wb-testing-2.jpgAnti-LDAH Antibody Picoband® Western blot analysis of C2orf43/LDAH using anti-C2orf43/LDAH antibody (A13985). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat liver tissue lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat RH-35 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C2orf43/LDAH antigen affinity purified polyclonal antibody (Catalog # A13985) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C2orf43/LDAH at approximately 37 kDa. The expected band size for C2orf43/LDAH is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13985-ldah-primary-antibodies-ihc-testing-3.jpgAnti-LDAH Antibody Picoband® IHC analysis of C2orf43/LDAH using anti-C2orf43/LDAH antibody (A13985). C2orf43/LDAH was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C2orf43/LDAH Antibody (A13985) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13985-ldah-primary-antibodies-ihc-testing-4.jpgAnti-LDAH Antibody Picoband® IHC analysis of C2orf43/LDAH using anti-C2orf43/LDAH antibody (A13985). C2orf43/LDAH was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C2orf43/LDAH Antibody (A13985) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13985-ldah-primary-antibodies-ihc-testing-5.jpgAnti-LDAH Antibody Picoband® IHC analysis of C2orf43/LDAH using anti-C2orf43/LDAH antibody (A13985). C2orf43/LDAH was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C2orf43/LDAH Antibody (A13985) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13985-ldah-primary-antibodies-ihc-testing-6.jpgAnti-LDAH Antibody Picoband® IHC analysis of C2orf43/LDAH using anti-C2orf43/LDAH antibody (A13985). C2orf43/LDAH was detected in a paraffin-embedded section of rat alcoholic liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C2orf43/LDAH Antibody (A13985) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13985-ldah-primary-antibodies-fcm-testing-7.pngAnti-LDAH Antibody Picoband® Flow Cytometry analysis of JK cells using anti-C2orf43/LDAH antibody (A13985). Overlay histogram showing JK cells stained with A13985 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-C2orf43/LDAH Antibody (A13985, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ldoc1-picoband-trade-antibody-a09804-2-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09804-2-ldoc1-primary-antibodies-wb-testing-1.jpgAnti-LDOC1 Antibody Picoband® Western blot analysis of LDOC1 using anti-LDOC1 antibody (A09804-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LDOC1 antigen affinity purified polyclonal antibody (Catalog # A09804-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LDOC1 at approximately 15 kDa. The expected band size for LDOC1 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09804-2-ldoc1-primary-antibodies-if-testing-2.jpgAnti-LDOC1 Antibody Picoband® IF analysis of LDOC1 using anti-LDOC1 antibody (A09804-2) and anti-Beta Tubulin antibody (M01857-3). LDOC1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LDOC1 Antibody (A09804-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09804-2-ldoc1-primary-antibodies-fcm-testing-3.pngAnti-LDOC1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-LDOC1 antibody (A09804-2). Overlay histogram showing U251 cells stained with A09804-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LDOC1 Antibody (A09804-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lekr1-picoband-trade-antibody-a15972-1-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15972-1-lekr1-primary-antibodies-wb-testing-1.jpgAnti-LEKR1 Antibody Picoband® Western blot analysis of LEKR1 using anti-LEKR1 antibody (A15972-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human SiHa whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LEKR1 antigen affinity purified polyclonal antibody (Catalog # A15972-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LEKR1 at approximately 16 kDa. The expected band size for LEKR1 is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15972-1-lekr1-primary-antibodies-ihc-testing-2.jpgAnti-LEKR1 Antibody Picoband® IHC analysis of LEKR1 using anti-LEKR1 antibody (A15972-1). LEKR1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEKR1 Antibody (A15972-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15972-1-lekr1-primary-antibodies-if-testing-3.jpgAnti-LEKR1 Antibody Picoband® IF analysis of LEKR1 using anti-LEKR1 antibody (A15972-1). LEKR1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LEKR1 Antibody (A15972-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-lemd3-picoband-trade-antibody-a04957-1-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04957-1-lemd3-primary-antibodies-wb-testing-1.jpgAnti-LEMD3 Antibody Picoband® Western blot analysis of MAN1/LEMD3 using anti-MAN1/LEMD3 antibody (A04957-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAN1/LEMD3 antigen affinity purified polyclonal antibody (Catalog # A04957-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAN1/LEMD3 at approximately 120 kDa. The expected band size for MAN1/LEMD3 is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04957-1-lemd3-primary-antibodies-fcm-testing-2.pngAnti-LEMD3 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MAN1/LEMD3 antibody (A04957-1). Overlay histogram showing 293T cells stained with A04957-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAN1/LEMD3 Antibody (A04957-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-leo1-picoband-trade-antibody-a06433-2-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-wb-testing-1.jpgAnti-LEO1 Antibody Picoband® Western blot analysis of LEO1 using anti-LEO1 antibody (A06433-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: human RT4 whole cell lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LEO1 antigen affinity purified polyclonal antibody (Catalog # A06433-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LEO1 at approximately 105 kDa. The expected band size for LEO1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-2.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-3.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of human cervica squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-4.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-5.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-6.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-7.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-8.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-ihc-testing-9.jpgAnti-LEO1 Antibody Picoband® IHC analysis of LEO1 using anti-LEO1 antibody (A06433-2). LEO1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LEO1 Antibody (A06433-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-if-testing-10.jpgAnti-LEO1 Antibody Picoband® IF analysis of LEO1 using anti-LEO1 antibody (A06433-2) and anti-Beta Tubulin antibody (M01857-3). LEO1 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LEO1 Antibody (A06433-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06433-2-leo1-primary-antibodies-fcm-testing-11.pngAnti-LEO1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-LEO1 antibody (A06433-2). Overlay histogram showing JK cells stained with A06433-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LEO1 Antibody (A06433-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lgi4-picoband-trade-antibody-a12305-1-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-wb-testing-1.jpgAnti-LGI4 Antibody Picoband® Western blot analysis of LGI4 using anti-LGI4 antibody (A12305-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat stomach tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LGI4 antigen affinity purified polyclonal antibody (Catalog # A12305-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LGI4 at approximately 59 kDa. The expected band size for LGI4 is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-ihc-testing-2.jpgAnti-LGI4 Antibody Picoband® IHC analysis of LGI4 using anti-LGI4 antibody (A12305-1). LGI4 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGI4 Antibody (A12305-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-ihc-testing-3.jpgAnti-LGI4 Antibody Picoband® IHC analysis of LGI4 using anti-LGI4 antibody (A12305-1). LGI4 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGI4 Antibody (A12305-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-ihc-testing-4.jpgAnti-LGI4 Antibody Picoband® IHC analysis of LGI4 using anti-LGI4 antibody (A12305-1). LGI4 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGI4 Antibody (A12305-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-ihc-testing-5.jpgAnti-LGI4 Antibody Picoband® IHC analysis of LGI4 using anti-LGI4 antibody (A12305-1). LGI4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGI4 Antibody (A12305-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-ihc-testing-6.jpgAnti-LGI4 Antibody Picoband® IHC analysis of LGI4 using anti-LGI4 antibody (A12305-1). LGI4 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGI4 Antibody (A12305-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-if-testing-7.jpgAnti-LGI4 Antibody Picoband® IF analysis of LGI4 using anti-LGI4 antibody (A12305-1). LGI4 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LGI4 Antibody (A12305-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12305-1-lgi4-primary-antibodies-fcm-testing-8.pngAnti-LGI4 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-LGI4 antibody (A12305-1). Overlay histogram showing JK cells stained with A12305-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LGI4 Antibody (A12305-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lin7c-picoband-trade-antibody-a07929-1-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07929-1-lin7c-primary-antibodies-wb-testing-1.jpgAnti-LIN7C Antibody Picoband® Western blot analysis of LIN7C using anti-LIN7C antibody (A07929-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: rat brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIN7C antigen affinity purified polyclonal antibody (Catalog # A07929-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIN7C at approximately 22 kDa. The expected band size for LIN7C is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07929-1-lin7c-primary-antibodies-ihc-testing-2.jpgAnti-LIN7C Antibody Picoband® IHC analysis of LIN7C using anti-LIN7C antibody (A07929-1). LIN7C was detected in a paraffin-embedded section of human adrenal adenomas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LIN7C Antibody (A07929-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07929-1-lin7c-primary-antibodies-ihc-testing-3.jpgAnti-LIN7C Antibody Picoband® IHC analysis of LIN7C using anti-LIN7C antibody (A07929-1). LIN7C was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LIN7C Antibody (A07929-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07929-1-lin7c-primary-antibodies-ihc-testing-4.jpgAnti-LIN7C Antibody Picoband® IHC analysis of LIN7C using anti-LIN7C antibody (A07929-1). LIN7C was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LIN7C Antibody (A07929-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07929-1-lin7c-primary-antibodies-ihc-testing-5.jpgAnti-LIN7C Antibody Picoband® IHC analysis of LIN7C using anti-LIN7C antibody (A07929-1). LIN7C was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LIN7C Antibody (A07929-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07929-1-lin7c-primary-antibodies-fcm-testing-6.pngAnti-LIN7C Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-LIN7C antibody (A07929-1). Overlay histogram showing THP-1 cells stained with A07929-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LIN7C Antibody (A07929-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07929-1-lin7c-primary-antibodies-fcm-testing-7.pngAnti-LIN7C Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-LIN7C antibody (A07929-1). Overlay histogram showing THP-1 cells stained with A07929-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LIN7C Antibody (A07929-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-lin9-picoband-trade-antibody-a06333-1-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06333-1-lin9-primary-antibodies-wb-testing-1.jpgAnti-LIN9 Antibody Picoband® Western blot analysis of LIN9 using anti-LIN9 antibody (A06333-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIN9 antigen affinity purified polyclonal antibody (Catalog # A06333-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIN9 at approximately 65 kDa. The expected band size for LIN9 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06333-1-lin9-primary-antibodies-wb-testing-2.jpgAnti-LIN9 Antibody Picoband® Western blot analysis of LIN9 using anti-LIN9 antibody (A06333-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysatess, Lane 2: human U2OS whole cell lysatess, Lane 3: human T98G whole cell lysatess. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 70 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIN9 antigen affinity purified polyclonal antibody (Catalog # A06333-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LIN9 at approximately 65 kDa. The expected band size for LIN9 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06333-1-lin9-primary-antibodies-if-testing-3.jpgAnti-LIN9 Antibody Picoband® IF analysis of LIN9 using anti-LIN9 antibody (A06333-1) and anti-Beta Tubulin antibody (M01857-3). LIN9 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LIN9 Antibody (A06333-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-lmo7-picoband-trade-antibody-a05712-2-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05712-2-lmo7-primary-antibodies-wb-testing-1.jpgAnti-LMO7 Antibody Picoband® Western blot analysis of LMO7 using anti-LMO7 antibody (A05712-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMO7 antigen affinity purified polyclonal antibody (Catalog # A05712-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LMO7 at approximately 150 kDa. The expected band size for LMO7 is at 193 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05712-2-lmo7-primary-antibodies-fcm-testing-2.pngAnti-LMO7 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-LMO7 antibody (A05712-2). Overlay histogram showing Caco-2 cells stained with A05712-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LMO7 Antibody (A05712-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lonrf1-picoband-trade-antibody-a14796-boster.html2026-03-17T05:15:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14796-lonrf1-primary-antibodies-wb-testing-1.jpgAnti-LONRF1 Antibody Picoband® Western blot analysis of LONRF1 using anti-LONRF1 antibody (A14796). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LONRF1 antigen affinity purified polyclonal antibody (Catalog # A14796) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LONRF1 at approximately 100 kDa. The expected band size for LONRF1 is at 87 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-lonrf2-picoband-trade-antibody-a16358-1-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16358-1-lonrf2-primary-antibodies-wb-testing-1.jpgAnti-LONRF2 Antibody Picoband® Western blot analysis of LONRF2 using anti-LONRF2 antibody (A16358-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human A562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LONRF2 antigen affinity purified polyclonal antibody (Catalog # A16358-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LONRF2 at approximately 95 kDa. The expected band size for LONRF2 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16358-1-lonrf2-primary-antibodies-fcm-testing-2.pngAnti-LONRF2 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-LONRF2 antibody (A16358-1). Overlay histogram showing 293T cells stained with A16358-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LONRF2 Antibody (A16358-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lpar3-picoband-trade-antibody-a06597-3-boster.html2026-04-05T05:00:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06597-3-lpar3-primary-antibodies-wb-testing-1.jpgAnti-LPAR3 Antibody Picoband® Western blot analysis of EDG7/LPAR3 using anti-EDG7/LPAR3 antibody (A06597-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates, Lane 3: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EDG7/LPAR3 antigen affinity purified polyclonal antibody (Catalog # A06597-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EDG7/LPAR3 at approximately 43 kDa. The expected band size for EDG7/LPAR3 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06597-3-lpar3-primary-antibodies-fcm-testing-2.pngAnti-LPAR3 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-EDG7/LPAR3 antibody (A06597-3). Overlay histogram showing RT4 cells stained with A06597-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-EDG7/LPAR3 Antibody (A06597-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lpcat2-picoband-trade-antibody-a07471-2-boster.html2026-03-16T09:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07471-2-lpcat2-primary-antibodies-wb-testing-1.jpgAnti-LPCAT2 Antibody Picoband® Western blot analysis of LPCAT2 using anti-LPCAT2 antibody (A07471-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat thymus tissue lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LPCAT2 antigen affinity purified polyclonal antibody (Catalog # A07471-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LPCAT2 at approximately 53 kDa. The expected band size for LPCAT2 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07471-2-lpcat2-primary-antibodies-ihc-testing-2.jpgAnti-LPCAT2 Antibody Picoband® IHC analysis of LPCAT2 using anti-LPCAT2 antibody (A07471-2). LPCAT2 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LPCAT2 Antibody (A07471-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07471-2-lpcat2-primary-antibodies-ihc-testing-3.jpgAnti-LPCAT2 Antibody Picoband® IHC analysis of LPCAT2 using anti-LPCAT2 antibody (A07471-2). LPCAT2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LPCAT2 Antibody (A07471-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07471-2-lpcat2-primary-antibodies-fcm-testing-4.pngAnti-LPCAT2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-LPCAT2 antibody (A07471-2). Overlay histogram showing JK cells stained with A07471-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LPCAT2 Antibody (A07471-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lpgat1-picoband-trade-antibody-a13705-1-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13705-1-lpgat1-primary-antibodies-wb-testing-1.jpgAnti-LPGAT1 Antibody Picoband® Western blot analysis of LPGAT1 using anti-LPGAT1 antibody (A13705-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LPGAT1 antigen affinity purified polyclonal antibody (Catalog # A13705-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LPGAT1 at approximately 43 kDa. The expected band size for LPGAT1 is at 43 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-lrig2-picoband-trade-antibody-a09895-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09895-lrig2-primary-antibodies-wb-testing-1.jpgAnti-LRIG2 Antibody Picoband® Western blot analysis of LRIG2 using anti-LRIG2 antibody (A09895). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRIG2 antigen affinity purified polyclonal antibody (Catalog # A09895) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRIG2 at approximately 119 kDa. The expected band size for LRIG2 is at 119 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09895-lrig2-primary-antibodies-if-testing-2.jpgAnti-LRIG2 Antibody Picoband® IF analysis of LRIG2 using anti-LRIG2 antibody (A09895). LRIG2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LRIG2 Antibody (A09895) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09895-lrig2-primary-antibodies-fcm-testing-3.pngAnti-LRIG2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-LRIG2 antibody (A09895). Overlay histogram showing K562 cells stained with A09895 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRIG2 Antibody (A09895, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slc38a9-picoband-trade-antibody-a05824-2-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05824-2-slc38a9-primary-antibodies-wb-testing-1.jpgAnti-SLC38A9 Antibody Picoband® Western blot analysis of SLC38A9 using anti-SLC38A9 antibody (A05824-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC38A9 antigen affinity purified polyclonal antibody (Catalog # A05824-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC38A9 at approximately 64 kDa. The expected band size for SLC38A9 is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05824-2-slc38a9-primary-antibodies-if-testing-2.jpgAnti-SLC38A9 Antibody Picoband® IF analysis of SLC38A9 using anti-SLC38A9 antibody (A05824-2). SLC38A9 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SLC38A9 Antibody (A05824-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05824-2-slc38a9-primary-antibodies-fcm-testing-3.pngAnti-SLC38A9 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SLC38A9 antibody (A05824-2). Overlay histogram showing JK cells stained with A05824-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC38A9 Antibody (A05824-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-agl-picoband-trade-antibody-a02555-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02555-agl-primary-antibodies-wb-testing-1_1.jpgAnti-AGL Antibody Picoband® Western blot analysis of AGL using anti-AGL antibody (A02555). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AGL antigen affinity purified polyclonal antibody (Catalog # A02555) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AGL at approximately 175 kDa. The expected band size for AGL is at 175 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02555-agl-primary-antibodies-ihc-testing-2_1.jpgAnti-AGL Antibody Picoband® IHC analysis of AGL using anti-AGL antibody (A02555). AGL was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AGL Antibody (A02555) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02555-agl-primary-antibodies-if-testing-3.jpgAnti-AGL Antibody Picoband® IF analysis of AGL using anti-AGL antibody (A02555) and anti-Beta Tubulin antibody (M01857-3). AGL was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-AGL Antibody (A02555) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02555-agl-primary-antibodies-if-testing-4.jpgAnti-AGL Antibody Picoband® IF analysis of ABI1 using anti-ABI1 antibody (A02555). ABI1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ABI1 Antibody (A02555) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02555-agl-primary-antibodies-fcm-testing-5.jpgAnti-AGL Antibody Picoband® Flow Cytometry analysis of JK cells using anti-AGL antibody (A02555). Overlay histogram showing JK cells stained with A02555 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-AGL Antibody (A02555, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-aplp2-picoband-trade-antibody-a01232-1-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-wb-testing-1.jpgAnti-APLP2 Antibody Picoband® Western blot analysis of APLP2 using anti-APLP2 antibody (A01232-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APLP2 antigen affinity purified polyclonal antibody (Catalog # A01232-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for APLP2 at approximately 100-110 kDa. The expected band size for APLP2 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-ihc-testing-2.jpgAnti-APLP2 Antibody Picoband® IHC analysis of APLP2 using anti-APLP2 antibody (A01232-1). APLP2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APLP2 Antibody (A01232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-ihc-testing-3.jpgAnti-APLP2 Antibody Picoband® IHC analysis of APLP2 using anti-APLP2 antibody (A01232-1). APLP2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APLP2 Antibody (A01232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-ihc-testing-4.jpgAnti-APLP2 Antibody Picoband® IHC analysis of APLP2 using anti-APLP2 antibody (A01232-1). APLP2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APLP2 Antibody (A01232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-ihc-testing-5.jpgAnti-APLP2 Antibody Picoband® IHC analysis of APLP2 using anti-APLP2 antibody (A01232-1). APLP2 was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APLP2 Antibody (A01232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-ihc-testing-6.jpgAnti-APLP2 Antibody Picoband® IHC analysis of APLP2 using anti-APLP2 antibody (A01232-1). APLP2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APLP2 Antibody (A01232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-ihc-testing-7.jpgAnti-APLP2 Antibody Picoband® IHC analysis of APLP2 using anti-APLP2 antibody (A01232-1). APLP2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APLP2 Antibody (A01232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-if-testing-8.jpgAnti-APLP2 Antibody Picoband® IF analysis of APLP2 using anti-APLP2 antibody (A01232-1). APLP2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-APLP2 Antibody (A01232-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01232-1-aplp2-primary-antibodies-fcm-testing-9.pngAnti-APLP2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-APLP2 antibody (A01232-1). Overlay histogram showing HepG2 cells stained with A01232-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-APLP2 Antibody (A01232-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-psip1-picoband-trade-antibody-a01960-2-boster.html2026-03-16T09:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-wb-testing-1.jpgAnti-PSIP1 Antibody Picoband® Western blot analysis of PSIP1 using anti-PSIP1 antibody (A01960-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSIP1 antigen affinity purified polyclonal antibody (Catalog # A01960-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSIP1 at approximately 85 kDa. The expected band size for PSIP1 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-ihc-testing-2.jpgAnti-PSIP1 Antibody Picoband® IHC analysis of PSIP1 using anti-PSIP1 antibody (A01960-2). PSIP1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSIP1 Antibody (A01960-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-ihc-testing-3.jpgAnti-PSIP1 Antibody Picoband® IHC analysis of PSIP1 using anti-PSIP1 antibody (A01960-2). PSIP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSIP1 Antibody (A01960-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-ihc-testing-4.jpgAnti-PSIP1 Antibody Picoband® IHC analysis of PSIP1 using anti-PSIP1 antibody (A01960-2). PSIP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSIP1 Antibody (A01960-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-ihc-testing-5.jpgAnti-PSIP1 Antibody Picoband® IHC analysis of PSIP1 using anti-PSIP1 antibody (A01960-2). PSIP1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSIP1 Antibody (A01960-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-ihc-testing-6.jpgAnti-PSIP1 Antibody Picoband® IHC analysis of PSIP1 using anti-PSIP1 antibody (A01960-2). PSIP1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSIP1 Antibody (A01960-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-ihc-testing-7.jpgAnti-PSIP1 Antibody Picoband® IHC analysis of PSIP1 using anti-PSIP1 antibody (A01960-2). PSIP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSIP1 Antibody (A01960-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-if-testing-8.jpgAnti-PSIP1 Antibody Picoband® IF analysis of PSIP1 using anti-PSIP1 antibody (A01960-2) and anti-Beta Tubulin antibody (M01857-3). PSIP1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PSIP1 Antibody (A01960-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01960-2-psip1-primary-antibodies-fcm-testing-9.pngAnti-PSIP1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-PSIP1 antibody (A01960-2). Overlay histogram showing K562 cells stained with A01960-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSIP1 Antibody (A01960-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-dnajc5-picoband-trade-antibody-a04220-2-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04220-2-dnajc5-primary-antibodies-wb-testing-1_1.jpgAnti-DNAJC5 Antibody Picoband®Western blot analysis of DNAJC5 using anti-DNAJC5 antibody (A04220-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human CACO-2 whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJC5 antigen affinity purified polyclonal antibody (A04220-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNAJC5 at approximately 24 kDa. The expected band size for DNAJC5 is at 22 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-plod1-picoband-trade-antibody-a05322-1-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05322-1-plod1-primary-antibodies-wb-testing-1.jpgAnti-PLOD1 Antibody Picoband® Western blot analysis of PLOD1 using anti-PLOD1 antibody (A05322-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U87 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLOD1 antigen affinity purified polyclonal antibody (Catalog # A05322-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLOD1 at approximately 84 kDa. The expected band size for PLOD1 is at 84 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-wdr5-picoband-trade-antibody-a01910-3-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01910-3-wdr5ab-primary-antibodies-wb-testing-1.jpgAnti-WDR5 Antibody Picoband® Western blot analysis of WDR5 using anti-WDR5 antibody (A01910-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-WDR5 antigen affinity purified polyclonal antibody (Catalog # A01910-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for WDR5 at approximately 37 kDa. The expected band size for WDR5 is at 37 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-ahrr-picoband-trade-antibody-a01515-3-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-wb-testing-1.jpgAnti-AHRR Antibody Picoband® Western blot analysis of AHRR using anti-AHRR antibody (A01515-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AHRR antigen affinity purified polyclonal antibody (Catalog # A01515-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AHRR at approximately 100 kDa. The expected band size for AHRR is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-ihc-testing-2.jpgAnti-AHRR Antibody Picoband® IHC analysis of AHRR using anti-AHRR antibody (A01515-3). AHRR was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHRR Antibody (A01515-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-ihc-testing-3.jpgAnti-AHRR Antibody Picoband® IHC analysis of AHRR using anti-AHRR antibody (A01515-3). AHRR was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHRR Antibody (A01515-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-ihc-testing-4.jpgAnti-AHRR Antibody Picoband® IHC analysis of AHRR using anti-AHRR antibody (A01515-3). AHRR was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHRR Antibody (A01515-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-ihc-testing-5.jpgAnti-AHRR Antibody Picoband® IHC analysis of AHRR using anti-AHRR antibody (A01515-3). AHRR was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHRR Antibody (A01515-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-ihc-testing-6.jpgAnti-AHRR Antibody Picoband® IHC analysis of AHRR using anti-AHRR antibody (A01515-3). AHRR was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHRR Antibody (A01515-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-ihc-testing-7.jpgAnti-AHRR Antibody Picoband® IHC analysis of AHRR using anti-AHRR antibody (A01515-3). AHRR was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHRR Antibody (A01515-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-ihc-testing-8.jpgAnti-AHRR Antibody Picoband® IHC analysis of AHRR using anti-AHRR antibody (A01515-3). AHRR was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AHRR Antibody (A01515-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-if-testing-9.jpgAnti-AHRR Antibody Picoband® IF analysis of AHRR using anti-AHRR antibody (A01515-3) and anti-Beta Tubulin antibody (M01857-3). AHRR was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-AHRR Antibody (A01515-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01515-3-ahrr-primary-antibodies-fcm-testing-10.pngAnti-AHRR Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-AHRR antibody (A01515-3). Overlay histogram showing HEL cells stained with A01515-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-AHRR Antibody (A01515-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-atp5f1d-picoband-trade-antibody-a32272-2-boster.html2026-03-16T09:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-wb-testing-1.jpgAnti-ATP5F1D Antibody Picoband® Western blot analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Raji whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP5D/ATP5F1D antigen affinity purified polyclonal antibody (Catalog # A32272-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP5D/ATP5F1D at approximately 17 kDa. The expected band size for ATP5D/ATP5F1D is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-ihc-testing-2.jpgAnti-ATP5F1D Antibody Picoband® IHC analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-ihc-testing-3.jpgAnti-ATP5F1D Antibody Picoband® IHC analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-ihc-testing-4.jpgAnti-ATP5F1D Antibody Picoband® IHC analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-ihc-testing-5.jpgAnti-ATP5F1D Antibody Picoband® IHC analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-ihc-testing-6.jpgAnti-ATP5F1D Antibody Picoband® IHC analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-ihc-testing-7.jpgAnti-ATP5F1D Antibody Picoband® IHC analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-ihc-testing-8.jpgAnti-ATP5F1D Antibody Picoband® IHC analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32272-2-atp5f1d-primary-antibodies-if-testing-9.jpgAnti-ATP5F1D Antibody Picoband® IF analysis of ATP5D/ATP5F1D using anti-ATP5D/ATP5F1D antibody (A32272-2). ATP5D/ATP5F1D was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ATP5D/ATP5F1D Antibody (A32272-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-lrch4-picoband-trade-antibody-a13633-1-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13633-1-lrch4-primary-antibodies-wb-testing-1.jpgAnti-LRCH4 Antibody Picoband® Western blot analysis of LRCH4 using anti-LRCH4 antibody (A13633-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human Caco-2 whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRCH4 antigen affinity purified polyclonal antibody (Catalog # A13633-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRCH4 at approximately 84 kDa. The expected band size for LRCH4 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13633-1-lrch4-primary-antibodies-fcm-testing-2.pngAnti-LRCH4 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-LRCH4 antibody (A13633-1). Overlay histogram showing JK cells stained with A13633-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRCH4 Antibody (A13633-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lap3-picoband-trade-antibody-a01921-1-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01921-1-lap3-primary-antibodies-wb-testing-1.jpgAnti-LAP3 Antibody Picoband® Western blot analysis of LAP3 using anti-LAP3 antibody (A01921-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LAP3 antigen affinity purified polyclonal antibody (Catalog # A01921-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LAP3 at approximately 56 kDa. The expected band size for LAP3 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01921-1-lap3-primary-antibodies-ihc-testing-2.jpgAnti-LAP3 Antibody Picoband® IHC analysis of LAP3 using anti-LAP3 antibody (A01921-1). LAP3 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LAP3 Antibody (A01921-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01921-1-lap3-primary-antibodies-ihc-testing-3.jpgAnti-LAP3 Antibody Picoband® IHC analysis of LAP3 using anti-LAP3 antibody (A01921-1). LAP3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LAP3 Antibody (A01921-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01921-1-lap3-primary-antibodies-if-testing-4.jpgAnti-LAP3 Antibody Picoband® IF analysis of LAP3 using anti-LAP3 antibody (A01921-1). LAP3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LAP3 Antibody (A01921-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-lhpp-picoband-trade-antibody-a10687-boster.html2026-03-17T05:15:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10687-lhpp-primary-antibodies-wb-testing-1.jpgAnti-LHPP Antibody Picoband® Western blot analysis of LHPP using anti-LHPP antibody (A10687). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: human Hacat whole cell lysates, Lane 6: human MCF-7 whole cell lysates, Lane 7: human HEL whole cell lysates, Lane 8: rat RH35 whole cell lysates, Lane 9: mouse HEPA1/6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LHPP antigen affinity purified polyclonal antibody (Catalog # A10687) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LHPP at approximately 29 kDa. The expected band size for LHPP is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10687-lhpp-primary-antibodies-if-testing-2.jpgAnti-LHPP Antibody Picoband® IF analysis of LHPP using anti-LHPP antibody (A10687). LHPP was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LHPP Antibody (A10687) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10687-lhpp-primary-antibodies-fcm-testing-3.pngAnti-LHPP Antibody Picoband® Flow Cytometry analysis of JK cells using anti-LHPP antibody (A10687). Overlay histogram showing JK cells stained with A10687 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LHPP Antibody (A10687, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrit3-picoband-trade-antibody-a10719-1-boster.html2026-03-16T09:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10719-1-lrit3-primary-antibodies-wb-testing-1.jpgAnti-LRIT3 Antibody Picoband® Western blot analysis of LRIT3 using anti-LRIT3 antibody (A10719-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRIT3 antigen affinity purified polyclonal antibody (Catalog # A10719-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRIT3 at approximately 75 kDa. The expected band size for LRIT3 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10719-1-lrit3-primary-antibodies-if-testing-2.jpgAnti-LRIT3 Antibody Picoband® IF analysis of LRIT3 using anti-LRIT3 antibody (A10719-1) and anti-Beta Tubulin antibody (M01857-3). LRIT3 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LRIT3 Antibody (A10719-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-lrrc47-picoband-trade-antibody-a14623-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14623-1-lrrc47-primary-antibodies-wb-testing-1.jpgAnti-LRRC47 Antibody Picoband® Western blot analysis of LRRC47 using anti-LRRC47 antibody (A14623-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human K562 whole cell lysates, Lane 7: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC47 antigen affinity purified polyclonal antibody (Catalog # A14623-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC47 at approximately 68 kDa. The expected band size for LRRC47 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14623-1-lrrc47-primary-antibodies-fcm-testing-2.pngAnti-LRRC47 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-LRRC47 antibody (A14623-1). Overlay histogram showing HEL cells stained with A14623-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRC47 Antibody (A14623-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrrc59-picoband-trade-antibody-a09874-2-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-wb-testing-1.jpgAnti-LRRC59 Antibody Picoband® Western blot analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: human Caco-2 whole cell lysates, Lane 6: human A431 whole cell lysates, Lane 7: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC59 antigen affinity purified polyclonal antibody (Catalog # A09874-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC59 at approximately 35 kDa. The expected band size for LRRC59 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-wb-testing-2.jpgAnti-LRRC59 Antibody Picoband® Western blot analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat RH-35 whole cell lysates, Lane 3: mouse liver tissue lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC59 antigen affinity purified polyclonal antibody (Catalog # A09874-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC59 at approximately 35 kDa. The expected band size for LRRC59 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-ihc-testing-3.jpgAnti-LRRC59 Antibody Picoband® IHC analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). LRRC59 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC59 Antibody (A09874-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-ihc-testing-4.jpgAnti-LRRC59 Antibody Picoband® IHC analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). LRRC59 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC59 Antibody (A09874-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-ihc-testing-5.jpgAnti-LRRC59 Antibody Picoband® IHC analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). LRRC59 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC59 Antibody (A09874-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-ihc-testing-6.jpgAnti-LRRC59 Antibody Picoband® IHC analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). LRRC59 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC59 Antibody (A09874-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-ihc-testing-7.jpgAnti-LRRC59 Antibody Picoband® IHC analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). LRRC59 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC59 Antibody (A09874-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-if-testing-8.jpgAnti-LRRC59 Antibody Picoband® IF analysis of LRRC59 using anti-LRRC59 antibody (A09874-2). LRRC59 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LRRC59 Antibody (A09874-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09874-2-lrrc59-primary-antibodies-fcm-testing-9.pngAnti-LRRC59 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-LRRC59 antibody (A09874-2). Overlay histogram showing JK cells stained with A09874-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRC59 Antibody (A09874-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrrc73-picoband-trade-antibody-a18460-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18460-1-lrrc73-primary-antibodies-wb-testing-1.jpgAnti-LRRC73 Antibody Picoband® Western blot analysis of LRRC73 using anti-LRRC73 antibody (A18460-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC73 antigen affinity purified polyclonal antibody (Catalog # A18460-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC73 at approximately 42 kDa. The expected band size for LRRC73 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18460-1-lrrc73-primary-antibodies-if-testing-2.jpgAnti-LRRC73 Antibody Picoband® IF analysis of LRRC73 using anti-LRRC73 antibody (A18460-1). LRRC73 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LRRC73 Antibody (A18460-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18460-1-lrrc73-primary-antibodies-fcm-testing-3.pngAnti-LRRC73 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-LRRC73 antibody (A18460-1). Overlay histogram showing 293T cells stained with A18460-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRC73 Antibody (A18460-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrrc75a-picoband-trade-antibody-a18461-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18461-1-lrrc75a-primary-antibodies-wb-testing-1.jpgAnti-LRRC75A Antibody Picoband® Western blot analysis of LRRC75A using anti-LRRC75A antibody (A18461-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC75A antigen affinity purified polyclonal antibody (Catalog # A18461-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC75A at approximately 36 kDa. The expected band size for LRRC75A is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18461-1-lrrc75a-primary-antibodies-fcm-testing-2.pngAnti-LRRC75A Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-LRRC75A antibody (A18461-1). Overlay histogram showing HEL cells stained with A18461-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRC75A Antibody (A18461-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrrc75b-picoband-trade-antibody-a18683-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18683-1-lrrc75b-primary-antibodies-wb-testing-1.jpgAnti-LRRC75B Antibody Picoband® Western blot analysis of LRRC75B using anti-LRRC75B antibody (A18683-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC75B antigen affinity purified polyclonal antibody (Catalog # A18683-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC75B at approximately 35 kDa. The expected band size for LRRC75B is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18683-1-lrrc75b-primary-antibodies-ihc-testing-2.jpgAnti-LRRC75B Antibody Picoband® IHC analysis of LRRC75B using anti-LRRC75B antibody (A18683-1). LRRC75B was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC75B Antibody (A18683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18683-1-lrrc75b-primary-antibodies-ihc-testing-3.jpgAnti-LRRC75B Antibody Picoband® IHC analysis of LRRC75B using anti-LRRC75B antibody (A18683-1). LRRC75B was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC75B Antibody (A18683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18683-1-lrrc75b-primary-antibodies-ihc-testing-4.jpgAnti-LRRC75B Antibody Picoband® IHC analysis of LRRC75B using anti-LRRC75B antibody (A18683-1). LRRC75B was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRC75B Antibody (A18683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18683-1-lrrc75b-primary-antibodies-fcm-testing-5.pngAnti-LRRC75B Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-LRRC75B antibody (A18683-1). Overlay histogram showing PC-3 cells stained with A18683-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRC75B Antibody (A18683-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrrn1-picoband-trade-antibody-a12074-1-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12074-1-lrrn1-primary-antibodies-wb-testing-1.jpgAnti-LRRN1 Antibody Picoband® Western blot analysis of LRRN1 using anti-LRRN1 antibody (A12074-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skeletal muscle tissue lysates, Lane 2: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRN1 antigen affinity purified polyclonal antibody (Catalog # A12074-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRN1 at approximately 95 kDa. The expected band size for LRRN1 is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12074-1-lrrn1-primary-antibodies-ihc-testing-2.jpgAnti-LRRN1 Antibody Picoband® IHC analysis of LRRN1 using anti-LRRN1 antibody (A12074-1). LRRN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRN1 Antibody (A12074-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12074-1-lrrn1-primary-antibodies-fcm-testing-3.pngAnti-LRRN1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-LRRN1 antibody (A12074-1). Overlay histogram showing SH-SY5Y cells stained with A12074-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRN1 Antibody (A12074-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrrn4-picoband-trade-antibody-a15151-2-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15151-2-lrrn4-primary-antibodies-wb-testing-1.jpgAnti-LRRN4 Antibody Picoband® Western blot analysis of LRRN4 using anti-LRRN4 antibody (A15151-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRN4 antigen affinity purified polyclonal antibody (Catalog # A15151-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRN4 at approximately 79 kDa. The expected band size for LRRN4 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15151-2-lrrn4-primary-antibodies-ihc-testing-2.jpgAnti-LRRN4 Antibody Picoband® IHC analysis of LRRN4 using anti-LRRN4 antibody (A15151-2). LRRN4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRN4 Antibody (A15151-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15151-2-lrrn4-primary-antibodies-ihc-testing-3.jpgAnti-LRRN4 Antibody Picoband® IHC analysis of LRRN4 using anti-LRRN4 antibody (A15151-2). LRRN4 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRN4 Antibody (A15151-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15151-2-lrrn4-primary-antibodies-ihc-testing-4.jpgAnti-LRRN4 Antibody Picoband® IHC analysis of LRRN4 using anti-LRRN4 antibody (A15151-2). LRRN4 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LRRN4 Antibody (A15151-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15151-2-lrrn4-primary-antibodies-if-testing-5.jpgAnti-LRRN4 Antibody Picoband® IF analysis of LRRN4 using anti-LRRN4 antibody (A15151-2). LRRN4 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LRRN4 Antibody (A15151-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15151-2-lrrn4-primary-antibodies-fcm-testing-6.pngAnti-LRRN4 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-LRRN4 antibody (A15151-2). Overlay histogram showing U20S cells stained with A15151-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRN4 Antibody (A15151-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ldhd-picoband-trade-antibody-a11154-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11154-1-ldhd-primary-antibodies-wb-testing-1.jpgAnti-LDHD Antibody Picoband® Western blot analysis of LDHD using anti-LDHD antibody (A11154-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LDHD antigen affinity purified polyclonal antibody (Catalog # A11154-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LDHD at approximately 45-50 kDa. The expected band size for LDHD is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11154-1-ldhd-primary-antibodies-fcm-testing-2.pngAnti-LDHD Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-LDHD antibody (A11154-1). Overlay histogram showing K562 cells stained with A11154-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LDHD Antibody (A11154-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-fbxo32-picoband-trade-antibody-a02531-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02531-1-fbxo32-primary-antibodies-wb-testing-1.jpgAnti-FBXO32 Antibody Picoband® Western blot analysis of Fbx32/FBXO32 using anti-Fbx32/FBXO32 antibody (A02531-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse heart tissue lysates, Lane 2: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Fbx32/FBXO32 antigen affinity purified polyclonal antibody (Catalog # A02531-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Fbx32/FBXO32 at approximately 42 kDa. The expected band size for Fbx32/FBXO32 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02531-1-fbxo32-primary-antibodies-if-testing-2.jpgAnti-FBXO32 Antibody Picoband® IF analysis of Fbx32/FBXO32 using anti-Fbx32/FBXO32 antibody (A02531-1) and anti-Beta Tubulin antibody (M01857-3). Fbx32/FBXO32 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Fbx32/FBXO32 Antibody (A02531-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02531-1-fbxo32-primary-antibodies-fcm-testing-3.pngAnti-FBXO32 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-Fbx32/FBXO32 antibody (A02531-1). Overlay histogram showing PC-3 cells stained with A02531-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Fbx32/FBXO32 Antibody (A02531-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lcmt2-picoband-trade-antibody-a14797-1-boster.html2026-03-16T09:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14797-1-lcmt2-primary-antibodies-wb-testing-1.jpgAnti-LCMT2 Antibody Picoband® Western blot analysis of LCMT2 using anti-LCMT2 antibody (A14797-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LCMT2 antigen affinity purified polyclonal antibody (Catalog # A14797-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LCMT2 at approximately 76 kDa. The expected band size for LCMT2 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14797-1-lcmt2-primary-antibodies-if-testing-2.jpgAnti-LCMT2 Antibody Picoband® IF analysis of LCMT2 using anti-LCMT2 antibody (A14797-1). LCMT2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LCMT2 Antibody (A14797-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-ltb-picoband-trade-antibody-a02565-2-boster.html2026-04-05T05:00:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02565-2-ltb-primary-antibodies-wb-testing-1.jpgAnti-Ltb Antibody Picoband® Western blot analysis of Ltb using anti-Ltb antibody (A02565-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat PC-12 whole cell lysates, Lane 2: mouse spleen tissue lysates, Lane 3: mouse thymus tissue lysates, Lane 4: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ltb antigen affinity purified polyclonal antibody (Catalog # A02565-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Ltb at approximately 25 kDa. The expected band size for Ltb is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02565-2-ltb-primary-antibodies-fcm-testing-2.pngAnti-Ltb Antibody Picoband® Flow Cytometry analysis of RAW264.7 cells using anti-Ltb antibody (A02565-2). Overlay histogram showing RAW264.7 cells stained with A02565-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Ltb Antibody (A02565-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-crop-luc7l3-picoband-trade-antibody-a08633-3-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-wb-testing-1.jpgAnti-CROP/LUC7L3 Antibody Picoband® Western blot analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CROP/LUC7L3 antigen affinity purified polyclonal antibody (Catalog # A08633-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CROP/LUC7L3 at approximately 55 kDa. The expected band size for CROP/LUC7L3 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-2.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of human highly differentiated adenocarcinoma of the colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-3.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of human large B-cell lymphoma of the colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-4.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-5.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-6.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-7.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-8.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-9.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-10.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-ihc-testing-11.jpgAnti-CROP/LUC7L3 Antibody Picoband® IHC analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3). CROP/LUC7L3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CROP/LUC7L3 Antibody (A08633-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-if-testing-12.jpgAnti-CROP/LUC7L3 Antibody Picoband® IF analysis of CROP/LUC7L3 using anti-CROP/LUC7L3 antibody (A08633-3) and anti-Beta Tubulin antibody (M01857-3). CROP/LUC7L3 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CROP/LUC7L3 Antibody (A08633-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08633-3-luc7l3-primary-antibodies-fcm-testing-13.pngAnti-CROP/LUC7L3 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-CROP/LUC7L3 antibody (A08633-3). Overlay histogram showing JK cells stained with A08633-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CROP/LUC7L3 Antibody (A08633-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rrbp1-picoband-trade-antibody-a07074-2-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07074-2-rrbp1-primary-antibodies-wb-testing-1.jpgAnti-RRBP1 Antibody Picoband® Western blot analysis of RRBP1 using anti-RRBP1 antibody (A07074-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RRBP1 antigen affinity purified polyclonal antibody (Catalog # A07074-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RRBP1 at approximately 190-200 kDa. The expected band size for RRBP1 is at 152 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07074-2-rrbp1-primary-antibodies-ihc-testing-2.jpgAnti-RRBP1 Antibody Picoband® IHC analysis of RRBP1 using anti-RRBP1 antibody (A07074-2). RRBP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RRBP1 Antibody (A07074-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07074-2-rrbp1-primary-antibodies-ihc-testing-3.jpgAnti-RRBP1 Antibody Picoband® IHC analysis of RRBP1 using anti-RRBP1 antibody (A07074-2). RRBP1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RRBP1 Antibody (A07074-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07074-2-rrbp1-primary-antibodies-if-testing-4.jpgAnti-RRBP1 Antibody Picoband® IF analysis of RRBP1 using anti-RRBP1 antibody (A07074-2). RRBP1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RRBP1 Antibody (A07074-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07074-2-rrbp1-primary-antibodies-fcm-testing-5.pngAnti-RRBP1 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-RRBP1 antibody (A07074-2). Overlay histogram showing U20S cells stained with A07074-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RRBP1 Antibody (A07074-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-neuropilin-1-nrp1-picoband-trade-antibody-a01324-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01324-1-nrp1-primary-antibodies-wb-testing-1.jpgAnti-Neuropilin 1/NRP1 Antibody Picoband® Western blot analysis of Neuropilin 1/NRP1 using anti-Neuropilin 1/NRP1 antibody (A01324-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Neuropilin 1/NRP1 antigen affinity purified polyclonal antibody (Catalog # A01324-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Neuropilin 1/NRP1 at approximately 140 kDa. The expected band size for Neuropilin 1/NRP1 is at 103 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-rab14-picoband-trade-antibody-a04231-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04231-1-rab14-primary-antibodies-wb-testing-1.jpgAnti-RAB14 Antibody Picoband® Western blot analysis of RAB14 using anti-RAB14 antibody (A04231-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human T-47D whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: human A431 whole cell lysates, Lane 6: human U937 whole cell lysates, Lane 7: human MCF-7 whole cell lysates, Lane 8: rat brain tissue lysates, Lane 9: mouse brain tissue lysates, Lane 10: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB14 antigen affinity purified polyclonal antibody (Catalog # A04231-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAB14 at approximately 24 kDa. The expected band size for RAB14 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04231-1-rab14-primary-antibodies-fcm-testing-2.pngAnti-RAB14 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-RAB14 antibody (A04231-1). Overlay histogram showing Hela cells stained with A04231-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAB14 Antibody (A04231-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-palmd-picoband-trade-antibody-a11148-1-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11148-palmd-primary-antibodies-wb-testing-1.jpgAnti-PALMD Antibody Picoband® Western blot analysis of PALMD using anti-PALMD antibody (A11148-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PALMD antigen affinity purified polyclonal antibody (Catalog # A11148-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PALMD at approximately 68 kDa. The expected band size for PALMD is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11148-palmd-primary-antibodies-fcm-testing-2.pngAnti-PALMD Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PALMD antibody (A11148). Overlay histogram showing Hela cells stained with A11148 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PALMD Antibody (A11148, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mip-3-beta-ccl19-picoband-trade-antibody-a01605-2-boster.html2026-03-16T09:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01605-2-ccl9-primary-antibodies-ihc-testing-1.jpgAnti-MIP-3 Beta/CCL19 Antibody IHC analysis of MIP-3 Beta/CCL19 using anti-MIP-3 Beta/CCL19 antibody (A01605-2). MIP-3 Beta/CCL19 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIP-3 Beta/CCL19 Antibody (A01605-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01605-2-ccl9-primary-antibodies-fcm-testing-2.pngAnti-MIP-3 Beta/CCL19 Antibody Flow Cytometry analysis of THP-1 cells using anti-MIP-3 Beta/CCL19 antibody (A01605-2). Overlay histogram showing THP-1 cells stained with A01605-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MIP-3 Beta/CCL19 Antibody (A01605-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-sqh-antibody-dz41457-boster.html2026-04-03T05:00:53+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-annual-killifish-caprin-1-isoform-x3-dz41458-boster.html2026-03-10T04:36:43+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-alpha-1b-glycoprotein-a1bg-picoband-trade-antibody-a07289-2-boster.html2026-03-17T05:15:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07289-2-a1bg-primary-antibodies-wb-testing-1.jpgAnti-Alpha 1B-Glycoprotein/A1BG Antibody Picoband® Western blot analysis of Alpha 1B-Glycoprotein/A1BG using anti-Alpha 1B-Glycoprotein/A1BG antibody (A07289-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates, Lane 2: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 3: rat plasma lysates, Lane 4: mouse plasma lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Alpha 1B-Glycoprotein/A1BG antigen affinity purified polyclonal antibody (Catalog # A07289-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Alpha 1B-Glycoprotein/A1BG at approximately 50-75 kDa. The expected band size for Alpha 1B-Glycoprotein/A1BG is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07289-2-a1bg-primary-antibodies-fcm-testing-2.pngAnti-Alpha 1B-Glycoprotein/A1BG Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Alpha 1B-Glycoprotein/A1BG antibody (A07289-2). Overlay histogram showing HepG2 cells stained with A07289-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Alpha 1B-Glycoprotein/A1BG Antibody (A07289-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-neurod2-picoband-trade-antibody-a07904-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07904-1-neurod2-primary-antibodies-wb-testing-1.jpgAnti-NEUROD2 Antibody Picoband® Western blot analysis of NEUROD2 using anti-NEUROD2 antibody (A07904-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NEUROD2 antigen affinity purified polyclonal antibody (Catalog # A07904-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NEUROD2 at approximately 50 kDa. The expected band size for NEUROD2 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07904-1-neurod2-primary-antibodies-fcm-testing-2.pngAnti-NEUROD2 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NEUROD2 antibody (A07904-1). Overlay histogram showing 293T cells stained with A07904-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NEUROD2 Antibody (A07904-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mtf1-picoband-trade-antibody-a04733-3-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04733-3-mtf1-primary-antibodies-wb-testing-1.jpgAnti-MTF1 Antibody Picoband® Western blot analysis of MTF1 using anti-MTF1 antibody (A04733-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat brain tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTF1 antigen affinity purified polyclonal antibody (Catalog # A04733-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MTF1 at approximately 65 kDa. The expected band size for MTF1 is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04733-3-mtf1-primary-antibodies-ihc-testing-2.jpgAnti-MTF1 Antibody Picoband® IHC analysis of MTF1 using anti-MTF1 antibody (A04733-3). MTF1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTF1 Antibody (A04733-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04733-3-mtf1-primary-antibodies-ihc-testing-3.jpgAnti-MTF1 Antibody Picoband® IHC analysis of MTF1 using anti-MTF1 antibody (A04733-3). MTF1 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTF1 Antibody (A04733-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04733-3-mtf1-primary-antibodies-if-testing-4.jpgAnti-MTF1 Antibody Picoband® IF analysis of MTF1 using anti-MTF1 antibody (A04733-3). MTF1 was detected in an immunocytochemical section of U87 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MTF1 Antibody (A04733-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04733-3-mtf1-primary-antibodies-fcm-testing-5.pngAnti-MTF1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MTF1 antibody (A04733-3). Overlay histogram showing 293T cells stained with A04733-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MTF1 Antibody (A04733-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mutyh-picoband-trade-antibody-a01618-2-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01618-2-mutyh-primary-antibodies-wb-testing-1.jpgAnti-MUTYH Antibody Picoband® Western blot analysis of MUTYH using anti-MUTYH antibody (A01618-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MUTYH antigen affinity purified polyclonal antibody (Catalog # A01618-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MUTYH at approximately 60 kDa. The expected band size for MUTYH is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01618-2-mutyh-primary-antibodies-fcm-testing-2.pngAnti-MUTYH Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MUTYH antibody (A01618-2). Overlay histogram showing Hela cells stained with A01618-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MUTYH Antibody (A01618-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pdk4-picoband-trade-antibody-a02132-1-boster.html2026-03-16T09:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02132-1-pdk4-primary-antibodies-wb-testing-1.jpgAnti-PDK4 Antibody Picoband® Western blot analysis of PDK4 using anti-PDK4 antibody (A02132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDK4 antigen affinity purified polyclonal antibody (Catalog # A02132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDK4 at approximately 46 kDa. The expected band size for PDK4 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02132-1-pdk4-primary-antibodies-ihc-testing-2.jpgAnti-PDK4 Antibody Picoband® IHC analysis of PDK4 using anti-PDK4 antibody (A02132-1). PDK4 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDK4 Antibody (A02132-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02132-1-pdk4-primary-antibodies-if-testing-3.jpgAnti-PDK4 Antibody Picoband® IF analysis of PDK4 using anti-PDK4 antibody (A02132-1). PDK4 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PDK4 Antibody (A02132-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02132-1-pdk4-primary-antibodies-if-testing-4.jpgAnti-PDK4 Antibody Picoband® IF analysis of PDK4 using anti-PDK4 antibody (A02132-1). PDK4 was detected in a paraffin-embedded section of human squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PDK4 Antibody (A02132-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02132-1-pdk4-primary-antibodies-fcm-testing-5.pngAnti-PDK4 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PDK4 antibody (A02132-1). Overlay histogram showing Hela cells stained with A02132-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDK4 Antibody (A02132-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-palm-picoband-trade-antibody-a00265-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00265-1-palm-primary-antibodies-wb-testing-1.jpgAnti-PALM Antibody Picoband® Western blot analysis of PALM using anti-PALM antibody (A00265-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PALM antigen affinity purified polyclonal antibody (Catalog # A00265-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PALM at approximately 37 kDa. The expected band size for PALM is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00265-1-palm-primary-antibodies-ihc-testing-2.jpgAnti-PALM Antibody Picoband® IHC analysis of PALM using anti-PALM antibody (A00265-1). PALM was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PALM Antibody (A00265-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00265-1-palm-primary-antibodies-ihc-testing-3.jpgAnti-PALM Antibody Picoband® IHC analysis of PALM using anti-PALM antibody (A00265-1). PALM was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PALM Antibody (A00265-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0003) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00265-1-palm-primary-antibodies-ihc-testing-4.jpgAnti-PALM Antibody Picoband® IHC analysis of PALM using anti-PALM antibody (A00265-1). PALM was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PALM Antibody (A00265-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0003) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00265-1-palm-primary-antibodies-ihc-testing-5.jpgAnti-PALM Antibody Picoband® IHC analysis of PALM using anti-PALM antibody (A00265-1). PALM was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PALM Antibody (A00265-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0003) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00265-1-palm-primary-antibodies-ihc-testing-6.jpgAnti-PALM Antibody Picoband® IHC analysis of PALM using anti-PALM antibody (A00265-1). PALM was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PALM Antibody (A00265-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0003) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00265-1-palm-primary-antibodies-fcm-testing-7.pngAnti-PALM Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PALM antibody (A00265-1). Overlay histogram showing SH-SY5Y cells stained with A00265-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PALM Antibody (A00265-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lsg1-picoband-trade-antibody-a10338-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10338-1-lsg1-primary-antibodies-wb-testing-1.jpgAnti-LSG1 Antibody Picoband® Western blot analysis of LSG1 using anti-LSG1 antibody (A10338-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: human RT4 whole cell lysates, Lane 6: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LSG1 antigen affinity purified polyclonal antibody (Catalog # A10338-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LSG1 at approximately 75-80 kDa. The expected band size for LSG1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10338-1-lsg1-primary-antibodies-ihc-testing-2.jpgAnti-LSG1 Antibody Picoband® IHC analysis of LSG1 using anti-LSG1 antibody (A10338-1). LSG1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LSG1 Antibody (A10338-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10338-1-lsg1-primary-antibodies-ihc-testing-3.jpgAnti-LSG1 Antibody Picoband® IHC analysis of LSG1 using anti-LSG1 antibody (A10338-1). LSG1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LSG1 Antibody (A10338-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10338-1-lsg1-primary-antibodies-if-testing-4.jpgAnti-LSG1 Antibody Picoband® IF analysis of LSG1 using anti-LSG1 antibody (A10338-1). LSG1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LSG1 Antibody (A10338-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10338-1-lsg1-primary-antibodies-fcm-testing-5.pngAnti-LSG1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-LSG1 antibody (A10338-1). Overlay histogram showing RT4 cells stained with A10338-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LSG1 Antibody (A10338-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lta4h-picoband-trade-antibody-a02399-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02399-1-lta4h-primary-antibodies-wb-testing-1.jpgAnti-LTA4H Antibody Picoband® Western blot analysis of LTA4H using anti-LTA4H antibody (A02399-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: human PC-3 whole cell lysates, Lane 7: rat thymus tissue lysates, Lane 8: rat C6 whole cell lysates, Lane 9: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LTA4H antigen affinity purified polyclonal antibody (Catalog # A02399-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LTA4H at approximately 69 kDa. The expected band size for LTA4H is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02399-1-lta4h-primary-antibodies-ihc-testing-2.jpgAnti-LTA4H Antibody Picoband® IHC analysis of LTA4H using anti-LTA4H antibody (A02399-1). LTA4H was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LTA4H Antibody (A02399-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02399-1-lta4h-primary-antibodies-ihc-testing-3.jpgAnti-LTA4H Antibody Picoband® IHC analysis of LTA4H using anti-LTA4H antibody (A02399-1). LTA4H was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LTA4H Antibody (A02399-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02399-1-lta4h-primary-antibodies-ihc-testing-4.jpgAnti-LTA4H Antibody Picoband® IHC analysis of LTA4H using anti-LTA4H antibody (A02399-1). LTA4H was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LTA4H Antibody (A02399-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02399-1-lta4h-primary-antibodies-ihc-testing-5.jpgAnti-LTA4H Antibody Picoband® IHC analysis of LTA4H using anti-LTA4H antibody (A02399-1). LTA4H was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LTA4H Antibody (A02399-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02399-1-lta4h-primary-antibodies-if-testing-6.jpgAnti-LTA4H Antibody Picoband® IF analysis of LTA4H using anti-LTA4H antibody (A02399-1). LTA4H was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-LTA4H Antibody (A02399-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02399-1-lta4h-primary-antibodies-fcm-testing-7.pngAnti-LTA4H Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-LTA4H antibody (A02399-1). Overlay histogram showing RT4 cells stained with A02399-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LTA4H Antibody (A02399-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-luc7l-picoband-trade-antibody-a10943-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10943-1-luc7l-primary-antibodies-wb-testing-1.jpgAnti-LUC7L Antibody Picoband® Western blot analysis of LUC7L using anti-LUC7L antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LUC7L antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LUC7L at approximately 44 kDa. The expected band size for LUC7L is at 44 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-lumican-lum-picoband-trade-antibody-a01034-2-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01034-2-lum-primary-antibodies-wb-testing-1.jpgAnti-Lumican/LUM Antibody Picoband® Western blot analysis of Lumican/LUM using anti-Lumican/LUM antibody (A01034-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human placenta tissue lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lumican/LUM antigen affinity purified polyclonal antibody (Catalog # A01034-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lumican/LUM at approximately 70 kDa. The expected band size for Lumican/LUM is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01034-2-lum-primary-antibodies-ihc-testing-2.jpgAnti-Lumican/LUM Antibody Picoband® IHC analysis of Lumican/LUM using anti-Lumican/LUM antibody (A01034-2). Lumican/LUM was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lumican/LUM Antibody (A01034-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01034-2-lum-primary-antibodies-ihc-testing-3.jpgAnti-Lumican/LUM Antibody Picoband® IHC analysis of Lumican/LUM using anti-Lumican/LUM antibody (A01034-2). Lumican/LUM was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lumican/LUM Antibody (A01034-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01034-2-lum-primary-antibodies-ihc-testing-4.jpgAnti-Lumican/LUM Antibody Picoband® IHC analysis of Lumican/LUM using anti-Lumican/LUM antibody (A01034-2). Lumican/LUM was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lumican/LUM Antibody (A01034-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01034-2-lum-primary-antibodies-ihc-testing-5.jpgAnti-Lumican/LUM Antibody Picoband® IHC analysis of Lumican/LUM using anti-Lumican/LUM antibody (A01034-2). Lumican/LUM was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lumican/LUM Antibody (A01034-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01034-2-lum-primary-antibodies-fcm-testing-6.pngAnti-Lumican/LUM Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-Lumican/LUM antibody (A01034-2). Overlay histogram showing SH-SY5Y cells stained with A01034-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Lumican/LUM Antibody (A01034-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lypd3-picoband-trade-antibody-a08396-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08396-lypd3-primary-antibodies-wb-testing-1.jpgAnti-LYPD3 Antibody Picoband® Western blot analysis of LYPD3 using anti-LYPD3 antibody (A08396). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: rat stomach tissue lysates, Lane 4: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LYPD3 antigen affinity purified polyclonal antibody (Catalog # A08396) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LYPD3 at approximately 75 kDa. The expected band size for LYPD3 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08396-lypd3-primary-antibodies-ihc-testing-2.jpgAnti-LYPD3 Antibody Picoband® IHC analysis of LYPD3 using anti-LYPD3 antibody (A08396). LYPD3 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPD3 Antibody (A08396) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08396-lypd3-primary-antibodies-ihc-testing-3.jpgAnti-LYPD3 Antibody Picoband® IHC analysis of LYPD3 using anti-LYPD3 antibody (A08396). LYPD3 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPD3 Antibody (A08396) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08396-lypd3-primary-antibodies-if-testing-4.jpgAnti-LYPD3 Antibody Picoband® IF analysis of LYPD3 using anti-LYPD3 antibody (A08396). LYPD3 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-LYPD3 Antibody (A08396) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08396-lypd3-primary-antibodies-fcm-testing-5.pngAnti-LYPD3 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-LYPD3 antibody (A08396). Overlay histogram showing RT4 cells stained with A08396 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LYPD3 Antibody (A08396, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lypd6-picoband-trade-antibody-a08243-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08243-1-lypd6-primary-antibodies-wb-testing-1.jpgAnti-LYPD6 Antibody Picoband® Western blot analysis of LYPD6 using anti-LYPD6 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LYPD6 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LYPD6 at approximately 19 kDa. The expected band size for LYPD6 is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08243-1-lypd6-primary-antibodies-fcm-testing-2.pngAnti-LYPD6 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-LYPD6 antibody (A08243-1). Overlay histogram showing SH-SY5Y cells stained with A08243-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LYPD6 Antibody (A08243-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lypla1-picoband-trade-antibody-a07249-2-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07249-2-lypla1-primary-antibodies-wb-testing-1.jpgAnti-LYPLA1 Antibody Picoband® Western blot analysis of LYPLA1 using anti-LYPLA1 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LYPLA1 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LYPLA1 at approximately 25 kDa. The expected band size for LYPLA1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07249-2-lypla1-primary-antibodies-ihc-testing-2.jpgAnti-LYPLA1 Antibody Picoband® IHC analysis of LYPLA1 using anti-LYPLA1 antibody (A07249-2). LYPLA1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPLA1 Antibody (A07249-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07249-2-lypla1-primary-antibodies-ihc-testing-3.jpgAnti-LYPLA1 Antibody Picoband® IHC analysis of LYPLA1 using anti-LYPLA1 antibody (A07249-2). LYPLA1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPLA1 Antibody (A07249-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07249-2-lypla1-primary-antibodies-ihc-testing-4.jpgAnti-LYPLA1 Antibody Picoband® IHC analysis of LYPLA1 using anti-LYPLA1 antibody (A07249-2). LYPLA1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPLA1 Antibody (A07249-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07249-2-lypla1-primary-antibodies-fcm-testing-5.pngAnti-LYPLA1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-LYPLA1 antibody (A07249-2). Overlay histogram showing HEL cells stained with A07249-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LYPLA1 Antibody (A07249-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lypla2-picoband-trade-antibody-a10621-1-boster.html2026-04-06T05:04:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10621-1-lypla2-primary-antibodies-wb-testing-1.jpgAnti-LYPLA2 Antibody Picoband® Western blot analysis of LYPLA2 using anti-LYPLA2 antibody (A10621-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat stomach tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LYPLA2 antigen affinity purified polyclonal antibody (Catalog # A10621-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LYPLA2 at approximately 25 kDa. The expected band size for LYPLA2 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10621-1-lypla2-primary-antibodies-ihc-testing-2.jpgAnti-LYPLA2 Antibody Picoband® IHC analysis of LYPLA2 using anti-LYPLA2 antibody (A10621-1). LYPLA2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPLA2 Antibody (A10621-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10621-1-lypla2-primary-antibodies-ihc-testing-3.jpgAnti-LYPLA2 Antibody Picoband® IHC analysis of LYPLA2 using anti-LYPLA2 antibody (A10621-1). LYPLA2 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPLA2 Antibody (A10621-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10621-1-lypla2-primary-antibodies-ihc-testing-4.jpgAnti-LYPLA2 Antibody Picoband® IHC analysis of LYPLA2 using anti-LYPLA2 antibody (A10621-1). LYPLA2 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPLA2 Antibody (A10621-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10621-1-lypla2-primary-antibodies-ihc-testing-5.jpgAnti-LYPLA2 Antibody Picoband® IHC analysis of LYPLA2 using anti-LYPLA2 antibody (A10621-1). LYPLA2 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LYPLA2 Antibody (A10621-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10621-1-lypla2-primary-antibodies-if-testing-6.jpgAnti-LYPLA2 Antibody Picoband® IF analysis of LYPLA2 using anti-LYPLA2 antibody (A10621-1). LYPLA2 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LYPLA2 Antibody (A10621-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10621-1-lypla2-primary-antibodies-fcm-testing-7.pngAnti-LYPLA2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-LYPLA2 antibody (A10621-1). Overlay histogram showing HEL cells stained with A10621-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LYPLA2 Antibody (A10621-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lysozyme-lyz-picoband-trade-antibody-a01811-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01811-1-lyz-primary-antibodies-wb-testing-1.jpgAnti-Lysozyme/LYZ Antibody Picoband® Western blot analysis of Lysozyme/LYZ using anti-Lysozyme/LYZ antibody (A01811-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U937 whole cell lysates, Lane 2: rat lung tissue lysates, Lane 3: mouse lung tissue lysates, Lane 4: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lysozyme/LYZ antigen affinity purified polyclonal antibody (Catalog # A01811-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lysozyme/LYZ at approximately 15-17 kDa. The expected band size for Lysozyme/LYZ is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01811-1-lyz-primary-antibodies-fcm-testing-2.pngAnti-Lysozyme/LYZ Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Lysozyme/LYZ antibody (A01811-1). Overlay histogram showing HepG2 cells stained with A01811-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Lysozyme/LYZ Antibody (A01811-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lzic-picoband-trade-antibody-a15087-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15087-lzic-primary-antibodies-wb-testing-1.jpgAnti-LZIC Antibody Picoband® Western blot analysis of LZIC using anti-LZIC antibody (A15087). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: human HEL whole cell lysates, Lane 6: human Jurkat whole cell lysates, Lane 7: rat brain tissue lysates, Lane 8: rat thymus tissue lysates, Lane 9: mouse brain tissue lysates, Lane 10: mouse thymus tissue lysates, Lane 11: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LZIC antigen affinity purified polyclonal antibody (Catalog # A15087) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LZIC at approximately 21 kDa. The expected band size for LZIC is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15087-lzic-primary-antibodies-ihc-testing-2.jpgAnti-LZIC Antibody Picoband® IHC analysis of LZIC using anti-LZIC antibody (A15087). LZIC was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LZIC Antibody (A15087) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15087-lzic-primary-antibodies-ihc-testing-3..jpgAnti-LZIC Antibody Picoband® IHC analysis of LZIC using anti-LZIC antibody (A15087). LZIC was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LZIC Antibody (A15087) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15087-lzic-primary-antibodies-ihc-testing-4.jpgAnti-LZIC Antibody Picoband® IHC analysis of LZIC using anti-LZIC antibody (A15087). LZIC was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LZIC Antibody (A15087) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15087-lzic-primary-antibodies-if-testing-5.jpgAnti-LZIC Antibody Picoband® IF analysis of LZIC using anti-LZIC antibody (A15087) and anti-Beta Tubulin antibody (M01857-3). LZIC was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LZIC Antibody (A15087) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15087-lzic-primary-antibodies-ip-testing-1.jpgAnti-LZIC Antibody Picoband®Immunoprecipitating (IP) LZIC in PC-3 whole cell lysate. Western blot analysis of LZIC using anti-LZIC antibody (A15087); Lane 1: PC-3 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-LZIC antibody in PC-3 whole cell lysate; Lane 3: anti-LZIC antibody (2μg) + PC-3 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-LZIC antigen affinity purified polyclonal antibody (A15087) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for LZIC at approximately 21 kDa. The expected band size for LZIC is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15087-lzic-primary-antibodies-fcm-testing-6.pngAnti-LZIC Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-LZIC antibody (A15087). Overlay histogram showing 293T cells stained with A15087 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LZIC Antibody (A15087, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-phf15-jade2-picoband-trade-antibody-a12993-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12993-1-jade2-primary-antibodies-wb-testing-1.jpgAnti-PHF15/JADE2 Antibody Picoband® Western blot analysis of PHF15/JADE2 using anti-PHF15/JADE2 antibody (A12993-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF15/JADE2 antigen affinity purified polyclonal antibody (Catalog # A12993-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHF15/JADE2 at approximately 120 kDa. The expected band size for PHF15/JADE2 is at 87 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-jchain-picoband-trade-antibody-a02644-2-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02644-2-jchain-primary-antibodies-wb-testing-1.jpgAnti-JCHAIN Antibody Picoband® Western blot analysis of JCHAIN using anti-JCHAIN antibody (A02644-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat small intestine tissue lysates, Lane 2: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JCHAIN antigen affinity purified polyclonal antibody (Catalog # A02644-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for JCHAIN at approximately 23 kDa. The expected band size for JCHAIN is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02644-2-jchain-primary-antibodies-ihc-testing-2.jpgAnti-JCHAIN Antibody Picoband® IHC analysis of JCHAIN using anti-JCHAIN antibody (A02644-2). JCHAIN was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-JCHAIN Antibody (A02644-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02644-2-jchain-primary-antibodies-ihc-testing-3.jpgAnti-JCHAIN Antibody Picoband® IHC analysis of JCHAIN using anti-JCHAIN antibody (A02644-2). JCHAIN was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-JCHAIN Antibody (A02644-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02644-2-jchain-primary-antibodies-ihc-testing-4.jpgAnti-JCHAIN Antibody Picoband® IHC analysis of JCHAIN using anti-JCHAIN antibody (A02644-2). JCHAIN was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-JCHAIN Antibody (A02644-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02644-2-jchain-primary-antibodies-if-testing-5.jpgAnti-JCHAIN Antibody Picoband® IF analysis of JCHAIN using anti-JCHAIN antibody (A02644-2). JCHAIN was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-JCHAIN Antibody (A02644-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02644-2-jchain-primary-antibodies-fcm-testing-6.pngAnti-JCHAIN Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-JCHAIN antibody (A02644-2). Overlay histogram showing A431 cells stained with A02644-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-JCHAIN Antibody (A02644-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-josd2-picoband-trade-antibody-a14517-1-boster.html2026-03-17T05:15:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14517-1-josd2-primary-antibodies-wb-testing-1.jpgAnti-JOSD2 Antibody Picoband® Western blot analysis of JOSD2 using anti-JOSD2 antibody (A14517-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-JOSD2 antigen affinity purified polyclonal antibody (Catalog # A14517-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for JOSD2 at approximately 26 kDa. The expected band size for JOSD2 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14517-1-josd2-primary-antibodies-ihc-testing-2.jpgAnti-JOSD2 Antibody Picoband® IHC analysis of JOSD2 using anti-JOSD2 antibody (A14517-1). JOSD2 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-JOSD2 Antibody (A14517-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14517-1-josd2-primary-antibodies-ihc-testing-3.jpgAnti-JOSD2 Antibody Picoband® IHC analysis of JOSD2 using anti-JOSD2 antibody (A14517-1). JOSD2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-JOSD2 Antibody (A14517-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14517-1-josd2-primary-antibodies-ihc-testing-4.jpgAnti-JOSD2 Antibody Picoband® IHC analysis of JOSD2 using anti-JOSD2 antibody (A14517-1). JOSD2 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-JOSD2 Antibody (A14517-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14517-1-josd2-primary-antibodies-fcm-testing-5.pngAnti-JOSD2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-JOSD2 antibody (A14517-1). Overlay histogram showing HEL cells stained with A14517-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-JOSD2 Antibody (A14517-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-iah1-picoband-trade-antibody-a14534-1-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14534-1-iah1-primary-antibodies-wb-testing-1.jpgAnti-IAH1 Antibody Picoband® Western blot analysis of IAH1 using anti-IAH1 antibody (A14534-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse kidney tissue lysates, Lane 4: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IAH1 antigen affinity purified polyclonal antibody (Catalog # A14534-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IAH1 at approximately 28 kDa. The expected band size for IAH1 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14534-1-iah1-primary-antibodies-ihc-testing-3.jpgAnti-IAH1 Antibody Picoband®IHC analysis of IAH1 using anti-IAH1 antibody (A14534-1). IAH1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IAH1 Antibody (A14534-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14534-1-iah1-primary-antibodies-ihc-testing-2.jpgAnti-IAH1 Antibody Picoband® IHC analysis of IAH1 using anti-IAH1 antibody (A14534-1). IAH1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IAH1 Antibody (A14534-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14534-1-iah1-primary-antibodies-if-testing-3.jpgAnti-IAH1 Antibody Picoband® IF analysis of IAH1 using anti-IAH1 antibody (A14534-1). IAH1 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IAH1 Antibody (A14534-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14534-1-iah1-primary-antibodies-fcm-testing-4.pngAnti-IAH1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-IAH1 antibody (A14534-1). Overlay histogram showing A549 cells stained with A14534-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IAH1 Antibody (A14534-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-iars1-picoband-trade-antibody-a06805-1-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06805-1-iars-primary-antibodies-wb-testing-1.jpgAnti-IARS1 Antibody Picoband® Western blot analysis of IARS1 using anti-IARS1 antibody (A06805-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IARS1 antigen affinity purified polyclonal antibody (Catalog # A06805-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IARS1 at approximately 144 kDa. The expected band size for IARS1 is at 144 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06805-1-iars-primary-antibodies-ihc-testing-2.jpgAnti-IARS1 Antibody Picoband® IHC analysis of IARS1 using anti-IARS1 antibody (A06805-1). IARS1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS1 Antibody (A06805-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06805-1-iars-primary-antibodies-ihc-testing-3.jpgAnti-IARS1 Antibody Picoband® IHC analysis of IARS1 using anti-IARS1 antibody (A06805-1). IARS1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS1 Antibody (A06805-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06805-1-iars-primary-antibodies-ihc-testing-4.jpgAnti-IARS1 Antibody Picoband® IHC analysis of IARS1 using anti-IARS1 antibody (A06805-1). IARS1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS1 Antibody (A06805-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06805-1-iars-primary-antibodies-fcm-testing-5.pngAnti-IARS1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-IARS1 antibody (A06805-1). Overlay histogram showing HepG2 cells stained with A06805-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IARS1 Antibody (A06805-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-iars2-picoband-trade-antibody-a09580-2-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09580-2-iars2-primary-antibodies-wb-testing-1.jpgAnti-IARS2 Antibody Picoband® Western blot analysis of IARS2 using anti-IARS2 antibody (A09580-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: human Hacat whole cell lysates, Lane 6: human HepG2 whole cell lysates, Lane 7: rat brain tissue lysates, Lane 8: rat kidney tissue lysates, Lane 9: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IARS2 antigen affinity purified polyclonal antibody (Catalog # A09580-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IARS2 at approximately 114 kDa. The expected band size for IARS2 is at 114 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09580-2-iars2-primary-antibodies-ihc-testing-2.jpgAnti-IARS2 Antibody Picoband® IHC analysis of IARS2 using anti-IARS2 antibody (A09580-2). IARS2 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS2 Antibody (A09580-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09580-2-iars2-primary-antibodies-ihc-testing-3.jpgAnti-IARS2 Antibody Picoband® IHC analysis of IARS2 using anti-IARS2 antibody (A09580-2). IARS2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS2 Antibody (A09580-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09580-2-iars2-primary-antibodies-ihc-testing-4.jpgAnti-IARS2 Antibody Picoband® IHC analysis of IARS2 using anti-IARS2 antibody (A09580-2). IARS2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS2 Antibody (A09580-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09580-2-iars2-primary-antibodies-ihc-testing-5.jpgAnti-IARS2 Antibody Picoband® IHC analysis of IARS2 using anti-IARS2 antibody (A09580-2). IARS2 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS2 Antibody (A09580-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09580-2-iars2-primary-antibodies-ihc-testing-6.jpgAnti-IARS2 Antibody Picoband® IHC analysis of IARS2 using anti-IARS2 antibody (A09580-2). IARS2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IARS2 Antibody (A09580-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09580-2-iars2-primary-antibodies-fcm-testing-7.pngAnti-IARS2 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-IARS2 antibody (A09580-2). Overlay histogram showing 293T cells stained with A09580-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IARS2 Antibody (A09580-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-icam5-picoband-trade-antibody-a07187-2-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07187-2-icam5-primary-antibodies-wb-testing-1.jpgAnti-ICAM5 Antibody Picoband® Western blot analysis of ICAM5 using anti-ICAM5 antibody (A07187-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICAM5 antigen affinity purified polyclonal antibody (Catalog # A07187-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ICAM5 at approximately 140 kDa. The expected band size for ICAM5 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07187-2-icam5-primary-antibodies-fcm-testing-2.pngAnti-ICAM5 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-ICAM5 antibody (A07187-2). Overlay histogram showing Hela cells stained with A07187-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ICAM5 Antibody (A07187-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-idh3a-picoband-trade-antibody-a09544-3-boster.html2026-03-16T09:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-wb-testing-1.jpgAnti-IDH3A Antibody Picoband® Western blot analysis of ILDR1 using anti-ILDR1 antibody (A09544-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat heart tissue lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ILDR1 antigen affinity purified polyclonal antibody (Catalog # A09544-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ILDR1 at approximately 37 kDa. The expected band size for ILDR1 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-ihc-testing-2.jpgAnti-IDH3A Antibody Picoband® IHC analysis of ILDR1 using anti-ILDR1 antibody (A09544-3). ILDR1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ILDR1 Antibody (A09544-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-ihc-testing-3.jpgAnti-IDH3A Antibody Picoband® IHC analysis of ILDR1 using anti-ILDR1 antibody (A09544-3). ILDR1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ILDR1 Antibody (A09544-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-ihc-testing-4.jpgAnti-IDH3A Antibody Picoband® IHC analysis of ILDR1 using anti-ILDR1 antibody (A09544-3). ILDR1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ILDR1 Antibody (A09544-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-if-testing-5.jpgAnti-IDH3A Antibody Picoband® IF analysis of ILDR1 using anti-ILDR1 antibody (A09544-3). ILDR1 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ILDR1 Antibody (A09544-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-if-testing-6.jpgAnti-IDH3A Antibody Picoband® IF analysis of ILDR1 using anti-ILDR1 antibody (A09544-3). ILDR1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ILDR1 Antibody (A09544-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-if-testing-7.jpgAnti-IDH3A Antibody Picoband® IF analysis of ILDR1 using anti-ILDR1 antibody (A09544-3). ILDR1 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ILDR1 Antibody (A09544-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09544-3-idh3a-primary-antibodies-fcm-testing-8.pngAnti-IDH3A Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ILDR1 antibody (A09544-3). Overlay histogram showing HepG2 cells stained with A09544-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ILDR1 Antibody (A09544-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-idh3g-picoband-trade-antibody-a10370-3-boster.html2026-03-16T09:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-wb-testing-1_1.jpgAnti-IDH3G Antibody Picoband® Western blot analysis of IDH3G using anti-IDH3G antibody (A10370-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: human U251 whole cell lysates, Lane 6: monkey COS-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDH3G antigen affinity purified polyclonal antibody (Catalog # A10370-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDH3G at approximately 40 kDa. The expected band size for IDH3G is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-wb-testing-2_1.jpgAnti-IDH3G Antibody Picoband® Western blot analysis of IDH3G using anti-IDH3G antibody (A10370-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse kidney tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: rat HBZY whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDH3G antigen affinity purified polyclonal antibody (Catalog # A10370-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDH3G at approximately 40 kDa. The expected band size for IDH3G is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-ihc-testing-3.jpgAnti-IDH3G Antibody Picoband® IHC analysis of IDH3G using anti-IDH3G antibody (A10370-3). IDH3G was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3G Antibody (A10370-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-ihc-testing-4.jpgAnti-IDH3G Antibody Picoband® IHC analysis of IDH3G using anti-IDH3G antibody (A10370-3). IDH3G was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3G Antibody (A10370-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-ihc-testing-5.jpgAnti-IDH3G Antibody Picoband® IHC analysis of IDH3G using anti-IDH3G antibody (A10370-3). IDH3G was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3G Antibody (A10370-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-ihc-testing-6.jpgAnti-IDH3G Antibody Picoband® IHC analysis of IDH3G using anti-IDH3G antibody (A10370-3). IDH3G was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3G Antibody (A10370-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-ihc-testing-7.jpgAnti-IDH3G Antibody Picoband® IHC analysis of IDH3G using anti-IDH3G antibody (A10370-3). IDH3G was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3G Antibody (A10370-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-if-testing-8.jpgAnti-IDH3G Antibody Picoband® IF analysis of IDH3G using anti-IDH3G antibody (A10370-3). IDH3G was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IDH3G Antibody (A10370-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10370-3-idh3g-primary-antibodies-fcm-testing-9.pngAnti-IDH3G Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-IDH3G antibody (A10370-3). Overlay histogram showing 293T cells stained with A10370-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IDH3G Antibody (A10370-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-idi1-picoband-trade-antibody-a07892-1-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07892-1-idi1-primary-antibodies-wb-testing-1.jpgAnti-IDI1 Antibody Picoband® Western blot analysis of IDI1 using anti-IDI1 antibody (A07892-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDI1 antigen affinity purified polyclonal antibody (Catalog # A07892-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDI1 at approximately 26-28 kDa. The expected band size for IDI1 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07892-1-fnut-12-1584551-g008.jpgAnti-IDI1 Antibody Picoband®Expression analyses of transcription or protein levels of selected genes. (A) Expression analyses of selected genes by qRT–PCR. The data represent the means ± SDs from six biological replicates with three technical replicates. (B–D) FCJ/RCJ upregulated ABCC3, IDI1, and APOA2 expression in the liver. FCJ and RCJ significantly upregulated hepatic ABCC3 (B) and IDI1 (C) expression, and RCJ significantly upregulated hepatic APOA2 (D) expression in T2DM rats. The data represent the means ± SDs from three biological replicates with three technical replicates. * p < 0.05, *** p < 0.001, **** p < 0.0001. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/nutrition/articles/10.3389/fnut.2025.1584551/full'>40458826</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07892-1-idi1-primary-antibodies-ihc-testing-2.jpgAnti-IDI1 Antibody Picoband® IHC analysis of IDI1 using anti-IDI1 antibody (A07892-1). IDI1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDI1 Antibody (A07892-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07892-1-idi1-primary-antibodies-ihc-testing-3.jpgAnti-IDI1 Antibody Picoband® IHC analysis of IDI1 using anti-IDI1 antibody (A07892-1). IDI1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDI1 Antibody (A07892-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07892-1-idi1-primary-antibodies-ihc-testing-4.jpgAnti-IDI1 Antibody Picoband® IHC analysis of IDI1 using anti-IDI1 antibody (A07892-1). IDI1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDI1 Antibody (A07892-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07892-1-idi1-primary-antibodies-fcm-testing-5.pngAnti-IDI1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-IDI1 antibody (A07892-1). Overlay histogram showing 293T cells stained with A07892-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IDI1 Antibody (A07892-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-idi2-picoband-trade-antibody-a11225-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11225-idi2-primary-antibodies-wb-testing-1.jpgAnti-IDI2 Antibody Picoband® Western blot analysis of IDI2 using anti-IDI2 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDI2 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDI2 at approximately 27 kDa. The expected band size for IDI2 is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11225-idi2-primary-antibodies-fcm-testing-2.pngAnti-IDI2 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-IDI2 antibody (A11225). Overlay histogram showing Caco-2 cells stained with A11225 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IDI2 Antibody (A11225, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-idua-picoband-trade-antibody-a02281-2-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-wb-testing-1.jpgAnti-IDUA Antibody Picoband® Western blot analysis of IDUA using anti-IDUA antibody (A02281-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human U87 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDUA antigen affinity purified polyclonal antibody (Catalog # A02281-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDUA at approximately 73 kDa. The expected band size for IDUA is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-ihc-testing-2.jpgAnti-IDUA Antibody Picoband® IHC analysis of IDUA using anti-IDUA antibody (A02281-2). IDUA was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDUA Antibody (A02281-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-ihc-testing-3.jpgAnti-IDUA Antibody Picoband® IHC analysis of IDUA using anti-IDUA antibody (A02281-2). IDUA was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDUA Antibody (A02281-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-ihc-testing-4.jpgAnti-IDUA Antibody Picoband® IHC analysis of IDUA using anti-IDUA antibody (A02281-2). IDUA was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDUA Antibody (A02281-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-ihc-testing-5.jpgAnti-IDUA Antibody Picoband® IHC analysis of IDUA using anti-IDUA antibody (A02281-2). IDUA was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDUA Antibody (A02281-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-ihc-testing-6.jpgAnti-IDUA Antibody Picoband® IHC analysis of IDUA using anti-IDUA antibody (A02281-2). IDUA was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDUA Antibody (A02281-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-if-testing-7.jpgAnti-IDUA Antibody Picoband® IF analysis of IDUA using anti-IDUA antibody (A02281-2). IDUA was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-IDUA Antibody (A02281-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02281-2-idua-primary-antibodies-fcm-testing-8.pngAnti-IDUA Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-IDUA antibody (A02281-2). Overlay histogram showing SH-SY5Y cells stained with A02281-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IDUA Antibody (A02281-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-iffo1-picoband-trade-antibody-a17273-1-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17273-1-iffo1-primary-antibodies-wb-testing-1.jpgAnti-IFFO1 Antibody Picoband® Western blot analysis of IFFO1 using anti-IFFO1 antibody (A17273-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFFO1 antigen affinity purified polyclonal antibody (Catalog # A17273-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFFO1 at approximately 30 kDa. The expected band size for IFFO1 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17273-1-iffo1-primary-antibodies-ihc-testing-2.jpgAnti-IFFO1 Antibody Picoband® IHC analysis of IFFO1 using anti-IFFO1 antibody (A17273-1). IFFO1 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFFO1 Antibody (A17273-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17273-1-iffo1-primary-antibodies-ihc-testing-3.jpgAnti-IFFO1 Antibody Picoband® IHC analysis of IFFO1 using anti-IFFO1 antibody (A17273-1). IFFO1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFFO1 Antibody (A17273-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17273-1-iffo1-primary-antibodies-if-testing-4.jpgAnti-IFFO1 Antibody Picoband® IF analysis of IFFO1 using anti-IFFO1 antibody (A17273-1) and anti-Beta Tubulin antibody (M01857-3). IFFO1 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IFFO1 Antibody (A17273-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17273-1-iffo1-primary-antibodies-fcm-testing-5.pngAnti-IFFO1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-IFFO1 antibody (A17273-1). Overlay histogram showing SH-SY5Y cells stained with A17273-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFFO1 Antibody (A17273-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ifngr1-picoband-trade-antibody-a01716-4-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01716-4-ifngr1-primary-antibodies-wb-testing-1.jpgAnti-Ifngr1 Antibody Picoband® Western blot analysis of Ifngr1 using anti-Ifngr1 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat thymus tissue lysates, Lane 2: mouse thymus tissue lysates, Lane 3: mouse spleen tissue lysates, Lane 4: mouse lung tissue lysates, Lane 5: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Ifngr1 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Ifngr1 at approximately 96 kDa. The expected band size for Ifngr1 is at 52 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-ift52-picoband-trade-antibody-a12872-1-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12872-1-ift52-primary-antibodies-wb-testing-1.jpgAnti-IFT52 Antibody Picoband® Western blot analysis of IFT52 using anti-IFT52 antibody (A12872-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFT52 antigen affinity purified polyclonal antibody (Catalog # A12872-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFT52 at approximately 45 kDa. The expected band size for IFT52 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12872-1-ift52-primary-antibodies-ihc-testing-2.jpgAnti-IFT52 Antibody Picoband® IHC analysis of IFT52 using anti-IFT52 antibody (A12872-1). IFT52 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT52 Antibody (A12872-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12872-1-ift52-primary-antibodies-ihc-testing-3.jpgAnti-IFT52 Antibody Picoband® IHC analysis of IFT52 using anti-IFT52 antibody (A12872-1). IFT52 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT52 Antibody (A12872-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12872-1-ift52-primary-antibodies-ihc-testing-4.jpgAnti-IFT52 Antibody Picoband® IHC analysis of IFT52 using anti-IFT52 antibody (A12872-1). IFT52 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT52 Antibody (A12872-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12872-1-ift52-primary-antibodies-ihc-testing-5.jpgAnti-IFT52 Antibody Picoband® IHC analysis of IFT52 using anti-IFT52 antibody (A12872-1). IFT52 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT52 Antibody (A12872-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12872-1-ift52-primary-antibodies-if-testing-6.jpgAnti-IFT52 Antibody Picoband® IF analysis of IFT52 using anti-IFT52 antibody (A12872-1). IFT52 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-IFT52 Antibody (A12872-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12872-1-ift52-primary-antibodies-fcm-testing-7.pngAnti-IFT52 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-IFT52 antibody (A12872-1). Overlay histogram showing HepG2 cells stained with A12872-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-IFT52 Antibody (A12872-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-cd316-igsf8-picoband-trade-antibody-a06844-2-boster.html2026-03-16T09:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06844-2-igsf8-primary-antibodies-wb-testing-1.jpgAnti-CD316/IGSF8 Antibody Picoband® Western blot analysis of CD316/IGSF8 using anti-CD316/IGSF8 antibody (A06844-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: human HepG2 whole cell lysates, Lane 6: rat brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD316/IGSF8 antigen affinity purified polyclonal antibody (Catalog # A06844-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD316/IGSF8 at approximately 70 kDa. The expected band size for CD316/IGSF8 is at 65 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-ikzf3-picoband-trade-antibody-a01611-2-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01611-2-ikzf3-primary-antibodies-wb-testing-1.jpgAnti-IKZF3 Antibody Picoband® Western blot analysis of IKZF3 using anti-IKZF3 antibody (A01611-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human Ramos whole cell lysates, Lane 3: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IKZF3 antigen affinity purified polyclonal antibody (Catalog # A01611-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IKZF3 at approximately 70 kDa. The expected band size for IKZF3 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01611-2-ikzf3-primary-antibodies-ihc-testing-2.jpgAnti-IKZF3 Antibody Picoband® IHC analysis of IKZF3 using anti-IKZF3 antibody (A01611-2). IKZF3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IKZF3 Antibody (A01611-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01611-2-ikzf3-primary-antibodies-ihc-testing-3.jpgAnti-IKZF3 Antibody Picoband® IHC analysis of IKZF3 using anti-IKZF3 antibody (A01611-2). IKZF3 was detected in a paraffin-embedded section of rat thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IKZF3 Antibody (A01611-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01611-2-ikzf3-primary-antibodies-ihc-testing-4.jpgAnti-IKZF3 Antibody Picoband® IHC analysis of IKZF3 using anti-IKZF3 antibody (A01611-2). IKZF3 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IKZF3 Antibody (A01611-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01611-2-ikzf3-primary-antibodies-if-testing-5.jpgAnti-IKZF3 Antibody Picoband® IF analysis of IKZF3 using anti-IKZF3 antibody (A01611-2) and anti-Beta Tubulin antibody (M01857-3). IKZF3 was detected in immunocytochemical section of SIHA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IKZF3 Antibody (A01611-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01611-2-ikzf3-primary-antibodies-fcm-testing-6.pngAnti-IKZF3 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-IKZF3 antibody (A01611-2). Overlay histogram showing THP-1 cells stained with A01611-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IKZF3 Antibody (A01611-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ildr1-picoband-trade-antibody-a09114-1-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09114-1-ildr1-primary-antibodies-wb-testing-1.jpgAnti-ILDR1 Antibody Picoband® Western blot analysis of ILDR1 using anti-ILDR1 antibody (A09114-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ILDR1 antigen affinity purified polyclonal antibody (Catalog # A09114-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ILDR1 at approximately 63 kDa. The expected band size for ILDR1 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09114-1-ildr1-primary-antibodies-fcm-testing-2.pngAnti-ILDR1 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-ILDR1 antibody (A09114-1). Overlay histogram showing PC-3 cells stained with A09114-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ILDR1 Antibody (A09114-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nf45-ilf2-picoband-trade-antibody-a04443-2-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-wb-testing-1.jpgAnti-NF45/ILF2 Antibody Picoband® Western blot analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NF45/ILF2 antigen affinity purified polyclonal antibody (Catalog # A04443-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NF45/ILF2 at approximately 43 kDa. The expected band size for NF45/ILF2 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-ihc-testing-2.jpgAnti-NF45/ILF2 Antibody Picoband® IHC analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). NF45/ILF2 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NF45/ILF2 Antibody (A04443-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-ihc-testing-3.jpgAnti-NF45/ILF2 Antibody Picoband® IHC analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). NF45/ILF2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NF45/ILF2 Antibody (A04443-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-ihc-testing-4.jpgAnti-NF45/ILF2 Antibody Picoband® IHC analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). NF45/ILF2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NF45/ILF2 Antibody (A04443-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-ihc-testing-5.jpgAnti-NF45/ILF2 Antibody Picoband® IHC analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). NF45/ILF2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NF45/ILF2 Antibody (A04443-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-ihc-testing-6.jpgAnti-NF45/ILF2 Antibody Picoband® IHC analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). NF45/ILF2 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NF45/ILF2 Antibody (A04443-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-ihc-testing-7.jpgAnti-NF45/ILF2 Antibody Picoband® IHC analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). NF45/ILF2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NF45/ILF2 Antibody (A04443-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-ihc-testing-8.jpgAnti-NF45/ILF2 Antibody Picoband® IHC analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2). NF45/ILF2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NF45/ILF2 Antibody (A04443-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-if-testing-9.jpgAnti-NF45/ILF2 Antibody Picoband® IF analysis of NF45/ILF2 using anti-NF45/ILF2 antibody (A04443-2) and anti-Beta Tubulin antibody (M01857-3). NF45/ILF2 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NF45/ILF2 Antibody (A04443-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04443-2-ilf2-primary-antibodies-fcm-testing-10.pngAnti-NF45/ILF2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-NF45/ILF2 antibody (A04443-2). Overlay histogram showing JK cells stained with A04443-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NF45/ILF2 Antibody (A04443-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ilkap-picoband-trade-antibody-a08074-1-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08074-1-ilkap-primary-antibodies-wb-testing-1.jpgAnti-ILKAP Antibody Picoband® Western blot analysis of ILKAP using anti-ILKAP antibody (A08074-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ILKAP antigen affinity purified polyclonal antibody (Catalog # A08074-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ILKAP at approximately 43 kDa. The expected band size for ILKAP is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08074-1-ilkap-primary-antibodies-if-testing-2.jpgAnti-ILKAP Antibody Picoband® IF analysis of ILKAP using anti-ILKAP antibody (A08074-1) and anti-Beta Tubulin antibody (M01857-3). ILKAP was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ILKAP Antibody (A08074-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08074-1-ilkap-primary-antibodies-fcm-testing-3.pngAnti-ILKAP Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ILKAP antibody (A08074-1). Overlay histogram showing HepG2 cells stained with A08074-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ILKAP Antibody (A08074-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mitofilin-immt-picoband-trade-antibody-a04102-2-boster.html2026-03-16T09:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-wb-testing-1.jpgAnti-Mitofilin/IMMT Antibody Picoband® Western blot analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Colo320 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat NRK whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse HEPA1/6 whole cell lysates, Lane 7: mouse MFC whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Mitofilin/IMMT antigen affinity purified polyclonal antibody (Catalog # A04102-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Mitofilin/IMMT at approximately 80-90 kDa. The expected band size for Mitofilin/IMMT is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-ihc-testing-2.jpgAnti-Mitofilin/IMMT Antibody Picoband® IHC analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Mitofilin/IMMT was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Mitofilin/IMMT Antibody (A04102-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-ihc-testing-3.jpgAnti-Mitofilin/IMMT Antibody Picoband® IHC analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Mitofilin/IMMT was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Mitofilin/IMMT Antibody (A04102-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-ihc-testing-4.jpgAnti-Mitofilin/IMMT Antibody Picoband® IHC analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Mitofilin/IMMT was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Mitofilin/IMMT Antibody (A04102-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-ihc-testing-5.jpgAnti-Mitofilin/IMMT Antibody Picoband® IHC analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Mitofilin/IMMT was detected in a paraffin-embedded section of human testicular germ cell tumors tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Mitofilin/IMMT Antibody (A04102-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-ihc-testing-6.jpgAnti-Mitofilin/IMMT Antibody Picoband® IHC analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Mitofilin/IMMT was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Mitofilin/IMMT Antibody (A04102-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-ihc-testing-7.jpgAnti-Mitofilin/IMMT Antibody Picoband® IHC analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Mitofilin/IMMT was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Mitofilin/IMMT Antibody (A04102-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-if-testing-8.jpgAnti-Mitofilin/IMMT Antibody Picoband® IF analysis of Mitofilin/IMMT using anti-Mitofilin/IMMT antibody (A04102-2). Mitofilin/IMMT was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Mitofilin/IMMT Antibody (A04102-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04102-2-immt-primary-antibodies-fcm-testing-9.pngAnti-Mitofilin/IMMT Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Mitofilin/IMMT antibody (A04102-2). Overlay histogram showing HepG2 cells stained with A04102-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Mitofilin/IMMT Antibody (A04102-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-bcl3-picoband-trade-antibody-a02773-4-boster.html2026-03-17T05:15:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02773-4-bcl3-primary-antibodies-wb-testing-1.jpgAnti-BCL3 Antibody Picoband® Western blot analysis of BCL3 using anti-BCL3 antibody (A02773-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates, Lane 2: human hepatocellular carcinoma tumor tissue (HCCT) lysates, Lane 3: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCL3 antigen affinity purified polyclonal antibody (Catalog # A02773-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCL3 at approximately 60 kDa. The expected band size for BCL3 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02773-4-bcl3-primary-antibodies-if-testing-2.jpgAnti-BCL3 Antibody Picoband® IF analysis of BCL3 using anti-BCL3 antibody (A02773-4) and anti-Beta Tubulin antibody (M01857-3). BCL3 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BCL3 Antibody (A02773-4) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02773-4-bcl3-primary-antibodies-fcm-testing-3.pngAnti-BCL3 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-BCL3 antibody (A02773-4). Overlay histogram showing PC-3 cells stained with A02773-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BCL3 Antibody (A02773-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ift74-picoband-trade-antibody-a08931-2-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08931-2-ift74-primary-antibodies-wb-testing-1.jpgAnti-IFT74 Antibody Picoband® Western blot analysis of IFT74 using anti-IFT74 antibody (A08931-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFT74 antigen affinity purified polyclonal antibody (Catalog # A08931-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFT74 at approximately 69 kDa. The expected band size for IFT74 is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08931-2-ift74-primary-antibodies-ihc-testing-2.jpgAnti-IFT74 Antibody Picoband® IHC analysis of IFT74 using anti-IFT74 antibody (A08931-2). IFT74 was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT74 Antibody (A08931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08931-2-ift74-primary-antibodies-ihc-testing-3.jpgAnti-IFT74 Antibody Picoband® IHC analysis of IFT74 using anti-IFT74 antibody (A08931-2). IFT74 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT74 Antibody (A08931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08931-2-ift74-primary-antibodies-ihc-testing-4.jpgAnti-IFT74 Antibody Picoband® IHC analysis of IFT74 using anti-IFT74 antibody (A08931-2). IFT74 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT74 Antibody (A08931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08931-2-ift74-primary-antibodies-ihc-testing-5.jpgAnti-IFT74 Antibody Picoband® IHC analysis of IFT74 using anti-IFT74 antibody (A08931-2). IFT74 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT74 Antibody (A08931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08931-2-ift74-primary-antibodies-ihc-testing-6.jpgAnti-IFT74 Antibody Picoband® IHC analysis of IFT74 using anti-IFT74 antibody (A08931-2). IFT74 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFT74 Antibody (A08931-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08931-2-ift74-primary-antibodies-fcm-testing-7.pngAnti-IFT74 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-IFT74 antibody (A08931-2). Overlay histogram showing JK cells stained with A08931-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-IFT74 Antibody (A08931-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-imp4-picoband-trade-antibody-a10469-1-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10469-1-imp4-primary-antibodies-wb-testing-1.jpgAnti-IMP4 Antibody Picoband® Western blot analysis of IMP4 using anti-IMP4 antibody (A10469-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: mouse thymus tissue lysates, Lane 5: mouse RAW264.7 whole cell lysates, Lane 6: mouse EL-4 whole cell lysates, Lane 7: mouse Ana-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IMP4 antigen affinity purified polyclonal antibody (Catalog # A10469-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IMP4 at approximately 36 kDa. The expected band size for IMP4 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10469-1-imp4-primary-antibodies-if-testing-2.jpgAnti-IMP4 Antibody Picoband® IF analysis of IMP4 using anti-IMP4 antibody (A10469-1) and anti-Beta Tubulin antibody (M01857-3). IMP4 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IMP4 Antibody (A10469-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10469-1-imp4-primary-antibodies-fcm-testing-3.pngAnti-IMP4 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-IMP4 antibody (A10469-1). Overlay histogram showing HepG2 cells stained with A10469-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IMP4 Antibody (A10469-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-impg2-picoband-trade-antibody-a10288-1-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10288-1-impg2-primary-antibodies-wb-testing-1.jpgAnti-IMPG2 Antibody Picoband® Western blot analysis of IMPG2 using anti-IMPG2 antibody (A10288-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IMPG2 antigen affinity purified polyclonal antibody (Catalog # A10288-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IMPG2 at approximately 150 kDa. The expected band size for IMPG2 is at 139 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10288-1-impg2-primary-antibodies-ihc-testing-2.jpgAnti-IMPG2 Antibody Picoband® IHC analysis of IMPG2 using anti-IMPG2 antibody (A10288-1). IMPG2 was detected in a paraffin-embedded section of rat retina tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IMPG2 Antibody (A10288-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-cd14-picoband-trade-antibody-a00137-3-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00137-3-cd14-primary-antibodies-wb-testing-1.jpgAnti-Cd14 Antibody Picoband® Western blot analysis of Cd14 using anti-Cd14 antibody (A00137-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cd14 antigen affinity purified polyclonal antibody (Catalog # A00137-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cd14 at approximately 50 kDa. The expected band size for Cd14 is at 39 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-mapk13-picoband-trade-antibody-a03594-boster.html2026-03-17T05:13:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03594-mapk13-primary-antibodies-wb-testing-1.jpgAnti-MAPK13 Antibody Picoband® Western blot analysis of MAPK13 using anti-MAPK13 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human T-47D whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAPK13 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAPK13 at approximately 42 kDa. The expected band size for MAPK13 is at 42 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-rtca-picoband-trade-antibody-a07570-2-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07570-2-rtca-primary-antibodies-wb-testing-1.jpgAnti-RTCA Antibody Picoband® Western blot analysis of RTCA using anti-RTCA antibody (A07570-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RTCA antigen affinity purified polyclonal antibody (Catalog # A07570-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RTCA at approximately 39 kDa. The expected band size for RTCA is at 39 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-pard6b-picoband-trade-antibody-a08475-2-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08475-2-pard6b-primary-antibodies-wb-testing-1.jpgAnti-PARD6B Antibody Picoband® Western blot analysis of PARD6B using anti-PARD6B antibody (A08475-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARD6B antigen affinity purified polyclonal antibody (Catalog # A08475-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARD6B at approximately 50 kDa. The expected band size for PARD6B is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08475-2-pard6b-primary-antibodies-ihc-testing-4.jpgAnti-PARD6B Antibody Picoband®IHC analysis of PARD6B using anti-PARD6B antibody (A08475-2). PARD6B was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PARD6B Antibody (A08475-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08475-2-pard6b-primary-antibodies-ihc-testing-2.jpgAnti-PARD6B Antibody Picoband® IHC analysis of PARD6B using anti-PARD6B antibody (A08475-2). PARD6B was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PARD6B Antibody (A08475-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08475-2-pard6b-primary-antibodies-ihc-testing-3.jpgAnti-PARD6B Antibody Picoband® IHC analysis of PARD6B using anti-PARD6B antibody (A08475-2). PARD6B was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PARD6B Antibody (A08475-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08475-2-pard6b-primary-antibodies-if-testing-4.jpgAnti-PARD6B Antibody Picoband® IF analysis of PARD6B using anti-PARD6B antibody (A08475-2). PARD6B was detected in an immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PARD6B Antibody (A08475-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08475-2-pard6b-primary-antibodies-fcm-testing-5.pngAnti-PARD6B Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PARD6B antibody (A08475-2). Overlay histogram showing MCF-7 cells stained with A08475-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PARD6B Antibody (A08475-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pawr-picoband-trade-antibody-a03637-2-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03637-2-pawr-primary-antibodies-wb-testing-1.jpgAnti-PAWR Antibody Picoband® Western blot analysis of PAWR using anti-PAWR antibody (A03637-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SW620 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAWR antigen affinity purified polyclonal antibody (Catalog # A03637-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAWR at approximately 41 kDa. The expected band size for PAWR is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03637-2-pawr-primary-antibodies-if-testing-2.jpgAnti-PAWR Antibody Picoband® IF analysis of PAWR using anti-PAWR antibody (A03637-2). PAWR was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PAWR Antibody (A03637-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03637-2-pawr-primary-antibodies-fcm-testing-3.pngAnti-PAWR Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-PAWR antibody (A03637-2). Overlay histogram showing Caco-2 cells stained with A03637-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PAWR Antibody (A03637-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-otub1-picoband-trade-antibody-a04361-1-boster.html2026-03-16T09:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04361-1-otub1-primary-antibodies-wb-testing-1.jpgAnti-OTUB1 Antibody Picoband® Western blot analysis of OTUB1 using anti-OTUB1 antibody (A04361-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OTUB1 antigen affinity purified polyclonal antibody (Catalog # A04361-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OTUB1 at approximately 36 kDa. The expected band size for OTUB1 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04361-1-otub1-primary-antibodies-ihc-testing-2.jpgAnti-OTUB1 Antibody Picoband® IHC analysis of OTUB1 using anti-OTUB1 antibody (A04361-1). OTUB1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OTUB1 Antibody (A04361-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04361-1-otub1-primary-antibodies-ihc-testing-3.jpgAnti-OTUB1 Antibody Picoband® IHC analysis of OTUB1 using anti-OTUB1 antibody (A04361-1). OTUB1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OTUB1 Antibody (A04361-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04361-1-otub1-primary-antibodies-ihc-testing-4.jpgAnti-OTUB1 Antibody Picoband® IHC analysis of OTUB1 using anti-OTUB1 antibody (A04361-1). OTUB1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OTUB1 Antibody (A04361-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04361-1-otub1-primary-antibodies-ihc-testing-5.jpgAnti-OTUB1 Antibody Picoband® IHC analysis of OTUB1 using anti-OTUB1 antibody (A04361-1). OTUB1 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OTUB1 Antibody (A04361-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04361-1-otub1-primary-antibodies-fcm-testing-6.pngAnti-OTUB1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-OTUB1 antibody (A04361-1). Overlay histogram showing MCF-7 cells stained with A04361-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-OTUB1 Antibody (A04361-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-paaf1-picoband-trade-antibody-a12843-1-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12843-1-paaf1-primary-antibodies-wb-testing-1.jpgAnti-PAAF1 Antibody Picoband® Western blot analysis of PAAF1 using anti-PAAF1 antibody (A12843-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAAF1 antigen affinity purified polyclonal antibody (Catalog # A12843-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAAF1 at approximately 42 kDa. The expected band size for PAAF1 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12843-1-paaf1-primary-antibodies-if-testing-2.jpgAnti-PAAF1 Antibody Picoband® IF analysis of PAAF1 using anti-PAAF1 antibody (A12843-1) and anti-Beta Tubulin antibody (M01857-3). PAAF1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PAAF1 Antibody (A12843-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12843-1-paaf1-primary-antibodies-fcm-testing-3.pngAnti-PAAF1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PAAF1 antibody (A12843-1). Overlay histogram showing JK cells stained with A12843-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PAAF1 Antibody (A12843-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-paics-picoband-trade-antibody-a07031-1-boster.html2026-03-16T09:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07031-1-paics-primary-antibodies-wb-testing-1.jpgAnti-PAICS Antibody Picoband® Western blot analysis of PAICS using anti-PAICS antibody (A07031-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Raji whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAICS antigen affinity purified polyclonal antibody (Catalog # A07031-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAICS at approximately 47 kDa. The expected band size for PAICS is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07031-1-paics-primary-antibodies-fcm-testing-2.pngAnti-PAICS Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-PAICS antibody (A07031-1). Overlay histogram showing PC-3 cells stained with A07031-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PAICS Antibody (A07031-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-paip1-picoband-trade-antibody-a07792-2-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07792-2-paip1-primary-antibodies-wb-testing-1.jpgAnti-PAIP1 Antibody Picoband® Western blot analysis of PAIP1 using anti-PAIP1 antibody (A07792-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAIP1 antigen affinity purified polyclonal antibody (Catalog # A07792-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAIP1 at approximately 45 kDa. The expected band size for PAIP1 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07792-2-paip1-primary-antibodies-ihc-testing-2.jpgAnti-PAIP1 Antibody Picoband® IHC analysis of PAIP1 using anti-PAIP1 antibody (A07792-2). PAIP1 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAIP1 Antibody (A07792-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07792-2-paip1-primary-antibodies-ihc-testing-3.jpgAnti-PAIP1 Antibody Picoband® IHC analysis of PAIP1 using anti-PAIP1 antibody (A07792-2). PAIP1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAIP1 Antibody (A07792-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07792-2-paip1-primary-antibodies-if-testing-4.jpgAnti-PAIP1 Antibody Picoband® IF analysis of PAIP1 using anti-PAIP1 antibody (A07792-2). PAIP1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PAIP1 Antibody (A07792-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07792-2-paip1-primary-antibodies-fcm-testing-5.pngAnti-PAIP1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PAIP1 antibody (A07792-2). Overlay histogram showing SH-SY5Y cells stained with A07792-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PAIP1 Antibody (A07792-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-atg7-picoband-trade-antibody-a00346-5-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-wb-testing-1.jpgAnti-ATG7 Antibody Picoband® Western blot analysis of ATG7 using anti-ATG7 antibody (A00346-5). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATG7 antigen affinity purified polyclonal antibody (Catalog # A00346-5) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATG7 at approximately 78 kDa. The expected band size for ATG7 is at 78 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-ihc-testing-2.jpgAnti-ATG7 Antibody Picoband® IHC analysis of ATG7 using anti-ATG7 antibody (A00346-5). ATG7 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATG7 Antibody (A00346-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-ihc-testing-3.jpgAnti-ATG7 Antibody Picoband® IHC analysis of ATG7 using anti-ATG7 antibody (A00346-5). ATG7 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATG7 Antibody (A00346-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-ihc-testing-4.jpgAnti-ATG7 Antibody Picoband® IHC analysis of ATG7 using anti-ATG7 antibody (A00346-5). ATG7 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATG7 Antibody (A00346-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-ihc-testing-5.jpgAnti-ATG7 Antibody Picoband® IHC analysis of ATG7 using anti-ATG7 antibody (A00346-5). ATG7 was detected in a paraffin-embedded section of human meningioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATG7 Antibody (A00346-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-ihc-testing-6.jpgAnti-ATG7 Antibody Picoband® IHC analysis of ATG7 using anti-ATG7 antibody (A00346-5). ATG7 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATG7 Antibody (A00346-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-if-testing-7.jpgAnti-ATG7 Antibody Picoband® IF analysis of ATG7 using anti-ATG7 antibody (A00346-5). ATG7 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ATG7 Antibody (A00346-5) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00346-5-atg7-primary-antibodies-fcm-testing-8.pngAnti-ATG7 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ATG7 antibody (A00346-5). Overlay histogram showing HepG2 cells stained with A00346-5 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ATG7 Antibody (A00346-5, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ing2-picoband-trade-antibody-a04290-3-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04290-3-ing2-primary-antibodies-wb-testing-1.jpgAnti-ING2 Antibody Picoband® Western blot analysis of ING2 using anti-ING2 antibody (A04290-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat thymus tissue lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse thymus tissue lysates, Lane 6: mouse RAW264.7 whole cell lysates, Lane 7: mouse EL-4 whole cell lysates, Lane 8: mouse Ana-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ING2 antigen affinity purified polyclonal antibody (Catalog # A04290-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ING2 at approximately 37 kDa. The expected band size for ING2 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04290-3-ing2-primary-antibodies-if-testing-2.jpgAnti-ING2 Antibody Picoband® IF analysis of ING2 using anti-ING2 antibody (A04290-3) and anti-Beta Tubulin antibody (M01857-3). ING2 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ING2 Antibody (A04290-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04290-3-ing2-primary-antibodies-fcm-testing-3.pngAnti-ING2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ING2 antibody (A04290-3). Overlay histogram showing HepG2 cells stained with A04290-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ING2 Antibody (A04290-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-insig1-picoband-trade-antibody-a02026-2-boster.html2026-03-17T05:15:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02026-2-insig1-primary-antibodies-wb-testing-1.jpgAnti-INSIG1 Antibody Picoband® Western blot analysis of INSIG1 using anti-INSIG1 antibody (A02026-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HUH7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INSIG1 antigen affinity purified polyclonal antibody (Catalog # A02026-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INSIG1 at approximately 66 kDa. The expected band size for INSIG1 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02026-2-insig1-primary-antibodies-ihc-testing-2.jpgAnti-INSIG1 Antibody Picoband® IHC analysis of INSIG1 using anti-INSIG1 antibody (A02026-2). INSIG1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INSIG1 Antibody (A02026-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02026-2-insig1-primary-antibodies-if-testing-3.jpgAnti-INSIG1 Antibody Picoband® IF analysis of INSIG1 using anti-INSIG1 antibody (A02026-2). INSIG1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-INSIG1 Antibody (A02026-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02026-2-insig1-primary-antibodies-fcm-testing-4.pngAnti-INSIG1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-INSIG1 antibody (A02026-2). Overlay histogram showing MCF-7 cells stained with A02026-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-INSIG1 Antibody (A02026-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-vegfr-1-flt1-picoband-trade-antibody-a00534-5-boster.html2026-03-16T09:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00534-5-flt1-primary-antibodies-wb-testing-1.jpgAnti-VEGFR-1/FLT1 Antibody Picoband® Western blot analysis of VEGFR-1/FLT1 using anti-VEGFR-1/FLT1 antibody (A00534-5). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VEGFR-1/FLT1 antigen affinity purified polyclonal antibody (Catalog # A00534-5) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VEGFR-1/FLT1 at approximately 200 kDa. The expected band size for VEGFR-1/FLT1 is at 151 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-padi3-picoband-trade-antibody-a11754-1-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11754-1-padi3-primary-antibodies-wb-testing-1.jpgAnti-PADI3 Antibody Picoband® Western blot analysis of PADI3 using anti-PADI3 antibody (A11754-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse kidney tissue lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PADI3 antigen affinity purified polyclonal antibody (Catalog # A11754-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PADI3 at approximately 75 kDa. The expected band size for PADI3 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11754-1-padi3-primary-antibodies-if-testing-2.jpgAnti-PADI3 Antibody Picoband® IF analysis of PADI3 using anti-PADI3 antibody (A11754-1). PADI3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PADI3 Antibody (A11754-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11754-1-padi3-primary-antibodies-fcm-testing-3.pngAnti-PADI3 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PADI3 antibody (A11754-1). Overlay histogram showing SH-SY5Y cells stained with A11754-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PADI3 Antibody (A11754-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lis1-pafah1b1-picoband-trade-antibody-a01273-1-boster.html2026-03-16T09:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01273-1-pafah1b1-primary-antibodies-wb-testing-1.jpgAnti-LIS1/PAFAH1B1 Antibody Picoband® Western blot analysis of LIS1/PAFAH1B1 using anti-LIS1/PAFAH1B1 antibody (A01273-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U87 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIS1/PAFAH1B1 antigen affinity purified polyclonal antibody (Catalog # A01273-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIS1/PAFAH1B1 at approximately 47 kDa. The expected band size for LIS1/PAFAH1B1 is at 47 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-rab3ip-picoband-trade-antibody-a09085-3-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09085-3-rab3ip-primary-antibodies-wb-testing-1.jpgAnti-RAB3IP Antibody Picoband® Western blot analysis of RAB3IP using anti-RAB3IP antibody (A09085-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB3IP antigen affinity purified polyclonal antibody (Catalog # A09085-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAB3IP at approximately 55 kDa. The expected band size for RAB3IP is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09085-3-rab3ip-primary-antibodies-ihc-testing-2.jpgAnti-RAB3IP Antibody Picoband® IHC analysis of RAB3IP using anti-RAB3IP antibody (A09085-3). RAB3IP was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB3IP Antibody (A09085-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09085-3-rab3ip-primary-antibodies-ihc-testing-3.jpgAnti-RAB3IP Antibody Picoband® IHC analysis of RAB3IP using anti-RAB3IP antibody (A09085-3). RAB3IP was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB3IP Antibody (A09085-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09085-3-rab3ip-primary-antibodies-ihc-testing-4.jpgAnti-RAB3IP Antibody Picoband® IHC analysis of RAB3IP using anti-RAB3IP antibody (A09085-3). RAB3IP was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB3IP Antibody (A09085-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09085-3-rab3ip-primary-antibodies-ihc-testing-5.jpgAnti-RAB3IP Antibody Picoband® IHC analysis of RAB3IP using anti-RAB3IP antibody (A09085-3). RAB3IP was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB3IP Antibody (A09085-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09085-3-rab3ip-primary-antibodies-fcm-testing-6.pngAnti-RAB3IP Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-RAB3IP antibody (A09085-3). Overlay histogram showing MCF-7 cells stained with A09085-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAB3IP Antibody (A09085-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-parp3-picoband-trade-antibody-a03762-2-boster.html2026-03-16T09:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03762-2-parp3-primary-antibodies-wb-testing-1.jpgAnti-PARP3 Antibody Picoband® Western blot analysis of PARP3 using anti-PARP3 antibody (A03762-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: monkey COS-7 whole cell lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARP3 antigen affinity purified polyclonal antibody (Catalog # A03762-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARP3 at approximately 60 kDa. The expected band size for PARP3 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03762-2-parp3-primary-antibodies-ihc-testing-2.jpgAnti-PARP3 Antibody Picoband® IHC analysis of PARP3 using anti-PARP3 antibody (A03762-2). PARP3 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PARP3 Antibody (A03762-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03762-2-parp3-primary-antibodies-ihc-testing-3.jpgAnti-PARP3 Antibody Picoband® IHC analysis of PARP3 using anti-PARP3 antibody (A03762-2). PARP3 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PARP3 Antibody (A03762-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03762-2-parp3-primary-antibodies-ihc-testing-4.jpgAnti-PARP3 Antibody Picoband® IHC analysis of PARP3 using anti-PARP3 antibody (A03762-2). PARP3 was detected in a paraffin-embedded section of rat lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PARP3 Antibody (A03762-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03762-2-parp3-primary-antibodies-if-testing-5.jpgAnti-PARP3 Antibody Picoband® IF analysis of PARP3 using anti-PARP3 antibody (A03762-2) and anti-Beta Tubulin antibody (M01857-3). PARP3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PARP3 Antibody (A03762-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-parp10-picoband-trade-antibody-a08514-2-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08514-2-parp10-primary-antibodies-wb-testing-1.jpgAnti-PARP10 Antibody Picoband® Western blot analysis of PARP10 using anti-PARP10 antibody (A08514-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARP10 antigen affinity purified polyclonal antibody (Catalog # A08514-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARP10 at approximately 140 kDa. The expected band size for PARP10 is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08514-2-parp10-primary-antibodies-fcm-testing-2.pngAnti-PARP10 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PARP10 antibody (A08514-2). Overlay histogram showing MCF-7 cells stained with A08514-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PARP10 Antibody (A08514-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pyruvate-carboxylase-pc-picoband-trade-antibody-a03853-3-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-wb-testing-1.jpgAnti-Pyruvate Carboxylase/PC Antibody Picoband® Western blot analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Pyruvate Carboxylase/PC antigen affinity purified polyclonal antibody (Catalog # A03853-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Pyruvate Carboxylase/PC at approximately 125 kDa. The expected band size for Pyruvate Carboxylase/PC is at 130 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-ihc-testing-2.jpgAnti-Pyruvate Carboxylase/PC Antibody Picoband® IHC analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Pyruvate Carboxylase/PC was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-ihc-testing-3.jpgAnti-Pyruvate Carboxylase/PC Antibody Picoband® IHC analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Pyruvate Carboxylase/PC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-ihc-testing-4.jpgAnti-Pyruvate Carboxylase/PC Antibody Picoband® IHC analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Pyruvate Carboxylase/PC was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-ihc-testing-5.jpgAnti-Pyruvate Carboxylase/PC Antibody Picoband® IHC analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Pyruvate Carboxylase/PC was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-ihc-testing-6.jpgAnti-Pyruvate Carboxylase/PC Antibody Picoband® IHC analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Pyruvate Carboxylase/PC was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-if-testing-7.jpgAnti-Pyruvate Carboxylase/PC Antibody Picoband® IF analysis of Pyruvate Carboxylase/PC using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Pyruvate Carboxylase/PC was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03853-3-pc-primary-antibodies-fcm-testing-8.pngAnti-Pyruvate Carboxylase/PC Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-Pyruvate Carboxylase/PC antibody (A03853-3). Overlay histogram showing MCF-7 cells stained with A03853-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Pyruvate Carboxylase/PC Antibody (A03853-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pdk1-picoband-trade-antibody-a01268-3-boster.html2026-03-16T09:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01268-3-pdk1-primary-antibodies-wb-testing-1.jpgAnti-PDK1 Antibody Picoband® Western blot analysis of PDK1 using anti-PDK1 antibody (A01268-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: rat RH35 whole cell lysates, Lane 4: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDK1 antigen affinity purified polyclonal antibody (Catalog # A01268-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDK1 at approximately 46 kDa. The expected band size for PDK1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01268-3-pdk1-primary-antibodies-fcm-testing-2.pngAnti-PDK1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PDK1 antibody (A01268-3). Overlay histogram showing 293T cells stained with A01268-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDK1 Antibody (A01268-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pdk3-picoband-trade-antibody-a05658-1-boster.html2026-03-17T05:13:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05658-1-pdk3-primary-antibodies-wb-testing-1.jpgAnti-PDK3 Antibody Picoband® Western blot analysis of PDK3 using anti-PDK3 antibody (A05658-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human SiHa whole cell lysates, Lane 5: human Jurkat whole cell lysates, Lane 6: human U251 whole cell lysates, Lane 7: human A549 whole cell lysates, Lane 8: rat testis tissue lysates, Lane 9: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDK3 antigen affinity purified polyclonal antibody (Catalog # A05658-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDK3 at approximately 47 kDa. The expected band size for PDK3 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05658-1-pdk3-primary-antibodies-ihc-testing-2.jpgAnti-PDK3 Antibody Picoband® IHC analysis of PDK3 using anti-PDK3 antibody (A05658-1). PDK3 was detected in a paraffin-embedded section of human meningioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDK3 Antibody (A05658-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05658-1-pdk3-primary-antibodies-ihc-testing-3.jpgAnti-PDK3 Antibody Picoband® IHC analysis of PDK3 using anti-PDK3 antibody (A05658-1). PDK3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDK3 Antibody (A05658-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05658-1-pdk3-primary-antibodies-ihc-testing-4.jpgAnti-PDK3 Antibody Picoband® IHC analysis of PDK3 using anti-PDK3 antibody (A05658-1). PDK3 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDK3 Antibody (A05658-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05658-1-pdk3-primary-antibodies-ihc-testing-5.jpgAnti-PDK3 Antibody Picoband® IHC analysis of PDK3 using anti-PDK3 antibody (A05658-1). PDK3 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDK3 Antibody (A05658-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05658-1-pdk3-primary-antibodies-if-testing-6.jpgAnti-PDK3 Antibody Picoband® IF analysis of PDK3 using anti-PDK3 antibody (A05658-1). PDK3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PDK3 Antibody (A05658-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05658-1-pdk3-primary-antibodies-fcm-testing-7.pngAnti-PDK3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-PDK3 antibody (A05658-1). Overlay histogram showing U251 cells stained with A05658-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDK3 Antibody (A05658-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-peli2-picoband-trade-antibody-a10176-1-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10176-1-peli2-primary-antibodies-wb-testing-1.jpgAnti-PELI2 Antibody Picoband® Western blot analysis of PELI2 using anti-PELI2 antibody (A10176-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human Ramos whole cell lysates, Lane 3: rat spleen tissue lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PELI2 antigen affinity purified polyclonal antibody (Catalog # A10176-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PELI2 at approximately 50 kDa. The expected band size for PELI2 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10176-1-peli2-primary-antibodies-ihc-testing-2.jpgAnti-PELI2 Antibody Picoband® IHC analysis of PELI2 using anti-PELI2 antibody (A10176-1). PELI2 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI2 Antibody (A10176-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10176-1-peli2-primary-antibodies-ihc-testing-3.jpgAnti-PELI2 Antibody Picoband® IHC analysis of PELI2 using anti-PELI2 antibody (A10176-1). PELI2 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI2 Antibody (A10176-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10176-1-peli2-primary-antibodies-ihc-testing-4.jpgAnti-PELI2 Antibody Picoband® IHC analysis of PELI2 using anti-PELI2 antibody (A10176-1). PELI2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI2 Antibody (A10176-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10176-1-peli2-primary-antibodies-if-testing-5.jpgAnti-PELI2 Antibody Picoband® IF analysis of PELI2 using anti-PELI2 antibody (A10176-1). PELI2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PELI2 Antibody (A10176-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10176-1-peli2-primary-antibodies-fcm-testing-6.pngAnti-PELI2 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-PELI2 antibody (A10176-1). Overlay histogram showing THP-1 cells stained with A10176-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PELI2 Antibody (A10176-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-peli3-picoband-trade-antibody-a09622-1-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-wb-testing-1.jpgAnti-PELI3 Antibody Picoband® Western blot analysis of PELI3 using anti-PELI3 antibody (A09622-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat heart tissue lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PELI3 antigen affinity purified polyclonal antibody (Catalog # A09622-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PELI3 at approximately 51 kDa. The expected band size for PELI3 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-2.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of human ovarian serous adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-3.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-4.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-5.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-6.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-7.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-8.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-ihc-testing-9.jpgAnti-PELI3 Antibody Picoband® IHC analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-if-testing-10.jpgAnti-PELI3 Antibody Picoband® IF analysis of PELI3 using anti-PELI3 antibody (A09622-1). PELI3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PELI3 Antibody (A09622-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09622-1-peli3-primary-antibodies-fcm-testing-11.pngAnti-PELI3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PELI3 antibody (A09622-1). Overlay histogram showing HepG2 cells stained with A09622-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PELI3 Antibody (A09622-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcf11-picoband-trade-antibody-a05372-1-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05372-1-pcf11-primary-antibodies-wb-testing-1.jpgAnti-PCF11 Antibody Picoband® Western blot analysis of PCF11 using anti-PCF11 antibody (A05372-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCF11 antigen affinity purified polyclonal antibody (Catalog # A05372-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCF11 at approximately 200 kDa. The expected band size for PCF11 is at 173 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-txnip-picoband-trade-antibody-a01409-3-boster.html2026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01409-3-txnip-primary-antibodies-wb-testing-1.jpgAnti-TXNIP Antibody Picoband® Western blot analysis of TXNIP using anti-TXNIP antibody (A01409-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TXNIP antigen affinity purified polyclonal antibody (Catalog # A01409-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TXNIP at approximately 50-55 kDa. The expected band size for TXNIP is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01409-3-txnip-primary-antibodies-fcm-testing-2.pngAnti-TXNIP Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-TXNIP antibody (A01409-3). Overlay histogram showing MCF-7 cells stained with A01409-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TXNIP Antibody (A01409-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-odc1-dz41450-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-foxl2-dz41451-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-fmo3-dz41452-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-p63-dz41453-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-laminin-loc582206-beta-1-dz41454-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-pks1-dz41455-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-bat-star-lamin-b1-dz41460-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-bat-star-prelamin-a-c-dz41461-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-mallard-piezo2-dz41467-boster.html2026-03-10T04:36:46+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251842026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251852026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00964-2-myod1-primary-antibodies-wb-testing-1.jpgAnti-MYOD1 Antibody Picoband®Western blot analysis of MYOD1 using anti-MYOD1 antibody (A00964-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RD whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: rat skeletal muscle tissue lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYOD1 antigen affinity purified polyclonal antibody (A00964-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MYOD1 at approximately 35-45 kDa. The expected band size for MYOD1 is at 35 kDa. https://www.bosterbio.com/catalog/product/view/id/1251862026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251872026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251882026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-wb-testing-1.jpgAnti-WWTR1 Antibody Picoband® Western blot analysis of WWTR1 using anti-WWTR1 antibody (A02672-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-WWTR1 antigen affinity purified polyclonal antibody (A02672-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for WWTR1 at approximately 50 kDa. The expected band size for WWTR1 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-ihc-testing-1.jpgAnti-WWTR1 Antibody Picoband® IHC analysis of WWTR1 using anti-WWTR1 antibody (A02672-2). WWTR1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-WWTR1 Antibody (A02672-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-ihc-testing-2.jpgAnti-WWTR1 Antibody Picoband® IHC analysis of WWTR1 using anti-WWTR1 antibody (A02672-2). WWTR1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-WWTR1 Antibody (A02672-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-ihc-testing-3.jpgAnti-WWTR1 Antibody Picoband® IHC analysis of WWTR1 using anti-WWTR1 antibody (A02672-2). WWTR1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-WWTR1 Antibody (A02672-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-ihc-testing-4.jpgAnti-WWTR1 Antibody Picoband® IHC analysis of WWTR1 using anti-WWTR1 antibody (A02672-2). WWTR1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-WWTR1 Antibody (A02672-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-ihc-testing-5.jpgAnti-WWTR1 Antibody Picoband® IHC analysis of WWTR1 using anti-WWTR1 antibody (A02672-2). WWTR1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-WWTR1 Antibody (A02672-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-if-testing-1.jpgAnti-WWTR1 Antibody Picoband® IF analysis of WWTR1 using anti-WWTR1 antibody (A02672-2) and anti-Alpha Tubulin antibody (M03989-3). WWTR1 was detected in an immunocytochemical section of U251 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-WWTR1 Antibody (A02672-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02672-2-wwtr1-primary-antibodies-ip-testing-1.jpgAnti-WWTR1 Antibody Picoband® Immunoprecipitating WWTR1 in Hela whole cell lysate. Western blot analysis of WWTR1 using anti-WWTR1 antibody (A02672-2). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-WWTR1 antibody in Hela whole cell lysate, Lane 3: anti-WWTR1 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-WWTR1 antigen affinity purified polyclonal antibody (A02672-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for WWTR1 at approximately 50 kDa. The expected band size for WWTR1 is at 44 kDa. https://www.bosterbio.com/catalog/product/view/id/1251892026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251902026-03-13T05:05:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01433-3-cdc25a-primary-antibodies-ihc-testing-1.jpgAnti-CDC25A AntibodyIHC analysis of CDC25A using anti-CDC25A antibody (A01433-3). CDC25A was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CDC25A Antibody (A01433-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01433-3-cdc25a-primary-antibodies-ihc-testing-2.jpgAnti-CDC25A AntibodyIHC analysis of CDC25A using anti-CDC25A antibody (A01433-3). CDC25A was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CDC25A Antibody (A01433-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1251912026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251922026-03-16T05:08:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06405-1-atp8-mt-atp8-primary-antibodies-wb-testing-1.jpgAnti-ATP8/MT-ATP8 Antibody Western blot analysis of ATP8/MT-ATP8 using anti-ATP8/MT-ATP8 antibody (A06405-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Lncap whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP8/MT-ATP8 antigen affinity purified polyclonal antibody (A06405-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ATP8/MT-ATP8 at approximately 12 kDa. The expected band size for ATP8/MT-ATP8 is at 8 kDa. https://www.bosterbio.com/catalog/product/view/id/1251932026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-wb-testing-1_1.jpgAnti-ABCG5 AntibodyWestern blot analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human Ramos whole cell lysates, Lane 4: human HUH7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse HEPA1/6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCG5 antigen affinity purified polyclonal antibody (A01503-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ABCG5 at approximately 73 kDa. The expected band size for ABCG5 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-ihc-testing-1.jpgAnti-ABCG5 AntibodyIHC analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). ABCG5 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCG5 Antibody (A01503-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-ihc-testing-2_1.jpgAnti-ABCG5 AntibodyIHC analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). ABCG5 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCG5 Antibody (A01503-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-ihc-testing-3.jpgAnti-ABCG5 AntibodyIHC analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). ABCG5 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCG5 Antibody (A01503-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-ihc-testing-4.jpgAnti-ABCG5 AntibodyIHC analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). ABCG5 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCG5 Antibody (A01503-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-if-testing-1.jpgAnti-ABCG5 AntibodyIF analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). ABCG5 was detected in an immunocytochemical section of CACO-2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ABCG5 Antibody (A01503-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-if-testing-2.jpgAnti-ABCG5 AntibodyIF analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). ABCG5 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ABCG5 Antibody (A01503-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-if-testing-3.jpgAnti-ABCG5 AntibodyIF analysis of ABCG5 using anti-ABCG5 antibody (A01503-2). ABCG5 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ABCG5 Antibody (A01503-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01503-2-abcg5-primary-antibodies-ip-testing-1.jpgAnti-ABCG5 AntibodyImmunoprecipitating (IP) ABCG5 in HepG2 whole cell lysate. Western blot analysis of ABCG5 using anti-ABCG5 antibody (A01503-2); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-ABCG5 antibody in HepG2 whole cell lysate; Lane 3: anti-ABCG5 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ABCG5 antigen affinity purified polyclonal antibody (A01503-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for ABCG5 at approximately 73 kDa. The expected band size for ABCG5 is at 73 kDa. https://www.bosterbio.com/catalog/product/view/id/1251942026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06374-2-ctps1-primary-antibodies-wb-testing-1.jpgAnti-CTPS1 Antibody Picoband®Western blot analysis of CTPS1 using anti-CTPS1 antibody (A06374-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTPS1 antigen affinity purified polyclonal antibody (A06374-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CTPS1 at approximately 75 kDa. The expected band size for CTPS1 is at 67 kDa. https://www.bosterbio.com/catalog/product/view/id/1251952026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251962026-03-13T05:05:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-wb-testing-1.jpgAnti-CD98/SLC3A2 Antibody Western blot analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD98/SLC3A2 antigen affinity purified polyclonal antibody (A01794-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CD98/SLC3A2 at approximately 75-120 kDa. The expected band size for CD98/SLC3A2 is at 68,71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-ihc-testing-6.jpgAnti-CD98/SLC3A2 Antibody IHC analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). CD98/SLC3A2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD98/SLC3A2 Antibody (A01794-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-ihc-testing-7.jpgAnti-CD98/SLC3A2 Antibody IHC analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). CD98/SLC3A2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD98/SLC3A2 Antibody (A01794-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-ihc-testing-5.jpgAnti-CD98/SLC3A2 Antibody IHC analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). CD98/SLC3A2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD98/SLC3A2 Antibody (A01794-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-ihc-testing-4.jpgAnti-CD98/SLC3A2 Antibody IHC analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). CD98/SLC3A2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD98/SLC3A2 Antibody (A01794-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-ihc-testing-3.jpgAnti-CD98/SLC3A2 Antibody IHC analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). CD98/SLC3A2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD98/SLC3A2 Antibody (A01794-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-ihc-testing-2.jpgAnti-CD98/SLC3A2 Antibody IHC analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). CD98/SLC3A2 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CD98/SLC3A2 Antibody (A01794-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01794-4-cd98-slc3a2-primary-antibodies-if-testing-1.jpgAnti-CD98/SLC3A2 AntibodyIF analysis of CD98/SLC3A2 using anti-CD98/SLC3A2 antibody (A01794-4). CD98/SLC3A2 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-CD98/SLC3A2 Antibody (A01794-4) overnight at 4°C. Fluoro®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1251972026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251982026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1251992026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252002026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252012026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252022026-03-13T05:05:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02331-3-vamp2-primary-antibodies-wb-testing-1.jpgAnti-VAMP2 AntibodyWestern blot analysis of VAMP2 using anti-VAMP2 antibody (A02331-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat hippocampus tissue lysates, Lane 3: mouse brain tissue lysates, Lane 4: mouse hippocampus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VAMP2 antigen affinity purified polyclonal antibody (A02331-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VAMP2 at approximately 19 kDa. The expected band size for VAMP2 is at 13 kDa. https://www.bosterbio.com/catalog/product/view/id/1252032026-03-16T05:08:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06384-2-vps16-primary-antibodies-wb-testing-1.jpgAnti-VPS16 Antibody Western blot analysis of VPS16 using anti-VPS16 antibody (A06384-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VPS16 antigen affinity purified polyclonal antibody (A06384-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VPS16 at approximately 95 kDa. The expected band size for VPS16 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06384-2-vps16-primary-antibodies-ihc-testing-1.jpgAnti-VPS16 AntibodyIHC analysis of VPS16 using anti-VPS16 antibody (A06384-2). VPS16 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-VPS16 Antibody (A06384-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1252042026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252052026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252062026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252072026-03-13T05:05:04+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252082026-03-16T05:08:23+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252092026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252102026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252112026-03-13T05:05:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-wb-testing-1.jpgAnti-HNRNPC AntibodyWestern blot analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HNRNPC antigen affinity purified polyclonal antibody (A02726-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HNRNPC at approximately 38, 41 kDa. The expected band size for HNRNPC is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-1.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of human bladder urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-2.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-3.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of human testicular cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-4.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-5.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-6.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of human intestinal diffuse large B-cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-7.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-8.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-ihc-testing-9.jpgAnti-HNRNPC AntibodyIHC analysis of HNRNPC using anti-HNRNPC antibody (A02726-1). HNRNPC was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-if-testing-1.jpgAnti-HNRNPC AntibodyIF analysis of HNRNPC using anti-HNRNPC antibody (A02726-1) and anti-Tubulin Alpha antibody (M03989-3). HNRNPC was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-HNRNPC Antibody (A02726-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02726-1-hnrnpc-primary-antibodies-fcm-testing-1.jpgAnti-HNRNPC AntibodyFlow Cytometry analysis of U2OS cells using anti-HNRNPC antibody (A02726-1). Overlay histogram showing U2OS cells stained with A02726-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HNRNPC Antibody (A02726-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1252122026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252132026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252142026-03-17T05:15:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01723-3-pak4-primary-antibodies-wb-testing-1.jpgAnti-PAK4 Antibody Picoband®Western blot analysis of PAK4 using anti-PAK4 antibody (A01723-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAK4 antigen affinity purified polyclonal antibody (A01723-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PAK4 at approximately 64 kDa. The expected band size for PAK4 is at 64 kDa. https://www.bosterbio.com/catalog/product/view/id/1252152026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252162026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06591-2-tgoln2-primary-antibodies-wb-testing-1.jpgAnti-TGN46/TGOLN2 Antibody Picoband®Western blot analysis of TGN46/TGOLN2 using anti-TGN46/TGOLN2 antibody (A06591-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TGN46/TGOLN2 antigen affinity purified polyclonal antibody (A06591-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TGN46/TGOLN2 at approximately 90-100 kDa. The expected band size for TGN46/TGOLN2 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06591-2-tgoln2-primary-antibodies-ihc-testing-1.jpgAnti-TGN46/TGOLN2 Antibody Picoband®IHC analysis of TGOLN2 using anti-TGOLN2 antibody (A06591-2). TGOLN2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TGOLN2 Antibody (A06591-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06591-2-tgoln2-primary-antibodies-ihc-testing-2.jpgAnti-TGN46/TGOLN2 Antibody Picoband®IHC analysis of TGOLN2 using anti-TGOLN2 antibody (A06591-2). TGOLN2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TGOLN2 Antibody (A06591-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06591-2-tgoln2-primary-antibodies-ihc-testing-3.jpgAnti-TGN46/TGOLN2 Antibody Picoband®IHC analysis of TGOLN2 using anti-TGOLN2 antibody (A06591-2). TGOLN2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TGOLN2 Antibody (A06591-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06591-2-tgoln2-primary-antibodies-if-testing-1.jpgAnti-TGN46/TGOLN2 Antibody Picoband®IF analysis of TGOLN2 using anti-TGOLN2 antibody (A06591-2). TGOLN2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TGOLN2 Antibody (A06591-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06591-2-tgoln2-primary-antibodies-fcm-testing-1.jpgAnti-TGN46/TGOLN2 Antibody Picoband®Flow Cytometry analysis of U937 cells using anti-TGN46/TGOLN2 antibody (A06591-2). Overlay histogram showing U937 cells stained with A06591-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TGN46/TGOLN2 Antibody (A06591-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1252172026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252182026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252192026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252202026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252212026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252222026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10425-1-trim31-primary-antibodies-wb-testing-1.jpgAnti-TRIM31 Antibody Picoband®Western blot analysis of TRIM31 using anti-TRIM31 antibody (A10425-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: rat stomach tissue lysates, Lane 5: mouse small intestine tissue lysates, Lane 6: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIM31 antigen affinity purified polyclonal antibody (A10425-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIM31 at approximately 48 kDa. The expected band size for TRIM31 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10425-1-trim31-primary-antibodies-fcm-testing-1.jpgAnti-TRIM31 Antibody Picoband®Flow Cytometry analysis of CACO-2 cells using anti-TRIM31 antibody (A10425-1). Overlay histogram showing CACO-2 cells stained with A10425-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TRIM31 Antibody (A10425-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1252232026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252242026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252252026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252262026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252272026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252282026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252292026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252302026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252312026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02461-1-gsto1-primary-antibodies-wb-testing-1_1.jpgAnti-GSTO1 Antibody Picoband®Western blot analysis of GSTO1 using anti-GSTO1 antibody (A02461-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse brain tissue lysates, Lane 4: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSTO1 antigen affinity purified polyclonal antibody (A02461-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GSTO1 at approximately 30 kDa. The expected band size for GSTO1 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02461-1-gsto1-primary-antibodies-ihc-testing-1.jpgAnti-GSTO1 Antibody Picoband®IHC analysis of GSTO1 using anti-GSTO1 antibody (A02461-1). GSTO1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GSTO1 Antibody (A02461-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02461-1-gsto1-primary-antibodies-fcm-testing-1.jpgAnti-GSTO1 Antibody Picoband®Flow Cytometry analysis of C2C12 cells using anti-GSTO1 antibody (A02461-1). Overlay histogram showing C2C12 cells stained with A02461-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GSTO1 Antibody (A02461-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02461-1-gsto1-primary-antibodies-ihc-testing-2.jpgAnti-GSTO1 Antibody Picoband®IHC analysis of GSTO1 using anti-GSTO1 antibody (A02461-1). GSTO1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GSTO1 Antibody (A02461-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1252322026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252332026-03-16T05:08:24+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252342026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252352026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252362026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252372026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252382026-03-13T05:05:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00948-2-map4-primary-antibodies-wb-testing-1.jpgAnti-MAP4 Antibody Western blot analysis of MAP4 using anti-MAP4 antibody (A00948-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP4 antigen affinity purified polyclonal antibody (A00948-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MAP4 at approximately 210 kDa. The expected band size for MAP4 is at 121 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00948-2-map4-primary-antibodies-ihc-testing-2.jpgAnti-MAP4 Antibody IHC analysis of MAP4 using anti-MAP4 antibody (A00948-2). MAP4 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MAP4 Antibody (A00948-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1252392026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252402026-03-16T05:08:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08683-1-mical2-primary-antibodies-wb-testing-1.jpgAnti-MICAL2 Antibody Western blot analysis of MICAL2 using anti-MICAL2 antibody (A08683-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human U-87MG whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat lung tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MICAL2 antigen affinity purified polyclonal antibody (A08683-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MICAL2 at approximately 95 kDa. The expected band size for MICAL2 is at 219 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08683-1-mical2-primary-antibodies-ihc-testing-2.jpgAnti-MICAL2 Antibody IHC analysis of MICAL2 using anti-MICAL2 antibody (A08683-1). MICAL2 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MICAL2 Antibody (A08683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08683-1-mical2-primary-antibodies-ihc-testing-3.jpgAnti-MICAL2 Antibody IHC analysis of MICAL2 using anti-MICAL2 antibody (A08683-1). MICAL2 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MICAL2 Antibody (A08683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08683-1-mical2-primary-antibodies-ihc-testing-4.jpgAnti-MICAL2 Antibody IHC analysis of MICAL2 using anti-MICAL2 antibody (A08683-1). MICAL2 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MICAL2 Antibody (A08683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1252412026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252422026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252432026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03025-1-pex1-primary-antibodies-wb-testing-1.jpgAnti-PEX1 Antibody Picoband®Western blot analysis of PEX1 using anti-PEX1 antibody (A03025-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PEX1 antigen affinity purified polyclonal antibody (A03025-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PEX1 at approximately 143 kDa. The expected band size for PEX1 is at 143 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03025-1-pex1-primary-antibodies-ihc-testing-1.jpgAnti-PEX1 Antibody Picoband®IHC analysis of PEX1 using anti-PEX1 antibody (A03025-1). PEX1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PEX1 Antibody (A03025-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03025-1-pex1-primary-antibodies-ihc-testing-2.jpgAnti-PEX1 Antibody Picoband®IHC analysis of PEX1 using anti-PEX1 antibody (A03025-1). PEX1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PEX1 Antibody (A03025-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03025-1-pex1-primary-antibodies-if-testing-1.jpgAnti-PEX1 Antibody Picoband®IF analysis of PEX1 using anti-PEX1 antibody (A03025-1). PEX1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PEX1 Antibody (A03025-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03025-1-pex1-primary-antibodies-fcm-testing-1.jpgAnti-PEX1 Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-PEX1 antibody (A03025-1). Overlay histogram showing SH-SY5Y cells stained with A03025-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PEX1 Antibody (A03025-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1252442026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252452026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252462026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252472026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252482026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252492026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252502026-03-16T05:08:25+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252512026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252522026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01474-1-slc1a5-primary-antibodies-wb-testing-1.jpgAnti-ASCT2/SLC1A5 Antibody Picoband®Western blot analysis of SLC1A5 using anti-SLC1A5 antibody (A01474-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC1A5 antigen affinity purified polyclonal antibody (A01474-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC1A5 at approximately 55-70 kDa. The expected band size for SLC1A5 is at 57 kDa. https://www.bosterbio.com/catalog/product/view/id/1252532026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252542026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-wb-testing-1.jpgAnti-CCPG1 Antibody Picoband® Western blot analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCPG1 antigen affinity purified polyclonal antibody (A11765-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CCPG1 at approximately 100-110 kDa. The expected band size for CCPG1 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-ihc-testing-2.jpgAnti-CCPG1 Antibody Picoband® IHC analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). CCPG1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CCPG1 Antibody (A11765-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-ihc-testing-3.jpgAnti-CCPG1 Antibody Picoband® IHC analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). CCPG1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CCPG1 Antibody (A11765-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-ihc-testing-4.jpgAnti-CCPG1 Antibody Picoband® IHC analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). CCPG1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CCPG1 Antibody (A11765-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-ihc-testing-5.jpgAnti-CCPG1 Antibody Picoband® IHC analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). CCPG1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CCPG1 Antibody (A11765-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-ihc-testing-6.jpgAnti-CCPG1 Antibody Picoband® IHC analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). CCPG1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CCPG1 Antibody (A11765-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-ihc-testing-7.jpgAnti-CCPG1 Antibody Picoband® IHC analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). CCPG1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CCPG1 Antibody (A11765-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-wb-testing-1_1.jpgAnti-CCPG1 Antibody Picoband®Western blot analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCPG1 antigen affinity purified polyclonal antibody (A11765-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CCPG1 at approximately 110 kDa. The expected band size for CCPG1 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11765-2-ccpg1-primary-antibodies-if-testing-1.jpgAnti-CCPG1 Antibody Picoband®IF analysis of CCPG1 using anti-CCPG1 antibody (A11765-2). CCPG1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CCPG1 Antibody (A11765-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1252552026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252562026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252572026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252582026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252592026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252602026-03-16T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10074-2-cdca3-primary-antibodies-ihc-testing-1.jpgAnti-CDCA3 Antibody IHC analysis of CDCA3 using anti-CDCA3 antibody (A10074-2). CDCA3 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CDCA3 Antibody (A10074-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10074-2-cdca3-primary-antibodies-ihc-testing-2.jpgAnti-CDCA3 Antibody IHC analysis of CDCA3 using anti-CDCA3 antibody (A10074-2). CDCA3 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CDCA3 Antibody (A10074-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1252612026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252622026-03-13T05:05:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02626-1-usp8-primary-antibodies-wb-testing-1.jpgAnti-USP8 AntibodyWestern blot analysis of USP8 using anti-USP8 antibody (A02626-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-USP8 antigen affinity purified polyclonal antibody (A02626-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for USP8 at approximately 130 kDa. The expected band size for USP8 is at 128 kDa. https://www.bosterbio.com/catalog/product/view/id/1252632026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252642026-03-16T05:08:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04274-1-zbtb20-primary-antibodies-wb-testing-1.jpgAnti-ZBTB20 Antibody Western blot analysis of ZBTB20 using anti-ZBTB20 antibody (A04274-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human U2OS whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ZBTB20 antigen affinity purified polyclonal antibody (A04274-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ZBTB20 at approximately 73 kDa. The expected band size for ZBTB20 is at 73, 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04274-1-zbtb20-primary-antibodies-ihc-testing-2.jpgAnti-ZBTB20 Antibody IHC analysis of ZBTB20 using anti-ZBTB20 antibody (A04274-1). ZBTB20 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ZBTB20 Antibody (A04274-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04274-1-zbtb20-primary-antibodies-ihc-testing-3.jpgAnti-ZBTB20 Antibody IHC analysis of ZBTB20 using anti-ZBTB20 antibody (A04274-1). ZBTB20 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-ZBTB20 Antibody (A04274-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04274-1-zbtb20-primary-antibodies-ihc-testing-4.jpgAnti-ZBTB20 AntibodyIHC analysis of ZBTB20 using anti-ZBTB20 antibody (A04274-1). ZBTB20 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ZBTB20 Antibody (A04274-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1252652026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252662026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252672026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252682026-03-16T05:08:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252692026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252702026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252712026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-wb-testing-1.jpgAnti-VHL Antibody Picoband® Western blot analysis of VHL using anti-VHL antibody (A00079-3). Electrophoresis was performed on a 13% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VHL antigen affinity purified polyclonal antibody (A00079-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VHL at approximately 18 kDa. The expected band size for VHL is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-ihc-testing-2.jpgAnti-VHL Antibody Picoband® IHC analysis of VHL using anti-VHL antibody (A00079-3). VHL was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VHL Antibody (A00079-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-wb-testing-1_1.jpgAnti-VHL Antibody Picoband®Western blot analysis of VHL using anti-VHL antibody (A00079-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VHL antigen affinity purified polyclonal antibody (A00079-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for VHL at approximately 24 kDa. The expected band size for VHL is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-ihc-testing-1.jpgAnti-VHL Antibody Picoband®IHC analysis of VHL using anti-VHL antibody (A00079-3). VHL was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-VHL Antibody (A00079-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-ihc-testing-2_1.jpgAnti-VHL Antibody Picoband®IHC analysis of VHL using anti-VHL antibody (A00079-3). VHL was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-VHL Antibody (A00079-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-if-testing-1_1.jpgAnti-VHL Antibody Picoband®IF analysis of VHL using anti-VHL antibody (A00079-3). VHL was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-VHL Antibody (A00079-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-fcm-testing-1.jpgAnti-VHL Antibody Picoband®Flow Cytometry analysis of A549 cells using anti-VHL antibody (A00079-3). Overlay histogram showing A549 cells stained with A00079-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-VHL Antibody (A00079-3, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-fcm-testing-2.jpgAnti-VHL Antibody Picoband®Flow Cytometry analysis of RT4 cells using anti-VHL antibody (A00079-3). Overlay histogram showing RT4 cells stained with A00079-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-VHL Antibody (A00079-3, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-ihc-testing-3.jpgAnti-VHL Antibody Picoband®IHC analysis of VHL using anti-VHL antibody (A00079-3). VHL was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-VHL Antibody (A00079-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00079-3-vhl-primary-antibodies-if-testing-1.jpgAnti-VHL Antibody Picoband®IF analysis of VHL using anti-VHL antibody (A00079-3) and anti-Tubulin Alpha antibody (M03989-3). VHL was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-VHL Antibody (A00079-3) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1252722026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252732026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252742026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252752026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252762026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252772026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252782026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252792026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252802026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252812026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252822026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252832026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252842026-03-16T05:08:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10223-1-alg11-primary-antibodies-wb-testing-1.jpgAnti-ALG11 AntibodyWestern blot analysis of ALG11 using anti-ALG11 antibody (A10223-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALG11 antigen affinity purified polyclonal antibody (A10223-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALG11 at approximately 56 kDa. The expected band size for ALG11 is at 56 kDa. https://www.bosterbio.com/catalog/product/view/id/1252852026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252862026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252872026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252882026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252892026-03-13T05:05:05+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252902026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252912026-03-16T05:08:27+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252922026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252932026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252942026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252952026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252962026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252972026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1252982026-03-16T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04696-2-rpa3-primary-antibodies-wb-testing-1.jpgAnti-RPA3 AntibodyWestern blot analysis of RPA3 using anti-RPA3 antibody (A04696-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPA3 antigen affinity purified polyclonal antibody (A04696-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPA3 at approximately 14 kDa. The expected band size for RPA3 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04696-2-rpa3-primary-antibodies-ihc-testing-1.jpgAnti-RPA3 AntibodyIHC analysis of RPA3 using anti-RPA3 antibody (A04696-2). RPA3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-RPA3 Antibody (A04696-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-numb-picoband-trade-antibody-a01206-2-boster.html2026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01206-2-numb-primary-antibodies-wb-testing-1.jpgAnti-NUMB Antibody Picoband® Western blot analysis of NUMB using anti-NUMB antibody (A01206-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U-87 MG whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat brain tissue tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUMB antigen affinity purified polyclonal antibody (Catalog # A01206-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUMB at approximately 72-75 kDa. The expected band size for NUMB is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01206-2-numb-primary-antibodies-fcm-testing-2.pngAnti-NUMB Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-NUMB antibody (A01206-2). Overlay histogram showing RT4 cells stained with A01206-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUMB Antibody (A01206-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-bpnt2-picoband-trade-antibody-a11341-2-boster.html2026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-wb-testing-1.jpgAnti-BPNT2 Antibody Picoband® Western blot analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BPNT2 antigen affinity purified polyclonal antibody (Catalog # A11341-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BPNT2 at approximately 42 kDa. The expected band size for BPNT2 is at 39,42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-2.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-3.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-4.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-5.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of human meningioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-6.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-7.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-8.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-9.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-10.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-11.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-ihc-testing-12.jpgAnti-BPNT2 Antibody Picoband® IHC analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-if-testing-13.jpgAnti-BPNT2 Antibody Picoband® IF analysis of BPNT2 using anti-BPNT2 antibody (A11341-2). BPNT2 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BPNT2 Antibody (A11341-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11341-2-impad1-primary-antibodies-fcm-testing-14.pngAnti-BPNT2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-BPNT2 antibody (A11341-2). Overlay histogram showing HepG2 cells stained with A11341-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BPNT2 Antibody (A11341-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ing5-picoband-trade-antibody-a04974-3-boster.html2026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04974-3-ing5-primary-antibodies-wb-testing-1.jpgAnti-ING5 Antibody Picoband® Western blot analysis of ING5 using anti-ING5 antibody (A04974-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: monkey COS-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ING5 antigen affinity purified polyclonal antibody (Catalog # A04974-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ING5 at approximately 32 kDa. The expected band size for ING5 is at 28,32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04974-3-ing5-primary-antibodies-if-testing-2.jpgAnti-ING5 Antibody Picoband® IF analysis of ING5 using anti-ING5 antibody (A04974-3) and anti-Beta Tubulin antibody (M01857-3). ING5 was detected in immunocytochemical section of SiHa cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ING5 Antibody (A04974-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04974-3-ing5-primary-antibodies-fcm-testing-3.pngAnti-ING5 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-ING5 antibody (A04974-3). Overlay histogram showing JK cells stained with A04974-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ING5 Antibody (A04974-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ino80b-picoband-trade-antibody-a11475-1-boster.html2026-03-16T09:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11475-1-ino80b-primary-antibodies-wb-testing-1.jpgAnti-INO80B Antibody Picoband® Western blot analysis of INO80B using anti-INO80B antibody (A11475-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INO80B antigen affinity purified polyclonal antibody (Catalog # A11475-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INO80B at approximately 48 kDa. The expected band size for INO80B is at 39,50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11475-1-ino80b-primary-antibodies-fcm-testing-2.pngAnti-INO80B Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-INO80B antibody (A11475-1). Overlay histogram showing 293T cells stained with A11475-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-INO80B Antibody (A11475-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11475-1-ino80b-primary-antibodies-fcm-testing-3.pngAnti-INO80B Antibody Picoband® Flow Cytometry analysis of JK cells using anti-INO80B antibody (A11475-1). Overlay histogram showing JK cells stained with A11475-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-INO80B Antibody (A11475-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-inpp5d-picoband-trade-antibody-a03358-1-boster.html2026-03-16T09:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03358-1-inpp5d-primary-antibodies-wb-testing-1_1.jpgAnti-INPP5D Antibody Picoband® Western blot analysis of INPP5D using anti-INPP5D antibody (A03358-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INPP5D antigen affinity purified polyclonal antibody (Catalog # A03358-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INPP5D at approximately 145 kDa. The expected band size for INPP5D is at 133 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03358-1-inpp5d-primary-antibodies-ihc-testing-2.pngAnti-INPP5D Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-INPP5D antibody (A03358-1). Overlay histogram showing THP-1 cells stained with A03358-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-INPP5D Antibody (A03358-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-patz1-picoband-trade-antibody-a06823-1-boster.html2026-03-16T09:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06823-1-patz1-primary-antibodies-wb-testing-1.jpgAnti-PATZ1 Antibody Picoband® Western blot analysis of PATZ1 using anti-PATZ1 antibody (A06823-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PATZ1 antigen affinity purified polyclonal antibody (Catalog # A06823-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PATZ1 at approximately 70 kDa. The expected band size for PATZ1 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06823-1-patz1-primary-antibodies-if-testing-2.jpgAnti-PATZ1 Antibody Picoband® IF analysis of PATZ1 using anti-PATZ1 antibody (A06823-1) and anti-Beta Tubulin antibody (M01857-3). PATZ1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PATZ1 Antibody (A06823-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06823-1-patz1-primary-antibodies-fcm-testing-3.pngAnti-PATZ1 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PATZ1 antibody (A06823-1). Overlay histogram showing Hela cells stained with A06823-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PATZ1 Antibody (A06823-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdha6-picoband-trade-antibody-a13958-1-boster.html2026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13958-1-pcdha6-primary-antibodies-wb-testing-1.jpgAnti-PCDHA6 Antibody Picoband® Western blot analysis of PCDHA6 using anti-PCDHA6 antibody (A13958-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHA6 antigen affinity purified polyclonal antibody (Catalog # A13958-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHA6 at approximately 150 kDa. The expected band size for PCDHA6 is at 103,120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13958-1-pcdha6-primary-antibodies-fcm-testing-2.pngAnti-PCDHA6 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PCDHA6 antibody (A13958-1). Overlay histogram showing MCF-7 cells stained with A13958-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHA6 Antibody (A13958-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13958-1-pcdha6-primary-antibodies-fcm-testing-3.pngAnti-PCDHA6 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-PCDHA6 antibody (A13958-1). Overlay histogram showing PC-3 cells stained with A13958-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHA6 Antibody (A13958-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdha8-picoband-trade-antibody-a15533-boster.html2026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15533-pcdha8-primary-antibodies-wb-testing-1.jpgAnti-PCDHA8 Antibody Picoband® Western blot analysis of PCDHA8 using anti-PCDHA8 antibody (A15533). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHA8 antigen affinity purified polyclonal antibody (Catalog # A15533) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHA8 at approximately 150 kDa. The expected band size for PCDHA8 is at 103 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15533-pcdha8-primary-antibodies-fcm-testing-2.pngAnti-PCDHA8 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PCDHA8 antibody (A15533). Overlay histogram showing SH-SY5Y cells stained with A15533 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHA8 Antibody (A15533, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdha13-picoband-trade-antibody-a16196-1-boster.html2026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16196-1-pcdha13-primary-antibodies-wb-testing-1.jpgAnti-PCDHA13 Antibody Picoband® Western blot analysis of PCDHA13 using anti-PCDHA13 antibody (A16196-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHA13 antigen affinity purified polyclonal antibody (Catalog # A16196-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHA13 at approximately 102 kDa. The expected band size for PCDHA13 is at 99,102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16196-1-pcdha13-primary-antibodies-fcm-testing-2.pngAnti-PCDHA13 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-PCDHA13 antibody (A16196-1). Overlay histogram showing PC-3 cells stained with A16196-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHA13 Antibody (A16196-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-bcat2-picoband-trade-antibody-a06369-1-boster.html2026-03-17T05:15:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-wb-testing-1.jpgAnti-BCAT2 Antibody Picoband® Western blot analysis of BCAT2 using anti-BCAT2 antibody (A06369-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCAT2 antigen affinity purified polyclonal antibody (Catalog # A06369-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCAT2 at approximately 39 kDa. The expected band size for BCAT2 is at 44, 38-42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-wb-testing-2.jpgAnti-BCAT2 Antibody Picoband® Western blot analysis of BCAT2 using anti-BCAT2 antibody (A06369-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: rat heart tissue lysates, Lane 3: rat stomach tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCAT2 antigen affinity purified polyclonal antibody (Catalog # A06369-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCAT2 at approximately 39 kDa. The expected band size for BCAT2 is at 44, 38-42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-ihc-testing-3.jpgAnti-BCAT2 Antibody Picoband® IHC analysis of BCAT2 using anti-BCAT2 antibody (A06369-1). BCAT2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCAT2 Antibody (A06369-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-ihc-testing-4.jpgAnti-BCAT2 Antibody Picoband® IHC analysis of BCAT2 using anti-BCAT2 antibody (A06369-1). BCAT2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCAT2 Antibody (A06369-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-ihc-testing-5.jpgAnti-BCAT2 Antibody Picoband® IHC analysis of BCAT2 using anti-BCAT2 antibody (A06369-1). BCAT2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCAT2 Antibody (A06369-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-ihc-testing-6.jpgAnti-BCAT2 Antibody Picoband® IHC analysis of BCAT2 using anti-BCAT2 antibody (A06369-1). BCAT2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCAT2 Antibody (A06369-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-if-testing-7.jpgAnti-BCAT2 Antibody Picoband® IF analysis of BCAT2 using anti-BCAT2 antibody (A06369-1). BCAT2 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-BCAT2 Antibody (A06369-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06369-1-bcat2-primary-antibodies-fcm-testing-8.pngAnti-BCAT2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-BCAT2 antibody (A06369-1). Overlay histogram showing MCF-7 cells stained with A06369-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BCAT2 Antibody (A06369-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdhb14-picoband-trade-antibody-a13272-1-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13272-1-pcdhb14-primary-antibodies-wb-testing-1.jpgAnti-PCDHB14 Antibody Picoband® Western blot analysis of PCDHB14 using anti-PCDHB14 antibody (A13272-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse ANA-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHB14 antigen affinity purified polyclonal antibody (Catalog # A13272-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHB14 at approximately 95 kDa. The expected band size for PCDHB14 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13272-1-pcdhb14-primary-antibodies-ihc-testing-2.jpgAnti-PCDHB14 Antibody Picoband® IHC analysis of PCDHB14 using anti-PCDHB14 antibody (A13272-1). PCDHB14 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCDHB14 Antibody (A13272-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13272-1-pcdhb14-primary-antibodies-ihc-testing-3.jpgAnti-PCDHB14 Antibody Picoband® IHC analysis of PCDHB14 using anti-PCDHB14 antibody (A13272-1). PCDHB14 was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCDHB14 Antibody (A13272-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13272-1-pcdhb14-primary-antibodies-ihc-testing-4.jpgAnti-PCDHB14 Antibody Picoband® IHC analysis of PCDHB14 using anti-PCDHB14 antibody (A13272-1). PCDHB14 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCDHB14 Antibody (A13272-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13272-1-pcdhb14-primary-antibodies-fcm-testing-5.pngAnti-PCDHB14 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PCDHB14 antibody (A13272-1). Overlay histogram showing SH-SY5Y cells stained with A13272-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHB14 Antibody (A13272-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdhga2-picoband-trade-antibody-a17592-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17592-pcdhga2-primary-antibodies-wb-testing-1.jpgAnti-PCDHGA2 Antibody Picoband® Western blot analysis of PCDHGA2 using anti-PCDHGA2 antibody (A17592). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHGA2 antigen affinity purified polyclonal antibody (Catalog # A17592) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHGA2 at approximately 90 kDa. The expected band size for PCDHGA2 is at 90,101 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-pdf-picoband-trade-antibody-a00304-1-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-wb-testing-1.jpgAnti-PDF Antibody Picoband® Western blot analysis of PDF using anti-PDF antibody (A00304-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDF antigen affinity purified polyclonal antibody (Catalog # A00304-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDF at approximately 25 kDa. The expected band size for PDF is at 27,60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-wb-testing-2.jpgAnti-PDF Antibody Picoband® Western blot analysis of PDF using anti-PDF antibody (A00304-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDF antigen affinity purified polyclonal antibody (Catalog # A00304-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDF at approximately 25 kDa. The expected band size for PDF is at 27,60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-ihc-testing-3.jpgAnti-PDF Antibody Picoband® IHC analysis of PDF using anti-PDF antibody (A00304-1). PDF was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDF Antibody (A00304-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-ihc-testing-4.jpgAnti-PDF Antibody Picoband® IHC analysis of PDF using anti-PDF antibody (A00304-1). PDF was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDF Antibody (A00304-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-ihc-testing-5.jpgAnti-PDF Antibody Picoband® IHC analysis of PDF using anti-PDF antibody (A00304-1). PDF was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDF Antibody (A00304-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-ihc-testing-6.jpgAnti-PDF Antibody Picoband® IHC analysis of PDF using anti-PDF antibody (A00304-1). PDF was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDF Antibody (A00304-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-ihc-testing-7.jpgAnti-PDF Antibody Picoband® IHC analysis of PDF using anti-PDF antibody (A00304-1). PDF was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDF Antibody (A00304-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-if-testing-8.jpgAnti-PDF Antibody Picoband® IF analysis of PDF using anti-PDF antibody (A00304-1). PDF was detected in a paraffin-embedded section of human esophageal squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PDF Antibody (A00304-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-if-testing-9.jpgAnti-PDF Antibody Picoband® IF analysis of PDF using anti-PDF antibody (A00304-1). PDF was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PDF Antibody (A00304-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-fcm-testing-10.pngAnti-PDF Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PDF antibody (A00304-1). Overlay histogram showing MCF-7 cells stained with A00304-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDF Antibody (A00304-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00304-1-pdf-primary-antibodies-fcm-testing-11.pngAnti-PDF Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PDF antibody (A00304-1). Overlay histogram showing MCF-7 cells stained with A00304-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDF Antibody (A00304-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcmt1-picoband-trade-antibody-a04579-2-boster.html2026-03-16T09:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-wb-testing-1.jpgAnti-PCMT1 Antibody Picoband® Western blot analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: human K562 whole cell lysates, Lane 6: human MCF-7 whole cell lysates, Lane 7: human Caco-2 whole cell lysates, Lane 8: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCMT1 antigen affinity purified polyclonal antibody (Catalog # A04579-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCMT1 at approximately 25 kDa. The expected band size for PCMT1 is at 25, 25-28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-wb-testing-2.jpgAnti-PCMT1 Antibody Picoband® Western blot analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: rat brain tissue lysates, Lane 3: rat liver tissue lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCMT1 antigen affinity purified polyclonal antibody (Catalog # A04579-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCMT1 at approximately 25 kDa. The expected band size for PCMT1 is at 25, 25-28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-ihc-testing-3.jpgAnti-PCMT1 Antibody Picoband® IHC analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). PCMT1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCMT1 Antibody (A04579-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-ihc-testing-4.jpgAnti-PCMT1 Antibody Picoband® IHC analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). PCMT1 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCMT1 Antibody (A04579-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-ihc-testing-5.jpgAnti-PCMT1 Antibody Picoband® IHC analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). PCMT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCMT1 Antibody (A04579-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-ihc-testing-6.jpgAnti-PCMT1 Antibody Picoband® IHC analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). PCMT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCMT1 Antibody (A04579-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-ihc-testing-7.jpgAnti-PCMT1 Antibody Picoband® IHC analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). PCMT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCMT1 Antibody (A04579-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-if-testing-8.jpgAnti-PCMT1 Antibody Picoband® IF analysis of PCMT1 using anti-PCMT1 antibody (A04579-2). PCMT1 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PCMT1 Antibody (A04579-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-fcm-testing-9.pngAnti-PCMT1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PCMT1 antibody (A04579-2). Overlay histogram showing HepG2 cells stained with A04579-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PCMT1 Antibody (A04579-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04579-2-pcmt1-primary-antibodies-fcm-testing-10.pngAnti-PCMT1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-PCMT1 antibody (A04579-2). Overlay histogram showing K562 cells stained with A04579-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PCMT1 Antibody (A04579-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcolce-picoband-trade-antibody-a06428-2-boster.html2026-03-16T09:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06428-2-pcolce-primary-antibodies-wb-testing-1.jpgAnti-PCOLCE Antibody Picoband® Western blot analysis of PCOLCE using anti-PCOLCE antibody (A06428-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCOLCE antigen affinity purified polyclonal antibody (Catalog # A06428-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCOLCE at approximately 50 kDa. The expected band size for PCOLCE is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06428-2-pcolce-primary-antibodies-ihc-testing-2.jpgAnti-PCOLCE Antibody Picoband® IHC analysis of PCOLCE using anti-PCOLCE antibody (A06428-2). PCOLCE was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCOLCE Antibody (A06428-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06428-2-pcolce-primary-antibodies-ihc-testing-3.jpgAnti-PCOLCE Antibody Picoband® IHC analysis of PCOLCE using anti-PCOLCE antibody (A06428-2). PCOLCE was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCOLCE Antibody (A06428-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06428-2-pcolce-primary-antibodies-fcm-testing-4.pngAnti-PCOLCE Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PCOLCE antibody (A06428-2). Overlay histogram showing SH-SY5Y cells stained with A06428-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCOLCE Antibody (A06428-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-eif3b-picoband-trade-antibody-a04318-1-boster.html2026-03-16T09:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-wb-testing-1.jpgAnti-EIF3B Antibody Picoband® Western blot analysis of EIF3B using anti-EIF3B antibody (A04318-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: human MCF-7 whole cell lysates, Lane 6: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF3B antigen affinity purified polyclonal antibody (Catalog # A04318-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EIF3B at approximately 115 kDa. The expected band size for EIF3B is at 92, 115 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-ihc-testing-2.jpgAnti-EIF3B Antibody Picoband® IHC analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-ihc-testing-3.jpgAnti-EIF3B Antibody Picoband® IHC analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-ihc-testing-4.jpgAnti-EIF3B Antibody Picoband® IHC analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-ihc-testing-5.jpgAnti-EIF3B Antibody Picoband® IHC analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-ihc-testing-6.jpgAnti-EIF3B Antibody Picoband® IHC analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-ihc-testing-7.jpgAnti-EIF3B Antibody Picoband® IHC analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-ihc-testing-8.jpgAnti-EIF3B Antibody Picoband® IHC analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-if-testing-9.jpgAnti-EIF3B Antibody Picoband® IF analysis of EIF3B using anti-EIF3B antibody (A04318-1). EIF3B was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-EIF3B Antibody (A04318-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04318-1-eif3b-primary-antibodies-fcm-testing-10.pngAnti-EIF3B Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-EIF3B antibody (A04318-1). Overlay histogram showing Caco-2 cells stained with A04318-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EIF3B Antibody (A04318-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-xdh-picoband-trade-antibody-a01884-2-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-2-xdh-primary-antibodies-wb-testing-1.jpgAnti-XDH Antibody Picoband® Western blot analysis of XDH using anti-XDH antibody (A01884-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates, Lane 3: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-XDH antigen affinity purified polyclonal antibody (Catalog # A01884-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for XDH at approximately 150 kDa. The expected band size for XDH is at 146, 147-150 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-2-xdh-primary-antibodies-ihc-testing-2.jpgAnti-XDH Antibody Picoband® IHC analysis of XDH using anti-XDH antibody (A01884-2). XDH was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-XDH Antibody (A01884-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-2-xdh-primary-antibodies-ihc-testing-3.jpgAnti-XDH Antibody Picoband® IHC analysis of XDH using anti-XDH antibody (A01884-2). XDH was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-XDH Antibody (A01884-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-2-xdh-primary-antibodies-ihc-testing-4.jpgAnti-XDH Antibody Picoband® IHC analysis of XDH using anti-XDH antibody (A01884-2). XDH was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-XDH Antibody (A01884-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-2-xdh-primary-antibodies-ihc-testing-5.jpgAnti-XDH Antibody Picoband® IHC analysis of XDH using anti-XDH antibody (A01884-2). XDH was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-XDH Antibody (A01884-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01884-2-xdh-primary-antibodies-fcm-testing-6.pngAnti-XDH Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-XDH antibody (A01884-2). Overlay histogram showing RT4 cells stained with A01884-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-XDH Antibody (A01884-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdhgc3-picoband-trade-antibody-a12828-1-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12828-1-pcdhgc3-primary-antibodies-wb-testing-1.jpgAnti-PCDHGC3 Antibody Picoband® Western blot analysis of PCDHGC3 using anti-PCDHGC3 antibody (A12828-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHGC3 antigen affinity purified polyclonal antibody (Catalog # A12828-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHGC3 at approximately 118 kDa. The expected band size for PCDHGC3 is at 101,118-137 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12828-1-pcdhgc3-primary-antibodies-fcm-testing-2.pngAnti-PCDHGC3 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PCDHGC3 antibody (A12828-1). Overlay histogram showing JK cells stained with A12828-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHGC3 Antibody (A12828-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdhgc4-picoband-trade-antibody-a17271-1-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17271-1-pcdhgc4-primary-antibodies-wb-testing-1.jpgAnti-PCDHGC4 Antibody Picoband® Western blot analysis of PCDHGC4 using anti-PCDHGC4 antibody (A17271-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHGC4 antigen affinity purified polyclonal antibody (Catalog # A17271-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHGC4 at approximately 101 kDa. The expected band size for PCDHGC4 is at 101 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17271-1-pcdhgc4-primary-antibodies-if-testing-2.jpgAnti-PCDHGC4 Antibody Picoband® IF analysis of PCDHGC4 using anti-PCDHGC4 antibody (A17271-1). PCDHGC4 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PCDHGC4 Antibody (A17271-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17271-1-pcdhgc4-primary-antibodies-fcm-testing-3.pngAnti-PCDHGC4 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PCDHGC4 antibody (A17271-1). Overlay histogram showing 293T cells stained with A17271-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHGC4 Antibody (A17271-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pde12-picoband-trade-antibody-a10688-1-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10688-1-pde12-primary-antibodies-wb-testing-1.jpgAnti-PDE12 Antibody Picoband® Western blot analysis of PDE12 using anti-PDE12 antibody (A10688-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: human Caco-2 whole cell lysates, Lane 6: human HepG2 whole cell lysates, Lane 7: human Hela whole cell lysates, Lane 8: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDE12 antigen affinity purified polyclonal antibody (Catalog # A10688-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDE12 at approximately 70 kDa. The expected band size for PDE12 is at 67,65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10688-1-pde12-primary-antibodies-wb-testing-2.jpgAnti-PDE12 Antibody Picoband® Western blot analysis of PDE12 using anti-PDE12 antibody (A10688-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat thymus tissue lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse thymus tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDE12 antigen affinity purified polyclonal antibody (Catalog # A10688-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDE12 at approximately 70 kDa. The expected band size for PDE12 is at 67,65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10688-1-pde12-primary-antibodies-fcm-testing-3.pngAnti-PDE12 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-PDE12 antibody (A10688-1). Overlay histogram showing Caco-2 cells stained with A10688-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDE12 Antibody (A10688-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pdxk-picoband-trade-antibody-a06683-1-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-wb-testing-1.jpgAnti-PDXK Antibody Picoband® Western blot analysis of PDXK using anti-PDXK antibody (A06683-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDXK antigen affinity purified polyclonal antibody (Catalog # A06683-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDXK at approximately 35 kDa. The expected band size for PDXK is at 35,40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-wb-testing-2.jpgAnti-PDXK Antibody Picoband® Western blot analysis of PDXK using anti-PDXK antibody (A06683-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse testis tissue lysates, Lane 3: mouse kidney tissue lysates, Lane 4: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDXK antigen affinity purified polyclonal antibody (Catalog # A06683-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDXK at approximately 35 kDa. The expected band size for PDXK is at 35,40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-wb-testing-3.jpgAnti-PDXK Antibody Picoband® Western blot analysis of PDXK using anti-PDXK antibody (A06683-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human SiHa whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates, After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDXK antigen affinity purified polyclonal antibody (Catalog # A06683-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a DyLight®488 Conjugated Goat Anti-Rabbit IgG (Catalog # BA1127) secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDXK at approximately 35 kDa. The expected band size for PDXK is at 35,40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-ihc-testing-4.jpgAnti-PDXK Antibody Picoband® IHC analysis of PDXK using anti-PDXK antibody (A06683-1). PDXK was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDXK Antibody (A06683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-ihc-testing-5.jpgAnti-PDXK Antibody Picoband® IHC analysis of PDXK using anti-PDXK antibody (A06683-1). PDXK was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDXK Antibody (A06683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-ihc-testing-6.jpgAnti-PDXK Antibody Picoband® IHC analysis of PDXK using anti-PDXK antibody (A06683-1). PDXK was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDXK Antibody (A06683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-ihc-testing-7.jpgAnti-PDXK Antibody Picoband® IHC analysis of PDXK using anti-PDXK antibody (A06683-1). PDXK was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDXK Antibody (A06683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-ihc-testing-8.jpgAnti-PDXK Antibody Picoband® IHC analysis of PDXK using anti-PDXK antibody (A06683-1). PDXK was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PDXK Antibody (A06683-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06683-1-pdxk-primary-antibodies-fcm-testing-9.pngAnti-PDXK Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PDXK antibody (A06683-1). Overlay histogram showing RT4 cells stained with A06683-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDXK Antibody (A06683-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-peg3-picoband-trade-antibody-a02541-2-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02541-2-peg3-primary-antibodies-wb-testing-1.jpgAnti-PEG3 Antibody Picoband® Western blot analysis of PEG3 using anti-PEG3 antibody (A02541-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PEG3 antigen affinity purified polyclonal antibody (Catalog # A02541-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PEG3 at approximately 200 kDa. The expected band size for PEG3 is at 181 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02541-2-peg3-primary-antibodies-if-testing-2.jpgAnti-PEG3 Antibody Picoband® IF analysis of PEG3 using anti-PEG3 antibody (A02541-2). PEG3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PEG3 Antibody (A02541-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02541-2-peg3-primary-antibodies-fcm-testing-3.pngAnti-PEG3 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-PEG3 antibody (A02541-2). Overlay histogram showing PC-3 cells stained with A02541-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PEG3 Antibody (A02541-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pfkp-picoband-trade-antibody-a07337-3-boster.html2026-03-17T05:15:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-3-pfkp-primary-antibodies-wb-testing-1.jpgAnti-PFKP Antibody Picoband® Western blot analysis of PFKP using anti-PFKP antibody (A07337-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PFKP antigen affinity purified polyclonal antibody (Catalog # A07337-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PFKP at approximately 86 kDa. The expected band size for PFKP is at 86, 80-86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-3-pfkp-primary-antibodies-ihc-testing-2.jpgAnti-PFKP Antibody Picoband® IHC analysis of PFKP using anti-PFKP antibody (A07337-3). PFKP was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKP Antibody (A07337-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-3-pfkp-primary-antibodies-ihc-testing-3.jpgAnti-PFKP Antibody Picoband® IHC analysis of PFKP using anti-PFKP antibody (A07337-3). PFKP was detected in a paraffin-embedded section of human diffuse large B cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKP Antibody (A07337-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-3-pfkp-primary-antibodies-ihc-testing-4.jpgAnti-PFKP Antibody Picoband® IHC analysis of PFKP using anti-PFKP antibody (A07337-3). PFKP was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKP Antibody (A07337-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-3-pfkp-primary-antibodies-ihc-testing-5.jpgAnti-PFKP Antibody Picoband® IHC analysis of PFKP using anti-PFKP antibody (A07337-3). PFKP was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKP Antibody (A07337-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-3-pfkp-primary-antibodies-ihc-testing-6.jpgAnti-PFKP Antibody Picoband® IHC analysis of PFKP using anti-PFKP antibody (A07337-3). PFKP was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKP Antibody (A07337-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07337-3-pfkp-primary-antibodies-fcm-testing-7.pngAnti-PFKP Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PFKP antibody (A07337-3). Overlay histogram showing MCF-7 cells stained with A07337-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PFKP Antibody (A07337-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pgap1-picoband-trade-antibody-a08640-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08640-pgap1-primary-antibodies-wb-testing-1.jpgAnti-PGAP1 Antibody Picoband® Western blot analysis of PGAP1 using anti-PGAP1 antibody (A08640). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGAP1 antigen affinity purified polyclonal antibody (Catalog # A08640) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGAP1 at approximately 100,58 kDa. The expected band size for PGAP1 is at 105,49-53,85-90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08640-pgap1-primary-antibodies-fcm-testing-2.pngAnti-PGAP1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PGAP1 antibody (A08640). Overlay histogram showing 293T cells stained with A08640 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PGAP1 Antibody (A08640, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pgc-picoband-trade-antibody-a00218-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00218-1-pgc-primary-antibodies-wb-testing-1.jpgAnti-PGC Antibody Picoband® Western blot analysis of PGC using anti-PGC antibody (A00218-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat stomach tissue lysates, Lane 2: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGC antigen affinity purified polyclonal antibody (Catalog # A00218-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGC at approximately 38 kDa. The expected band size for PGC is at 42,32,38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00218-1-pgc-primary-antibodies-ihc-testing-2.jpgAnti-PGC Antibody Picoband® IHC analysis of PGC using anti-PGC antibody (A00218-1). PGC was detected in a paraffin-embedded section of human gastric adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PGC Antibody (A00218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00218-1-pgc-primary-antibodies-ihc-testing-3.jpgAnti-PGC Antibody Picoband® IHC analysis of PGC using anti-PGC antibody (A00218-1). PGC was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PGC Antibody (A00218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00218-1-pgc-primary-antibodies-ihc-testing-4.jpgAnti-PGC Antibody Picoband® IHC analysis of PGC using anti-PGC antibody (A00218-1). PGC was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PGC Antibody (A00218-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00218-1-pgc-primary-antibodies-if-testing-5.jpgAnti-PGC Antibody Picoband® IF analysis of PGC using anti-PGC antibody (A00218-1). PGC was detected in a paraffin-embedded section of human gastric cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PGC Antibody (A00218-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00218-1-pgc-primary-antibodies-if-testing-6.jpgAnti-PGC Antibody Picoband® IF analysis of PGC using anti-PGC antibody (A00218-1). PGC was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PGC Antibody (A00218-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00218-1-pgc-primary-antibodies-fcm-testing-8.pngAnti-PGC Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PGC antibody (A00218-1). Overlay histogram showing HepG2 cells stained with A00218-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PGC Antibody (A00218-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pgls-picoband-trade-antibody-a02553-2-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02553-2-pgls-primary-antibodies-wb-testing-1.jpgAnti-PGLS Antibody Picoband® Western blot analysis of PGLS using anti-PGLS antibody (A02553-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Ramos whole cell lysates, Lane 3: human CCRF-CEM whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGLS antigen affinity purified polyclonal antibody (Catalog # A02553-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGLS at approximately 28 kDa. The expected band size for PGLS is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02553-2-pgls-primary-antibodies-if-testing-2.jpgAnti-PGLS Antibody Picoband® IF analysis of PGLS using anti-PGLS antibody (A02553-2) and anti-Beta Tubulin antibody (M01857-3). PGLS was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PGLS Antibody (A02553-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02553-2-pgls-primary-antibodies-fcm-testing-3.pngAnti-PGLS Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PGLS antibody (A02553-2). Overlay histogram showing JK cells stained with A02553-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PGLS Antibody (A02553-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pgm3-picoband-trade-antibody-a02052-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02052-1-pgm3-primary-antibodies-wb-testing-1.jpgAnti-PGM3 Antibody Picoband® Western blot analysis of PGM3 using anti-PGM3 antibody (A02052-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human k562 whole cell lysates, Lane 5: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGM3 antigen affinity purified polyclonal antibody (Catalog # A02052-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGM3 at approximately 63 kDa. The expected band size for PGM3 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02052-1-pgm3-primary-antibodies-ihc-testing-2.jpgAnti-PGM3 Antibody Picoband® IHC analysis of PGM3 using anti-PGM3 antibody (A02052-1). PGM3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PGM3 Antibody (A02052-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02052-1-pgm3-primary-antibodies-ihc-testing-3.jpgAnti-PGM3 Antibody Picoband® IHC analysis of PGM3 using anti-PGM3 antibody (A02052-1). PGM3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PGM3 Antibody (A02052-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02052-1-pgm3-primary-antibodies-if-testing-4.jpgAnti-PGM3 Antibody Picoband® IF analysis of PGM3 using anti-PGM3 antibody (A02052-1) and anti-Beta Tubulin antibody (M01857-3). PGM3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PGM3 Antibody (A02052-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02052-1-pgm3-primary-antibodies-if-testing-5.jpgAnti-PGM3 Antibody Picoband® IF analysis of PGM3 using anti-PGM3 antibody (A02052-1). PGM3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PGM3 Antibody (A02052-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02052-1-pgm3-primary-antibodies-fcm-testing-6.pngAnti-PGM3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PGM3 antibody (A02052-1). Overlay histogram showing HepG2 cells stained with A02052-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PGM3 Antibody (A02052-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pgm5-picoband-trade-antibody-a11631-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11631-1-pgm5-primary-antibodies-wb-testing-1.jpgAnti-PGM5 Antibody Picoband® Western blot analysis of PGM5 using anti-PGM5 antibody (A11631-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGM5 antigen affinity purified polyclonal antibody (Catalog # A11631-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGM5 at approximately 62 kDa. The expected band size for PGM5 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11631-1-pgm5-primary-antibodies-fcm-testing-2.pngAnti-PGM5 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PGM5 antibody (A11631-1). Overlay histogram showing MCF-7 cells stained with A11631-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PGM5 Antibody (A11631-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-phc1-picoband-trade-antibody-a06437-3-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06437-3-phc1-primary-antibodies-wb-testing-1.jpgAnti-PHC1 Antibody Picoband® Western blot analysis of PHC1 using anti-PHC1 antibody (A06437-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U2OS whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHC1 antigen affinity purified polyclonal antibody (Catalog # A06437-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHC1 at approximately 140 kDa. The expected band size for PHC1 is at 106,130 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06437-3-phc1-primary-antibodies-if-testing-2.jpgAnti-PHC1 Antibody Picoband® IF analysis of PHC1 using anti-PHC1 antibody (A06437-3). PHC1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PHC1 Antibody (A06437-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-phf6-picoband-trade-antibody-a03065-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-wb-testing-1.jpgAnti-PHF6 Antibody Picoband® Western blot analysis of PHF6 using anti-PHF6 antibody (A03065-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF6 antigen affinity purified polyclonal antibody (Catalog # A03065-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHF6 at approximately 41 kDa. The expected band size for PHF6 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-2.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-3.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-4.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-5.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-6.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-7.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-8.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-9.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-10.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-11.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-12.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-13.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-ihc-testing-14.jpgAnti-PHF6 Antibody Picoband® IHC analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-if-testing-15.jpgAnti-PHF6 Antibody Picoband® IF analysis of PHF6 using anti-PHF6 antibody (A03065-1). PHF6 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PHF6 Antibody (A03065-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03065-1-phf6-primary-antibodies-fcm-testing-16.pngAnti-PHF6 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PHF6 antibody (A03065-1). Overlay histogram showing JK cells stained with A03065-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHF6 Antibody (A03065-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-phf11-picoband-trade-antibody-a09621-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09621-1-phf11-primary-antibodies-wb-testing-1.jpgAnti-PHF11 Antibody Picoband® Western blot analysis of PHF11 using anti-PHF11 antibody (A09621-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF11 antigen affinity purified polyclonal antibody (Catalog # A09621-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHF11 at approximately 34 kDa. The expected band size for PHF11 is at 38,34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09621-1-phf11-primary-antibodies-if-testing-2.jpgAnti-PHF11 Antibody Picoband® IF analysis of PHF11 using anti-PHF11 antibody (A09621-1). PHF11 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PHF11 Antibody (A09621-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09621-1-phf11-primary-antibodies-fcm-testing-3.pngAnti-PHF11 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PHF11 antibody (A09621-1). Overlay histogram showing 293T cells stained with A09621-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHF11 Antibody (A09621-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09621-1-phf11-primary-antibodies-fcm-testing-4.pngAnti-PHF11 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PHF11 antibody (A09621-1). Overlay histogram showing Hela cells stained with A09621-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHF11 Antibody (A09621-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pi4k2b-picoband-trade-antibody-a11023-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11023-1-pi4k2b-primary-antibodies-wb-testing-1.jpgAnti-PI4K2B Antibody Picoband® Western blot analysis of PI4K2B using anti-PI4K2B antibody (A11023-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PI4K2B antigen affinity purified polyclonal antibody (Catalog # A11023-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PI4K2B at approximately 50 kDa. The expected band size for PI4K2B is at 55,50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11023-1-pi4k2b-primary-antibodies-if-testing-2.jpgAnti-PI4K2B Antibody Picoband® IF analysis of PI4K2B using anti-PI4K2B antibody (A11023-1). PI4K2B was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PI4K2B Antibody (A11023-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11023-1-pi4k2b-primary-antibodies-fcm-testing-3.pngAnti-PI4K2B Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PI4K2B antibody (A11023-1). Overlay histogram showing MCF-7 cells stained with A11023-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PI4K2B Antibody (A11023-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pi4kb-picoband-trade-antibody-a04249-2-boster.html2026-03-16T09:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04249-2-pi4kb-primary-antibodies-wb-testing-1.jpgAnti-PI4KB Antibody Picoband® Western blot analysis of PI4KB using anti-PI4KB antibody (A04249-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PI4KB antigen affinity purified polyclonal antibody (Catalog # A04249-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PI4KB at approximately 95 kDa. The expected band size for PI4KB is at 91,91-110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04249-2-pi4kb-primary-antibodies-ihc-testing-2.jpgAnti-PI4KB Antibody Picoband® IHC analysis of PI4KB using anti-PI4KB antibody (A04249-2). PI4KB was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PI4KB Antibody (A04249-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04249-2-pi4kb-primary-antibodies-fcm-testing-3.pngAnti-PI4KB Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PI4KB antibody (A04249-2). Overlay histogram showing JK cells stained with A04249-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PI4KB Antibody (A04249-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04249-2-pi4kb-primary-antibodies-fcm-testing-4.pngAnti-PI4KB Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-PI4KB antibody (A04249-2). Overlay histogram showing U251 cells stained with A04249-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PI4KB Antibody (A04249-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pik3ap1-picoband-trade-antibody-a08114-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08114-pik3ap1-primary-antibodies-wb-testing-1.jpgAnti-PIK3AP1 Antibody Picoband® Western blot analysis of PIK3AP1 using anti-PIK3AP1 antibody (A08114). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIK3AP1 antigen affinity purified polyclonal antibody (Catalog # A08114) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIK3AP1 at approximately 90 kDa. The expected band size for PIK3AP1 is at 90,95,100 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-pik3r4-picoband-trade-antibody-a06618-1-boster.html2026-03-16T09:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06618-1-pik3r4-primary-antibodies-wb-testing-1.jpgAnti-PIK3R4 Antibody Picoband® Western blot analysis of VPS15/PIK3R4 using anti-VPS15/PIK3R4 antibody (A06618-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VPS15/PIK3R4 antigen affinity purified polyclonal antibody (Catalog # A06618-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VPS15/PIK3R4 at approximately 150 kDa. The expected band size for VPS15/PIK3R4 is at 153 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06618-1-pik3r4-primary-antibodies-fcm-testing-2.pngAnti-PIK3R4 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-VPS15/PIK3R4 antibody (A06618-1). Overlay histogram showing HepG2 cells stained with A06618-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-VPS15/PIK3R4 Antibody (A06618-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pik3r5-picoband-trade-antibody-a02827-2-boster.html2026-03-16T09:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02827-2-pik3r5-primary-antibodies-wb-testing-1.jpgAnti-PIK3R5 Antibody Picoband® Western blot analysis of PIK3R5 using anti-PIK3R5 antibody (A02827-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse Neuro-2a whole cell tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIK3R5 antigen affinity purified polyclonal antibody (Catalog # A02827-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIK3R5 at approximately 97 kDa. The expected band size for PIK3R5 is at 97,55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02827-2-pik3r5-primary-antibodies-fcm-testing-2.pngAnti-PIK3R5 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PIK3R5 antibody (A02827-2). Overlay histogram showing JK cells stained with A02827-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PIK3R5 Antibody (A02827-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pir-picoband-trade-antibody-a03468-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03468-1-pir-primary-antibodies-wb-testing-1.jpgAnti-PIR Antibody Picoband® Western blot analysis of PIR using anti-PIR antibody (A03468-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: monkey COS-7 whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat RH-35 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIR antigen affinity purified polyclonal antibody (Catalog # A03468-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIR at approximately 95 kDa. The expected band size for PIR is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03468-1-pir-primary-antibodies-if-testing-2.jpgAnti-PIR Antibody Picoband® IF analysis of PIR using anti-PIR antibody (A03468-1). PIR was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PIR Antibody (A03468-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03468-1-pir-primary-antibodies-fcm-testing-3.pngAnti-PIR Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PIR antibody (A03468-1). Overlay histogram showing HepG2 cells stained with A03468-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PIR Antibody (A03468-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-sgk493-pkdcc-picoband-trade-antibody-a11391-1-boster.html2026-03-16T09:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-wb-testing-1.jpgAnti-SGK493/PKDCC Antibody Picoband® Western blot analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SGK493/PKDCC antigen affinity purified polyclonal antibody (Catalog # A11391-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SGK493/PKDCC at approximately 54 kDa. The expected band size for SGK493/PKDCC is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-ihc-testing-2.jpgAnti-SGK493/PKDCC Antibody Picoband® IHC analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-ihc-testing-3.jpgAnti-SGK493/PKDCC Antibody Picoband® IHC analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-ihc-testing-4.jpgAnti-SGK493/PKDCC Antibody Picoband® IHC analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-ihc-testing-5.jpgAnti-SGK493/PKDCC Antibody Picoband® IHC analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human mucinous adenoma of ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-ihc-testing-6.jpgAnti-SGK493/PKDCC Antibody Picoband® IHC analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-ihc-testing-7.jpgAnti-SGK493/PKDCC Antibody Picoband® IHC analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-ihc-testing-8.jpgAnti-SGK493/PKDCC Antibody Picoband® IHC analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-if-testing-9.jpgAnti-SGK493/PKDCC Antibody Picoband® IF analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-if-testing-10.jpgAnti-SGK493/PKDCC Antibody Picoband® IF analysis of SGK493/PKDCC using anti-SGK493/PKDCC antibody (A11391-1). SGK493/PKDCC was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SGK493/PKDCC Antibody (A11391-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11391-1-pkdcc-primary-antibodies-fcm-testing-11.pngAnti-SGK493/PKDCC Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-SGK493/PKDCC antibody (A11391-1). Overlay histogram showing HepG2 cells stained with A11391-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SGK493/PKDCC Antibody (A11391-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lmf2-picoband-trade-antibody-a13780-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13780-1-lmf2-primary-antibodies-wb-testing-1_1.jpgAnti-LMF2 Antibody Picoband® Western blot analysis of LMF2 using anti-LMF2 antibody (A13780-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMF2 antigen affinity purified polyclonal antibody (Catalog # A13780-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LMF2 at approximately 80 kDa. The expected band size for LMF2 is at 80 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-icmt-picoband-trade-antibody-a06174-1-boster.html2026-03-17T05:15:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06174-1-icmt-primary-antibodies-wb-testing-1.jpgAnti-ICMT Antibody Picoband® Western blot analysis of ICMT using anti-ICMT antibody (A06174-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICMT antigen affinity purified polyclonal antibody (Catalog # A06174-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ICMT at approximately 32 kDa. The expected band size for ICMT is at 32 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-htr3c-picoband-trade-antibody-a10495-1-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10495-1-htr3c-primary-antibodies-wb-testing-1.jpgAnti-HTR3C Antibody Picoband® Western blot analysis of HTR3C using anti-HTR3C antibody (A10495-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HTR3C antigen affinity purified polyclonal antibody (Catalog # A10495-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HTR3C at approximately 50 kDa. The expected band size for HTR3C is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10495-1-htr3c-primary-antibodies-if-testing-2.jpgAnti-HTR3C Antibody Picoband® IF analysis of HTR3C using anti-HTR3C antibody (A10495-1). HTR3C was detected in an immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HTR3C Antibody (A10495-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-htra2-picoband-trade-antibody-a01941-3-boster.html2026-03-16T09:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01941-3-htra2-primary-antibodies-wb-testing-1.jpgAnti-HTRA2 Antibody Picoband® Western blot analysis of HTRA2 using anti-HTRA2 antibody (A01941-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HT-1080 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HTRA2 antigen affinity purified polyclonal antibody (Catalog # A01941-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HTRA2 at approximately 36 kDa. The expected band size for HTRA2 is at 36,49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01941-3-htra2-primary-antibodies-ihc-testing-2.jpgAnti-HTRA2 Antibody Picoband® IHC analysis of HTRA2 using anti-HTRA2 antibody (A01941-3). HTRA2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTRA2 Antibody (A01941-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01941-3-htra2-primary-antibodies-ihc-testing-3.jpgAnti-HTRA2 Antibody Picoband® IHC analysis of HTRA2 using anti-HTRA2 antibody (A01941-3). HTRA2 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTRA2 Antibody (A01941-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01941-3-htra2-primary-antibodies-if-testing-4.jpgAnti-HTRA2 Antibody Picoband® IF analysis of HTRA2 using anti-HTRA2 antibody (A01941-3). HTRA2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HTRA2 Antibody (A01941-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01941-3-htra2-primary-antibodies-fcm-testing-5.pngAnti-HTRA2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-HTRA2 antibody (A01941-3). Overlay histogram showing HEL cells stained with A01941-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HTRA2 Antibody (A01941-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-alox12-picoband-trade-antibody-a02275-2-boster.html2026-03-16T09:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02275-2-alox12-primary-antibodies-wb-testing-1_1.jpgAnti-ALOX12 Antibody Picoband®Western blot analysis of ALOX12 using anti-ALOX12 antibody (A02275-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat spleen tissue lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse spleen tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALOX12 antigen affinity purified polyclonal antibody (A02275-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ALOX12 at approximately 76 kDa. The expected band size for ALOX12 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02275-2-alox12-primary-antibodies-if-testing-1.jpgAnti-ALOX12 Antibody Picoband®IF analysis of ALOX12 using anti-ALOX12 antibody (A02275-2). ALOX12 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ALOX12 Antibody (A02275-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-klf4-picoband-trade-antibody-a00120-4-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00120-4-klf4-primary-antibodies-wb-testing-1.jpgAnti-Klf4 Antibody Picoband® Western blot analysis of Klf4 using anti-Klf4 antibody (A00120-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat small intestine tissue lysates, Lane 2: rat lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Klf4 antigen affinity purified polyclonal antibody (Catalog # A00120-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Klf4 at approximately 65 kDa. The expected band size for Klf4 is at 50-65 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-hcn2-picoband-trade-antibody-a02804-1-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-wb-testing-1.jpgAnti-Hcn2 Antibody Picoband® Western blot analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hcn2 antigen affinity purified polyclonal antibody (Catalog # A02804-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hcn2 at approximately 110 kDa. The expected band size for Hcn2 is at 97-110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-ihc-testing-2.jpgAnti-Hcn2 Antibody Picoband® IHC analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Hcn2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hcn2 Antibody (A02804-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-ihc-testing-3.jpgAnti-Hcn2 Antibody Picoband® IHC analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Hcn2 was detected in a paraffin-embedded section of mouse cardiac tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hcn2 Antibody (A02804-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-ihc-testing-4.jpgAnti-Hcn2 Antibody Picoband® IHC analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Hcn2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hcn2 Antibody (A02804-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-ihc-testing-5.jpgAnti-Hcn2 Antibody Picoband® IHC analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Hcn2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hcn2 Antibody (A02804-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-ihc-testing-6.jpgAnti-Hcn2 Antibody Picoband® IHC analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Hcn2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hcn2 Antibody (A02804-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-ihc-testing-7.jpgAnti-Hcn2 Antibody Picoband® IHC analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Hcn2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hcn2 Antibody (A02804-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-ihc-testing-8.jpgAnti-Hcn2 Antibody Picoband® IHC analysis of Hcn2 using anti-Hcn2 antibody (A02804-1). Hcn2 was detected in a paraffin-embedded section of rat cardiac tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Hcn2 Antibody (A02804-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-fcm-testing-9.pngAnti-Hcn2 Antibody Picoband® Flow Cytometry analysis of Neuro-2a cells using anti-Hcn2 antibody (A02804-1). Overlay histogram showing Neuro-2a cells stained with A02804-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Hcn2 Antibody (A02804-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02804-1-hcn2-primary-antibodies-fcm-testing-10.pngAnti-Hcn2 Antibody Picoband® Flow Cytometry analysis of NIH/3T3 cells using anti-Hcn2 antibody (A02804-1). Overlay histogram showing NIH/3T3 cells stained with A02804-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Hcn2 Antibody (A02804-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pkp2-picoband-trade-antibody-a02146-2-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-wb-testing-1.jpgAnti-PKP2 Antibody Picoband® Western blot analysis of PKP2 using anti-PKP2 antibody (A02146-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PKP2 antigen affinity purified polyclonal antibody (Catalog # A02146-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PKP2 at approximately 92 kDa. The expected band size for PKP2 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-ihc-testing-2.jpgAnti-PKP2 Antibody Picoband® IHC analysis of PKP2 using anti-PKP2 antibody (A02146-2). PKP2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PKP2 Antibody (A02146-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-ihc-testing-3.jpgAnti-PKP2 Antibody Picoband® IHC analysis of PKP2 using anti-PKP2 antibody (A02146-2). PKP2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PKP2 Antibody (A02146-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-ihc-testing-4.jpgAnti-PKP2 Antibody Picoband® IHC analysis of PKP2 using anti-PKP2 antibody (A02146-2). PKP2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PKP2 Antibody (A02146-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-ihc-testing-5.jpgAnti-PKP2 Antibody Picoband® IHC analysis of PKP2 using anti-PKP2 antibody (A02146-2). PKP2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PKP2 Antibody (A02146-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-ihc-testing-6.jpgAnti-PKP2 Antibody Picoband® IHC analysis of PKP2 using anti-PKP2 antibody (A02146-2). PKP2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PKP2 Antibody (A02146-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-ihc-testing-7.jpgAnti-PKP2 Antibody Picoband® IHC analysis of PKP2 using anti-PKP2 antibody (A02146-2). PKP2 was detected in a paraffin-embedded section of mouse cardiac tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PKP2 Antibody (A02146-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-if-testing-8.jpgAnti-PKP2 Antibody Picoband® IF analysis of PKP2 using anti-PKP2 antibody (A02146-2) and anti-Beta Tubulin antibody (M01857-3). PKP2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PKP2 Antibody (A02146-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02146-2-pkp2-primary-antibodies-fcm-testing-9.pngAnti-PKP2 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-PKP2 antibody (A02146-2). Overlay histogram showing U87 cells stained with A02146-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PKP2 Antibody (A02146-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nudt15-picoband-trade-antibody-a05498-2-boster.html2026-03-16T09:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05498-2-nudt15-primary-antibodies-wb-testing-1.jpgAnti-NUDT15 Antibody Picoband® Western blot analysis of NUDT15 using anti-NUDT15 antibody (A05498-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT15 antigen affinity purified polyclonal antibody (Catalog # A05498-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDT15 at approximately 19 kDa. The expected band size for NUDT15 is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05498-2-nudt15-primary-antibodies-if-testing-2.jpgAnti-NUDT15 Antibody Picoband® IF analysis of NUDT15 using anti-NUDT15 antibody (A05498-2). NUDT15 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUDT15 Antibody (A05498-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-numbl-picoband-trade-antibody-a07925-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07925-numbl-primary-antibodies-wb-testing-1.jpgAnti-NUMBL Antibody Picoband® Western blot analysis of NUMBL using anti-NUMBL antibody (A07925). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U-87 MG whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUMBL antigen affinity purified polyclonal antibody (Catalog # A07925) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUMBL at approximately 72 kDa. The expected band size for NUMBL is at 65-70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07925-numbl-primary-antibodies-fcm-testing-2.pngAnti-NUMBL Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-NUMBL antibody (A07925). Overlay histogram showing U87 cells stained with A07925 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUMBL Antibody (A07925, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mansc4-picoband-trade-antibody-a19343-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19343-mansc4-primary-antibodies-wb-testing-1.jpgAnti-MANSC4 Antibody Picoband® Western blot analysis of MANSC4 using anti-MANSC4 antibody (A19343). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: monkey COS-7 whole cell lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse kidney tissue lysates. Lane 6: mouse HBZY whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MANSC4 antigen affinity purified polyclonal antibody (Catalog # A19343) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MANSC4 at approximately 45 kDa. The expected band size for MANSC4 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19343-mansc4-primary-antibodies-ihc-testing-2.jpgAnti-MANSC4 Antibody Picoband® IHC analysis of MANSC4 using anti-MANSC4 antibody (A19343). MANSC4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MANSC4 Antibody (A19343) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19343-mansc4-primary-antibodies-ihc-testing-3.jpgAnti-MANSC4 Antibody Picoband® IHC analysis of MANSC4 using anti-MANSC4 antibody (A19343). MANSC4 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MANSC4 Antibody (A19343) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19343-mansc4-primary-antibodies-if-testing-1.jpgAnti-MANSC4 Antibody Picoband®IF analysis of MANSC4 using anti-MANSC4 antibody (A193433). MANSC4 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MANSC4 Antibody (A19343) overnight at 4°C. Cy Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19343-mansc4-primary-antibodies-fcm-testing-4.pngAnti-MANSC4 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-MANSC4 antibody (A19343). Overlay histogram showing Caco-2 cells stained with A19343 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MANSC4 Antibody (A19343, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19343-mansc4-primary-antibodies-fcm-testing-5.pngAnti-MANSC4 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-MANSC4 antibody (A19343). Overlay histogram showing PC-3 cells stained with A19343 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MANSC4 Antibody (A19343, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mfsd12-picoband-trade-antibody-a16855-1-boster.html2026-04-06T05:04:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16855-1-mfsd12-primary-antibodies-wb-testing-1.jpgAnti-MFSD12 Antibody Picoband® Western blot analysis of MFSD12 using anti-MFSD12 antibody (A16855-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MFSD12 antigen affinity purified polyclonal antibody (Catalog # A16855-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MFSD12 at approximately 52 kDa. The expected band size for MFSD12 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16855-1-fimmu-16-1681887-g003.jpgAnti-MFSD12 Antibody Picoband®The protein expression analysis of MFSD12. (A) Pan-cancer protein expression profile of MFSD12 and representative IHC staining of tissue microarrays in HPA database. (B) IHC analysis of MFSD12 in LIHC tumor tissues and paired adjacent non-tumor liver tissues. (C) Quantification of immunostains for MFSD12 by IOD analysis. * P < 0.05, ** P < 0.01. IHC, immunohistochemistry; HPA, Human Protein Atlas; LIHC, liver hepatocellular carcinoma; IOD, integrated optical density;. Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12582970/'>41194934</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16855-1-fimmu-16-1681887-g012.jpgAnti-MFSD12 Antibody Picoband®The knockdown of MFSD12 inhibited the proliferation, migration, and invasion of LIHC cells, as well as the TIM-3/Galectin-9 signaling pathway. (A, B) RT-qPCR and Western blot validation of MFSD12 silencing efficiency using siRNAs (si-MFSD12–1 to −4) with GAPDH as loading control. (C) CCK-8 cell viability assay showing reduced HEP 3B2.1–7 cells proliferation after MFSD12 knockdown (si-MFSD12-3). (D) Transwell assay revealed a reduction in the migratory and invasive capabilities of HEP 3B2.1–7 cells following the knockdown of MFSD12. (E) Immunoblot analysis of EMT markers and TIM-3 axis components showing up-regulation of E-cadherin and down-regulation of Vimentin, MMP-2, MMP-9, HAVCR2 (TIM-3) and LGALS9 in si-MFSD12-treated cells. * P < 0.05, ** P < 0.01, *** P < 0.001. CTRL, control untreated; si-NC, negative control siRNA; si-MFSD12, MFSD12-targeting siRNA; E-cadherin, epithelial cadherin; MMP-2/9, matrix metalloproteinase-2/9; HAVCR2, hepatitis A virus cellular receptor 2 (TIM-3); LGALS9, lectin galactoside-binding soluble 9 (Galectin-9). Index in PubMed under a CC BY license. PMID: <a href='https://pmc.ncbi.nlm.nih.gov/articles/PMC12582970/'>41194934</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16855-1-mfsd12-primary-antibodies-ihc-testing-2.jpgAnti-MFSD12 Antibody Picoband® IHC analysis of MFSD12 using anti-MFSD12 antibody (A16855-1). MFSD12 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MFSD12 Antibody (A16855-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16855-1-mfsd12-primary-antibodies-ihc-testing-3.jpgAnti-MFSD12 Antibody Picoband® IHC analysis of MFSD12 using anti-MFSD12 antibody (A16855-1). MFSD12 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MFSD12 Antibody (A16855-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-calreticulin-calr-picoband-trade-antibody-a00894-2-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-wb-testing-1.jpgAnti-Calreticulin/CALR Antibody Picoband® Western blot analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human COLO 320 whole cell lysates, Lane 2: human HL-60 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human SH-SY5Y whole cell lysates, Lane 6: human THP-1 whole cell lysates, Lane 7: human U251 whole cell lysates, Lane 8: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calreticulin/CALR antigen affinity purified polyclonal antibody (Catalog # A00894-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calreticulin/CALR at approximately 50 kDa. The expected band size for Calreticulin/CALR is at 48, 55-65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-wb-testing-2.jpgAnti-Calreticulin/CALR Antibody Picoband® Western blot analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat skeletal muscle tissue lysates, Lane 3: rat liver tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse skeletal muscle tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calreticulin/CALR antigen affinity purified polyclonal antibody (Catalog # A00894-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calreticulin/CALR at approximately 50 kDa. The expected band size for Calreticulin/CALR is at 48, 55-65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-3.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-4.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-5.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-6.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-7.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-8.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-9.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-10.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-11.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-12.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-13.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-ihc-testing-14.jpgAnti-Calreticulin/CALR Antibody Picoband® IHC analysis of Calreticulin/CALR using anti-Calreticulin/CALR antibody (A00894-2). Calreticulin/CALR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Calreticulin/CALR Antibody (A00894-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-fcm-testing-15.pngAnti-Calreticulin/CALR Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-Calreticulin/CALR antibody (A00894-2). Overlay histogram showing PC-3 cells stained with A00894-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Calreticulin/CALR Antibody (A00894-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00894-2-calr-primary-antibodies-fcm-testing-16.pngAnti-Calreticulin/CALR Antibody Picoband® Flow Cytometry analysis of C6 cells using anti-Calreticulin/CALR antibody (A00894-2). Overlay histogram showing C6 cells stained with A00894-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Calreticulin/CALR Antibody (A00894-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mocs1-picoband-trade-antibody-a07628-2-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-2-mocs1-primary-antibodies-wb-testing-1.jpgAnti-MOCS1 Antibody Picoband® Western blot analysis of MOCS1 using anti-MOCS1 antibody (A07628-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH-35 whole cell lysates, Lane 7: mouse liver whole cell lysates, Lane 8: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOCS1 antigen affinity purified polyclonal antibody (Catalog # A07628-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOCS1 at approximately 72 kDa. The expected band size for MOCS1 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07628-2-mocs1-primary-antibodies-if-testing-2.jpgAnti-MOCS1 Antibody Picoband® IF analysis of MOCS1 using anti-MOCS1 antibody (A07628-2). MOCS1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MOCS1 Antibody (A07628-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-ints12-picoband-trade-antibody-a11402-1-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11402-1-ints12-primary-antibodies-wb-testing-1.jpgAnti-INTS12 Antibody Picoband® Western blot analysis of INTS12 using anti-INTS12 antibody (A11402-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse SP2/0 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INTS12 antigen affinity purified polyclonal antibody (Catalog # A11402-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INTS12 at approximately 68 kDa. The expected band size for INTS12 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11402-1-ints12-primary-antibodies-fcm-testing-2.pngAnti-INTS12 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-INTS12 antibody (A11402-1). Overlay histogram showing MCF-7 cells stained with A11402-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-INTS12 Antibody (A11402-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ints13-picoband-trade-antibody-a32419-2-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32419-2-ints13-primary-antibodies-wb-testing-1.jpgAnti-INTS13 Antibody Picoband® Western blot analysis of INTS13 using anti-INTS13 antibody (A32419-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human A562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INTS13 antigen affinity purified polyclonal antibody (Catalog # A32419-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INTS13 at approximately 85 kDa. The expected band size for INTS13 is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32419-2-ints13-primary-antibodies-if-testing-2.jpgAnti-INTS13 Antibody Picoband® IF analysis of INTS13 using anti-INTS13 antibody (A32419-2) and anti-Beta Tubulin antibody (M01857-3). INTS13 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-INTS13 Antibody (A32419-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-ints14-picoband-trade-antibody-a32420-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32420-ints14-primary-antibodies-wb-testing-1.jpgAnti-INTS14 Antibody Picoband® Western blot analysis of INTS14 using anti-INTS14 antibody (A32420). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INTS14 antigen affinity purified polyclonal antibody (Catalog # A32420) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INTS14 at approximately 68 kDa. The expected band size for INTS14 is at 57 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-intu-picoband-trade-antibody-a11533-1-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11533-1-intu-primary-antibodies-wb-testing-1.jpgAnti-INTU Antibody Picoband® Western blot analysis of INTU using anti-INTU antibody (A11533-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INTU antigen affinity purified polyclonal antibody (Catalog # A11533-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INTU at approximately 100 kDa. The expected band size for INTU is at 80,106 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11533-1-intu-primary-antibodies-ihc-testing-2.jpgAnti-INTU Antibody Picoband® IHC analysis of INTU using anti-INTU antibody (A11533-1). INTU was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INTU Antibody (A11533-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11533-1-intu-primary-antibodies-ihc-testing-3.jpgAnti-INTU Antibody Picoband® IHC analysis of INTU using anti-INTU antibody (A11533-1). INTU was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INTU Antibody (A11533-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11533-1-intu-primary-antibodies-ihc-testing-4.jpgAnti-INTU Antibody Picoband® IHC analysis of INTU using anti-INTU antibody (A11533-1). INTU was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INTU Antibody (A11533-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11533-1-intu-primary-antibodies-if-testing-1.jpgAnti-INTU Antibody Picoband®IF analysis of INTU using anti-INTU antibody (A11533-1). INTU was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-INTU Antibody (A11533-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11533-1-intu-primary-antibodies-fcm-testing-5.pngAnti-INTU Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-INTU antibody (A11533-1). Overlay histogram showing MCF-7 cells stained with A11533-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-INTU Antibody (A11533-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ipo8-picoband-trade-antibody-a07327-2-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07327-2-ipo8-primary-antibodies-wb-testing-1.jpgAnti-IPO8 Antibody Picoband® Western blot analysis of IPO8 using anti-IPO8 antibody (A07327-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IPO8 antigen affinity purified polyclonal antibody (Catalog # A07327-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IPO8 at approximately 120 kDa. The expected band size for IPO8 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07327-2-ipo8-primary-antibodies-ihc-testing-2.jpgAnti-IPO8 Antibody Picoband® IHC analysis of IPO8 using anti-IPO8 antibody (A07327-2). IPO8 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO8 Antibody (A07327-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07327-2-ipo8-primary-antibodies-ihc-testing-3.jpgAnti-IPO8 Antibody Picoband® IHC analysis of IPO8 using anti-IPO8 antibody (A07327-2). IPO8 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO8 Antibody (A07327-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07327-2-ipo8-primary-antibodies-ihc-testing-4.jpgAnti-IPO8 Antibody Picoband® IHC analysis of IPO8 using anti-IPO8 antibody (A07327-2). IPO8 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO8 Antibody (A07327-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-ipo9-picoband-trade-antibody-a10216-2-boster.html2026-03-17T05:15:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-wb-testing-1.jpgAnti-IPO9 Antibody Picoband® Western blot analysis of IPO9 using anti-IPO9 antibody (A10216-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IPO9 antigen affinity purified polyclonal antibody (Catalog # A10216-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IPO9 at approximately 120 kDa. The expected band size for IPO9 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-ihc-testing-2.jpgAnti-IPO9 Antibody Picoband® IHC analysis of IPO9 using anti-IPO9 antibody (A10216-2). IPO9 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO9 Antibody (A10216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-ihc-testing-3.jpgAnti-IPO9 Antibody Picoband® IHC analysis of IPO9 using anti-IPO9 antibody (A10216-2). IPO9 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO9 Antibody (A10216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-ihc-testing-4.jpgAnti-IPO9 Antibody Picoband® IHC analysis of IPO9 using anti-IPO9 antibody (A10216-2). IPO9 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO9 Antibody (A10216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-ihc-testing-5.jpgAnti-IPO9 Antibody Picoband® IHC analysis of IPO9 using anti-IPO9 antibody (A10216-2). IPO9 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO9 Antibody (A10216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-ihc-testing-6.jpgAnti-IPO9 Antibody Picoband® IHC analysis of IPO9 using anti-IPO9 antibody (A10216-2). IPO9 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO9 Antibody (A10216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-ihc-testing-7.jpgAnti-IPO9 Antibody Picoband® IHC analysis of IPO9 using anti-IPO9 antibody (A10216-2). IPO9 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IPO9 Antibody (A10216-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-fcm-testing-8.pngAnti-IPO9 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-IPO9 antibody (A10216-2). Overlay histogram showing Hela cells stained with A10216-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IPO9 Antibody (A10216-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10216-2-ipo9-primary-antibodies-fcm-testing-9.pngAnti-IPO9 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-IPO9 antibody (A10216-2). Overlay histogram showing SH-SY5Y cells stained with A10216-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IPO9 Antibody (A10216-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mum1-irf4-picoband-trade-antibody-a00401-2-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00401-2-irf4-primary-antibodies-wb-testing-1.jpgAnti-MUM1/IRF4 Antibody Picoband® Western blot analysis of MUM1/IRF4 using anti-MUM1/IRF4 antibody (A00401-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hut-78 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MUM1/IRF4 antigen affinity purified polyclonal antibody (Catalog # A00401-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MUM1/IRF4 at approximately 60 kDa. The expected band size for MUM1/IRF4 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00401-2-irf4-primary-antibodies-if-testing-2.jpgAnti-MUM1/IRF4 Antibody Picoband® IF analysis of IRF4 using anti-IRF4 antibody (A00401-2). IRF4 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IRF4 Antibody (A00401-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-irf5-picoband-trade-antibody-a00958-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00958-1-irf5-primary-antibodies-wb-testing-1.jpgAnti-IRF5 Antibody Picoband® Western blot analysis of IRF5 using anti-IRF5 antibody (A00958-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRF5 antigen affinity purified polyclonal antibody (Catalog # A00958-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRF5 at approximately 60 kDa. The expected band size for IRF5 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00958-1-irf5-primary-antibodies-if-testing-2.jpgAnti-IRF5 Antibody Picoband® IF analysis of IRF5 using anti-IRF5 antibody (A00958-1). IRF5 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IRF5 Antibody (A00958-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00958-1-irf5-primary-antibodies-fcm-testing-3.pngAnti-IRF5 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-IRF5 antibody (A00958-1). Overlay histogram showing SH-SY5Y cells stained with A00958-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IRF5 Antibody (A00958-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-isyna1-picoband-trade-antibody-a08693-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-wb-testing-1.jpgAnti-ISYNA1 Antibody Picoband® Western blot analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ISYNA1 antigen affinity purified polyclonal antibody (Catalog # A08693-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ISYNA1 at approximately 61 kDa. The expected band size for ISYNA1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-2.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-3.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-4.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-5.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-6.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-7.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-8.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-9.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08693-1-isyna1-primary-antibodies-ihc-testing-10.jpgAnti-ISYNA1 Antibody Picoband® IHC analysis of ISYNA1 using anti-ISYNA1 antibody (A08693-1). ISYNA1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ISYNA1 Antibody (A08693-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-centromere-protein-r-itgb3bp-picoband-trade-antibody-a09098-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09098-1-itgb3bp-primary-antibodies-wb-testing-1.jpgAnti-Centromere protein R/ITGB3BP Antibody Picoband® Western blot analysis of Centromere protein R/ITGB3BP using anti-Centromere protein R/ITGB3BP antibody (A09098-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Centromere protein R/ITGB3BP antigen affinity purified polyclonal antibody (Catalog # A09098-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Centromere protein R/ITGB3BP at approximately 20 kDa. The expected band size for Centromere protein R/ITGB3BP is at 20,23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09098-1-itgb3bp-primary-antibodies-if-testing-2.jpgAnti-Centromere protein R/ITGB3BP Antibody Picoband® IF analysis of Centromere protein R/ITGB3BP using anti-Centromere protein R/ITGB3BP antibody (A09098-1) and anti-Beta Tubulin antibody (M01857-3). Centromere protein R/ITGB3BP was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Centromere protein R/ITGB3BP Antibody (A09098-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-itpa-picoband-trade-antibody-a02304-boster.html2026-03-16T09:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-wb-testing-1.jpgAnti-ITPA Antibody Picoband® Western blot analysis of ITPA using anti-ITPA antibody (A02304). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITPA antigen affinity purified polyclonal antibody (Catalog # A02304) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITPA at approximately 21 kDa. The expected band size for ITPA is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-2.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-3.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-4.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-5.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-6.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-7.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-8.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-ihc-testing-9.jpgAnti-ITPA Antibody Picoband® IHC analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-if-testing-10.jpgAnti-ITPA Antibody Picoband® IF analysis of ITPA using anti-ITPA antibody (A02304). ITPA was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ITPA Antibody (A02304) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02304-itpa-primary-antibodies-fcm-testing-11.pngAnti-ITPA Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-ITPA antibody (A02304). Overlay histogram showing K562 cells stained with A02304 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ITPA Antibody (A02304, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-itpk1-picoband-trade-antibody-a09106-2-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09106-2-itpk1-primary-antibodies-wb-testing-1.jpgAnti-ITPK1 Antibody Picoband® Western blot analysis of ITPK1 using anti-ITPK1 antibody (A09106-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITPK1 antigen affinity purified polyclonal antibody (Catalog # A09106-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITPK1 at approximately 42 kDa. The expected band size for ITPK1 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09106-2-itpk1-primary-antibodies-fcm-testing-2.pngAnti-ITPK1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-ITPK1 antibody (A09106-2). Overlay histogram showing MCF-7 cells stained with A09106-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ITPK1 Antibody (A09106-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hepacam2-picoband-trade-antibody-a12313-1-boster.html2026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12313-1-hepacam2-primary-antibodies-wb-testing-1.jpgAnti-HEPACAM2 Antibody Picoband® Western blot analysis of HEPACAM2 using anti-HEPACAM2 antibody (A12313-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HEPACAM2 antigen affinity purified polyclonal antibody (Catalog # A12313-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HEPACAM2 at approximately 65 kDa. The expected band size for HEPACAM2 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12313-1-hepacam2-primary-antibodies-ihc-testing-2.jpgAnti-HEPACAM2 Antibody Picoband® IHC analysis of HEPACAM2 using anti-HEPACAM2 antibody (A12313-1). HEPACAM2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HEPACAM2 Antibody (A12313-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12313-1-hepacam2-primary-antibodies-ihc-testing-3.jpgAnti-HEPACAM2 Antibody Picoband® IHC analysis of HEPACAM2 using anti-HEPACAM2 antibody (A12313-1). HEPACAM2 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HEPACAM2 Antibody (A12313-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12313-1-hepacam2-primary-antibodies-ihc-testing-4.jpgAnti-HEPACAM2 Antibody Picoband® IHC analysis of HEPACAM2 using anti-HEPACAM2 antibody (A12313-1). HEPACAM2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HEPACAM2 Antibody (A12313-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-hsd3b7-picoband-trade-antibody-a10025-1-boster.html2026-03-16T09:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10025-1-hsd3b7-primary-antibodies-wb-testing-1.jpgAnti-HSD3B7 Antibody Picoband® Western blot analysis of HSD3B7 using anti-HSD3B7 antibody (A10025-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSD3B7 antigen affinity purified polyclonal antibody (Catalog # A10025-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSD3B7 at approximately 45 kDa. The expected band size for HSD3B7 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10025-1-hsd3b7-primary-antibodies-ihc-testing-1.jpgAnti-HSD3B7 Antibody Picoband®IHC analysis of HSD3B7 using anti-HSD3B7 antibody (A10025-1). HSD3B7 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSD3B7 Antibody (A10025-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10025-1-hsd3b7-primary-antibodies-if-testing-2.jpgAnti-HSD3B7 Antibody Picoband® IF analysis of HSD3B7 using anti-HSD3B7 antibody (A10025-1). HSD3B7 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HSD3B7 Antibody (A10025-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-hsd17b2-picoband-trade-antibody-a02506-1-boster.html2026-03-16T09:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02506-1-hsd17b2-primary-antibodies-wb-testing-1.jpgAnti-HSD17B2 Antibody Picoband® Western blot analysis of HSD17B2 using anti-HSD17B2 antibody (A02506-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human placenta tissue lysates, Lane 5: mouse liver tissue tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSD17B2 antigen affinity purified polyclonal antibody (Catalog # A02506-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSD17B2 at approximately 37 kDa. The expected band size for HSD17B2 is at 43-49,35-40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02506-1-hsd17b2-primary-antibodies-if-testing-2.jpgAnti-HSD17B2 Antibody Picoband® IF analysis of HSD17B2 using anti-HSD17B2 antibody (A02506-1). HSD17B2 was detected in an immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HSD17B2 Antibody (A02506-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02506-1-hsd17b2-primary-antibodies-fcm-testing-3.pngAnti-HSD17B2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-HSD17B2 antibody (A02506-1). Overlay histogram showing MCF-7 cells stained with A02506-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSD17B2 Antibody (A02506-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hsd17b13-picoband-trade-antibody-a12700-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12700-1-hsd17b13-primary-antibodies-wb-testing-1.jpgAnti-HSD17B13 Antibody Picoband® Western blot analysis of HSD17B13 using anti-HSD17B13 antibody (A12700-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 2: rat liver tissue lysates, Lane 3: rat RH-35 whole cell lysates, Lane 4: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSD17B13 antigen affinity purified polyclonal antibody (Catalog # A12700-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSD17B13 at approximately 34 kDa. The expected band size for HSD17B13 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12700-1-hsd17b13-primary-antibodies-ihc-testing-2.jpgAnti-HSD17B13 Antibody Picoband® IHC analysis of HSD17B13 using anti-HSD17B13 antibody (A12700-1). HSD17B13 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSD17B13 Antibody (A12700-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12700-1-hsd17b13-primary-antibodies-ihc-testing-3.jpgAnti-HSD17B13 Antibody Picoband® IHC analysis of HSD17B13 using anti-HSD17B13 antibody (A12700-1). HSD17B13 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSD17B13 Antibody (A12700-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12700-1-hsd17b13-primary-antibodies-ihc-testing-4.jpgAnti-HSD17B13 Antibody Picoband® IHC analysis of HSD17B13 using anti-HSD17B13 antibody (A12700-1). HSD17B13 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSD17B13 Antibody (A12700-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12700-1-hsd17b13-primary-antibodies-fcm-testing-5.pngAnti-HSD17B13 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-HSD17B13 antibody (A12700-1). Overlay histogram showing HepG2 cells stained with A12700-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSD17B13 Antibody (A12700-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hsdl2-picoband-trade-antibody-a11317-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-wb-testing-1.jpgAnti-HSDL2 Antibody Picoband® Western blot analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSDL2 antigen affinity purified polyclonal antibody (Catalog # A11317-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSDL2 at approximately 45 kDa. The expected band size for HSDL2 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-2.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-3.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-4.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-5.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-6.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-7.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-8.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-ihc-testing-9.jpgAnti-HSDL2 Antibody Picoband® IHC analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-if-testing-10.jpgAnti-HSDL2 Antibody Picoband® IF analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-if-testing-11.jpgAnti-HSDL2 Antibody Picoband® IF analysis of HSDL2 using anti-HSDL2 antibody (A11317-1). HSDL2 was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HSDL2 Antibody (A11317-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11317-1-hsdl2-primary-antibodies-fcm-testing-12.pngAnti-HSDL2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-HSDL2 antibody (A11317-1). Overlay histogram showing HepG2 cells stained with A11317-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSDL2 Antibody (A11317-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hspa12a-picoband-trade-antibody-a13632-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13632-1-hspa12a-primary-antibodies-wb-testing-1.jpgAnti-HSPA12A Antibody Picoband® Western blot analysis of HSPA12A using anti-HSPA12A antibody (A13632-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA12A antigen affinity purified polyclonal antibody (Catalog # A13632-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSPA12A at approximately 75 kDa. The expected band size for HSPA12A is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13632-1-hspa12a-primary-antibodies-if-testing-2.jpgAnti-HSPA12A Antibody Picoband® IF analysis of HSPA12A using anti-HSPA12A antibody (A13632-1). HSPA12A was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HSPA12A Antibody (A13632-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-hspa4l-picoband-trade-antibody-a10753-1-boster.html2026-03-16T09:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10753-1-hspa4l-primary-antibodies-wb-testing-1.jpgAnti-HSPA4L Antibody Picoband® Western blot analysis of HSPA4L using anti-HSPA4L antibody (A10753-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA4L antigen affinity purified polyclonal antibody (Catalog # A10753-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSPA4L at approximately 95 kDa. The expected band size for HSPA4L is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10753-1-hspa4l-primary-antibodies-ihc-testing-1.jpgAnti-HSPA4L Antibody Picoband®IHC analysis of HSPA4L using anti-HSPA4L antibody (A10753-1). HSPA4L was detected in a paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSPA4L Antibody (A10753-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10753-1-hspa4l-primary-antibodies-if-testing-2.jpgAnti-HSPA4L Antibody Picoband® IF analysis of HSPA4L using anti-HSPA4L antibody (A10753-1). HSPA4L was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HSPA4L Antibody (A10753-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10753-1-hspa4l-primary-antibodies-fcm-testing-3.pngAnti-HSPA4L Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-HSPA4L antibody (A10753-1). Overlay histogram showing 293T cells stained with A10753-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSPA4L Antibody (A10753-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10753-1-hspa4l-primary-antibodies-fcm-testing-4.pngAnti-HSPA4L Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-HSPA4L antibody (A10753-1). Overlay histogram showing Hela cells stained with A10753-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSPA4L Antibody (A10753-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-islet-1-isl1-picoband-trade-antibody-a02969-3-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02969-3-isl1-primary-antibodies-wb-testing-1.jpgAnti-Islet 1/ISL1 Antibody Picoband® Western blot analysis of Islet 1/ISL1 using anti-Islet 1/ISL1 antibody (A02969-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Islet 1/ISL1 antigen affinity purified polyclonal antibody (Catalog # A02969-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Islet 1/ISL1 at approximately 42 kDa. The expected band size for Islet 1/ISL1 is at 39,45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02969-3-isl1-primary-antibodies-ihc-testing-2.jpgAnti-Islet 1/ISL1 Antibody Picoband® IHC analysis of Islet 1/ISL1 using anti-Islet 1/ISL1 antibody (A02969-3). Islet 1/ISL1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Islet 1/ISL1 Antibody (A02969-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02969-3-isl1-primary-antibodies-ihc-testing-3.jpgAnti-Islet 1/ISL1 Antibody Picoband® IHC analysis of Islet 1/ISL1 using anti-Islet 1/ISL1 antibody (A02969-3). Islet 1/ISL1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Islet 1/ISL1 Antibody (A02969-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02969-3-isl1-primary-antibodies-if-testing-4.jpgAnti-Islet 1/ISL1 Antibody Picoband® IF analysis of Islet 1/ISL1 using anti-Islet 1/ISL1 antibody (A02969-3) and anti-Beta Tubulin antibody (M01857-3). Islet 1/ISL1 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Islet 1/ISL1 Antibody (A02969-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02969-3-isl1-primary-antibodies-if-testing-5.jpgAnti-Islet 1/ISL1 Antibody Picoband® IF analysis of Islet 1/ISL1 using anti-Islet 1/ISL1 antibody (A02969-3). Islet 1/ISL1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Islet 1/ISL1 Antibody (A02969-3) overnight at 4°C. FITC Conjugated Goat Anti-Rabbit IgG (BA1105) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02969-3-isl1-primary-antibodies-if-testing-6.jpgAnti-Islet 1/ISL1 Antibody Picoband® IF analysis of Islet 1/ISL1 using anti-Islet 1/ISL1 antibody (A02969-3). Islet 1/ISL1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Islet 1/ISL1 Antibody (A02969-3) overnight at 4°C. FITC Conjugated Goat Anti-Rabbit IgG (BA1105) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-huntingtin-htt-picoband-trade-antibody-a00134-2-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00134-2-htt-primary-antibodies-ihc-testing-1.jpgAnti-Huntingtin/HTT Antibody IHC analysis of Huntingtin/HTT using anti-Huntingtin/HTT antibody (A00134-2). Huntingtin/HTT was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Huntingtin/HTT Antibody (A00134-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00134-2-htt-primary-antibodies-ihc-testing-2.jpgAnti-Huntingtin/HTT Antibody IHC analysis of Huntingtin/HTT using anti-Huntingtin/HTT antibody (A00134-2). Huntingtin/HTT was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Huntingtin/HTT Antibody (A00134-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00134-2-htt-primary-antibodies-ihc-testing-3.jpgAnti-Huntingtin/HTT Antibody IHC analysis of Huntingtin/HTT using anti-Huntingtin/HTT antibody (A00134-2). Huntingtin/HTT was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Huntingtin/HTT Antibody (A00134-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00134-2-htt-primary-antibodies-ihc-testing-4.jpgAnti-Huntingtin/HTT Antibody IHC analysis of Huntingtin/HTT using anti-Huntingtin/HTT antibody (A00134-2). Huntingtin/HTT was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Huntingtin/HTT Antibody (A00134-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00134-2-htt-primary-antibodies-ihc-testing-5.jpgAnti-Huntingtin/HTT Antibody IHC analysis of Huntingtin/HTT using anti-Huntingtin/HTT antibody (A00134-2). Huntingtin/HTT was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Huntingtin/HTT Antibody (A00134-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00134-2-htt-primary-antibodies-ihc-testing-6.jpgAnti-Huntingtin/HTT Antibody IHC analysis of Huntingtin/HTT using anti-Huntingtin/HTT antibody (A00134-2). Huntingtin/HTT was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Huntingtin/HTT Antibody (A00134-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00134-2-htt-primary-antibodies-ihc-testing-7.jpgAnti-Huntingtin/HTT Antibody IHC analysis of Huntingtin/HTT using anti-Huntingtin/HTT antibody (A00134-2). Huntingtin/HTT was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Huntingtin/HTT Antibody (A00134-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-smim8-picoband-trade-antibody-a17404-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-1.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-2.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human diffuse large B cell lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-3.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human laryngeal squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-4.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-5.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-6.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-7.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-8.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17404-smim8-primary-antibodies-ihc-testing-9.jpgAnti-SMIM8 Antibody IHC analysis of SMIM8 using anti-SMIM8 antibody (A17404). SMIM8 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SMIM8 Antibody (A17404) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-rasgrp3-picoband-trade-antibody-a07245-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07245-1-rasgrp3-primary-antibodies-ihc-testing-1.jpgAnti-RASGRP3 Antibody IHC analysis of RASGRP3 using anti-RASGRP3 antibody (A07245-1). RASGRP3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RASGRP3 Antibody (A07245-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07245-1-rasgrp3-primary-antibodies-ihc-testing-2.jpgAnti-RASGRP3 Antibody IHC analysis of RASGRP3 using anti-RASGRP3 antibody (A07245-1). RASGRP3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RASGRP3 Antibody (A07245-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07245-1-rasgrp3-primary-antibodies-ihc-testing-3.jpgAnti-RASGRP3 Antibody IHC analysis of RASGRP3 using anti-RASGRP3 antibody (A07245-1). RASGRP3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RASGRP3 Antibody (A07245-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07245-1-rasgrp3-primary-antibodies-ihc-testing-4.jpgAnti-RASGRP3 Antibody IHC analysis of RASGRP3 using anti-RASGRP3 antibody (A07245-1). RASGRP3 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RASGRP3 Antibody (A07245-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-ocm-picoband-trade-antibody-a06253-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06253-1-ocm-primary-antibodies-ihc-testing-1.jpgAnti-OCM Antibody IHC analysis of OCM using anti-OCM antibody (A06253-1). OCM was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OCM Antibody (A06253-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06253-1-ocm-primary-antibodies-ihc-testing-2.jpgAnti-OCM Antibody IHC analysis of OCM using anti-OCM antibody (A06253-1). OCM was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OCM Antibody (A06253-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06253-1-ocm-primary-antibodies-ihc-testing-3.jpgAnti-OCM Antibody IHC analysis of OCM using anti-OCM antibody (A06253-1). OCM was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OCM Antibody (A06253-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06253-1-ocm-primary-antibodies-ihc-testing-4.jpgAnti-OCM Antibody IHC analysis of OCM using anti-OCM antibody (A06253-1). OCM was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OCM Antibody (A06253-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06253-1-ocm-primary-antibodies-ihc-testing-5.jpgAnti-OCM Antibody IHC analysis of OCM using anti-OCM antibody (A06253-1). OCM was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OCM Antibody (A06253-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06253-1-ocm-primary-antibodies-ihc-testing-6.jpgAnti-OCM Antibody IHC analysis of OCM using anti-OCM antibody (A06253-1). OCM was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OCM Antibody (A06253-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06253-1-ocm-primary-antibodies-ihc-testing-7.jpgAnti-OCM Antibody IHC analysis of OCM using anti-OCM antibody (A06253-1). OCM was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OCM Antibody (A06253-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-golga7-picoband-trade-antibody-a10740-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10740-1-golga7-primary-antibodies-ihc-testing-1.jpgAnti-GOLGA7 Antibody IHC analysis of GOLGA7 using anti-GOLGA7 antibody (A10740-1). GOLGA7 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GOLGA7 Antibody (A10740-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10740-1-golga7-primary-antibodies-ihc-testing-2.jpgAnti-GOLGA7 Antibody IHC analysis of GOLGA7 using anti-GOLGA7 antibody (A10740-1). GOLGA7 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GOLGA7 Antibody (A10740-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10740-1-golga7-primary-antibodies-ihc-testing-3.jpgAnti-GOLGA7 Antibody IHC analysis of GOLGA7 using anti-GOLGA7 antibody (A10740-1). GOLGA7 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GOLGA7 Antibody (A10740-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10740-1-golga7-primary-antibodies-ihc-testing-4.jpgAnti-GOLGA7 Antibody IHC analysis of GOLGA7 using anti-GOLGA7 antibody (A10740-1). GOLGA7 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GOLGA7 Antibody (A10740-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10740-1-golga7-primary-antibodies-ihc-testing-5.jpgAnti-GOLGA7 Antibody IHC analysis of GOLGA7 using anti-GOLGA7 antibody (A10740-1). GOLGA7 was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GOLGA7 Antibody (A10740-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10740-1-golga7-primary-antibodies-ihc-testing-6.jpgAnti-GOLGA7 Antibody IHC analysis of GOLGA7 using anti-GOLGA7 antibody (A10740-1). GOLGA7 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GOLGA7 Antibody (A10740-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10740-1-golga7-primary-antibodies-ihc-testing-7.jpgAnti-GOLGA7 Antibody IHC analysis of GOLGA7 using anti-GOLGA7 antibody (A10740-1). GOLGA7 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GOLGA7 Antibody (A10740-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-s100a12-picoband-trade-antibody-a01478-1-boster.html2026-03-17T05:15:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01478-1-s100a12-primary-antibodies-ihc-testing-1.jpgAnti-S100A12 Antibody IHC analysis of S100A12 using anti-S100A12 antibody (A01478-1). S100A12 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-S100A12 Antibody (A01478-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01478-1-s100a12-primary-antibodies-ihc-testing-2.jpgAnti-S100A12 Antibody IHC analysis of S100A12 using anti-S100A12 antibody (A01478-1). S100A12 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-S100A12 Antibody (A01478-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01478-1-s100a12-primary-antibodies-ihc-testing-3.jpgAnti-S100A12 Antibody IHC analysis of S100A12 using anti-S100A12 antibody (A01478-1). S100A12 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-S100A12 Antibody (A01478-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-hcrt-picoband-trade-antibody-a01633-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-1.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-2.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-3.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-4.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-5.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-6.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-7.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-8.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-9.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-ihc-testing-10.jpgAnti-HCRT Antibody IHC analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-if-testing-11.jpgAnti-HCRT Antibody IF analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01633-1-hcrt-primary-antibodies-if-testing-12.jpgAnti-HCRT Antibody IF analysis of HCRT using anti-HCRT antibody (A01633-1). HCRT was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HCRT Antibody (A01633-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/all-secondary-antibodies/fluoro-594-conjugated-affinipure-rabbit-igg-ba1045-fluoro594-boster.html2026-03-10T04:36:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box_16_2.pngFluoro594 Conjugated AffiniPure Rabbit IgG (H+L)Boster Kit Box https://www.bosterbio.com/catalog/product/view/id/1253832026-03-10T04:36:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2263.jpgMouse MARCO ELISA Kit PicoKine®Mouse MARCO PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1253842026-03-10T04:36:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2264.pngHuman PCDH17 ELISA Kit PicoKine®Human PCDH17 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1253852026-03-10T04:36:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2265.jpgHuman PDGFRA ELISA Kit PicoKine®Human PDGFRA PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1253862026-03-10T04:36:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2266.jpgHuman PEAR1 ELISA Kit PicoKine®Human PEAR1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1253872026-03-10T04:36:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2267.jpgHuman PGLYRP1 ELISA Kit PicoKine®Human PGLYRP1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-h1-10-picoband-trade-antibody-a12456-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12456-1-h1fx-primary-antibodies-wb-testing-1.jpgAnti-H1-10 Antibody Picoband® Western blot analysis of H1-10 using anti-H1-10 antibody (A12456-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-H1-10 antigen affinity purified polyclonal antibody (Catalog # A12456-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for H1-10 at approximately 30 kDa. The expected band size for H1-10 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12456-1-h1fx-primary-antibodies-if-testing-2.jpgAnti-H1-10 Antibody Picoband® IF analysis of H1-10 using anti-H1-10 antibody (A12456-1) and anti-Beta Tubulin antibody (M01857-3). H1-10 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-H1-10 Antibody (A12456-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-h2afy-macroh2a1-picoband-trade-antibody-a04635-3-boster.html2026-03-25T05:24:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-wb-testing-1.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® Western blot analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat thymus tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-H2AFY/MACROH2A1 antigen affinity purified polyclonal antibody (Catalog # A04635-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for H2AFY/MACROH2A1 at approximately 39 kDa. The expected band size for H2AFY/MACROH2A1 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-2.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-3.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-4.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-5.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-6.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-7.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-8.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-ihc-testing-9.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IHC analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3). H2AFY/MACROH2A1 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04635-3-h2afy-primary-antibodies-if-testing-10.jpgAnti-H2AFY/MACROH2A1 Antibody Picoband® IF analysis of H2AFY/MACROH2A1 using anti-H2AFY/MACROH2A1 antibody (A04635-3) and anti-Beta Tubulin antibody (M01857-3). H2AFY/MACROH2A1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-H2AFY/MACROH2A1 Antibody (A04635-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-h2afy2-macroh2a2-picoband-trade-antibody-a09931-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09931-1-h2afy2-primary-antibodies-wb-testing-1.jpgAnti-H2AFY2/MACROH2A2 Antibody Picoband® Western blot analysis of H2AFY2/MACROH2A2 using anti-H2AFY2/MACROH2A2 antibody (A09931-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-H2AFY2/MACROH2A2 antigen affinity purified polyclonal antibody (Catalog # A09931-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for H2AFY2/MACROH2A2 at approximately 40 kDa. The expected band size for H2AFY2/MACROH2A2 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09931-1-h2afy2-primary-antibodies-ihc-testing-2.jpgAnti-H2AFY2/MACROH2A2 Antibody Picoband® IHC analysis of H2AFY2/MACROH2A2 using anti-H2AFY2/MACROH2A2 antibody (A09931-1). H2AFY2/MACROH2A2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY2/MACROH2A2 Antibody (A09931-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09931-1-h2afy2-primary-antibodies-ihc-testing-3.jpgAnti-H2AFY2/MACROH2A2 Antibody Picoband® IHC analysis of H2AFY2/MACROH2A2 using anti-H2AFY2/MACROH2A2 antibody (A09931-1). H2AFY2/MACROH2A2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY2/MACROH2A2 Antibody (A09931-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09931-1-h2afy2-primary-antibodies-ihc-testing-4.jpgAnti-H2AFY2/MACROH2A2 Antibody Picoband® IHC analysis of H2AFY2/MACROH2A2 using anti-H2AFY2/MACROH2A2 antibody (A09931-1). H2AFY2/MACROH2A2 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-H2AFY2/MACROH2A2 Antibody (A09931-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09931-1-h2afy2-primary-antibodies-if-testing-5.jpgAnti-H2AFY2/MACROH2A2 Antibody Picoband® IF analysis of H2AFY2/MACROH2A2 using anti-H2AFY2/MACROH2A2 antibody (A09931-1) and anti-Beta Tubulin antibody (M01857-3). H2AFY2/MACROH2A2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-H2AFY2/MACROH2A2 Antibody (A09931-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09931-1-h2afy2-primary-antibodies-fcm-testing-6.pngAnti-H2AFY2/MACROH2A2 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-H2AFY2/MACROH2A2 antibody (A09931-1). Overlay histogram showing PC-3 cells stained with A09931-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-H2AFY2/MACROH2A2 Antibody (A09931-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-haao-picoband-trade-antibody-a10482-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10482-1-haao-primary-antibodies-wb-testing-1.jpgAnti-HAAO Antibody Picoband® Western blot analysis of HAAO using anti-HAAO antibody (A10482-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human hepatocellular carcinoma paracancerous (HCCP) tissue lysates, Lane 2: rat liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HAAO antigen affinity purified polyclonal antibody (Catalog # A10482-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HAAO at approximately 33 kDa. The expected band size for HAAO is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10482-1-haao-primary-antibodies-if-testing-2.jpgAnti-HAAO Antibody Picoband® IF analysis of HAAO using anti-HAAO antibody (A10482-1). HAAO was detected in an immunocytochemical section of Caco-2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HAAO Antibody (A10482-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-hadh-picoband-trade-antibody-a03650-1-boster.html2026-03-16T09:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-wb-testing-1.jpgAnti-HADH Antibody Picoband® Western blot analysis of HADH using anti-HADH antibody (A03650-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HADH antigen affinity purified polyclonal antibody (Catalog # A03650-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HADH at approximately 34 kDa. The expected band size for HADH is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-2.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-3.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-4.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-5.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-6.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-7.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-8.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-9.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-10.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-11.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-12.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-13.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-14.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-15.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-16.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-17.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-18.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of rat alcohol liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-ihc-testing-19.jpgAnti-HADH Antibody Picoband® IHC analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of rat alcohol liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-if-testing-20.jpgAnti-HADH Antibody Picoband® IF analysis of HADH using anti-HADH antibody (A03650-1). HADH was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-if-testing-21.jpgAnti-HADH Antibody Picoband® IF analysis of HADH using antiHADH antibody (A03650-1). HADH was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HADH Antibody (A03650-1) overnight at 4°C. Biotin conjugated goat anti-rabbit IgG (BA1003) was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using DyLight®550 Conjugated Avidin (BA1134). The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03650-1-hadh-primary-antibodies-fcm-testing-22.pngAnti-HADH Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-HADH antibody (A03650-1). Overlay histogram showing HepG2 cells stained with A03650-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HADH Antibody (A03650-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hadhb-picoband-trade-antibody-a04776-2-boster.html2026-03-16T09:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-wb-testing-1.jpgAnti-HADHB Antibody Picoband® Western blot analysis of HADHB using anti-HADHB antibody (A04776-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat skeletal muscle tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HADHB antigen affinity purified polyclonal antibody (Catalog # A04776-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HADHB at approximately 45 kDa. The expected band size for HADHB is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-2.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-3.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-4.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-5.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-6.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-7.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-8.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-9.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-10.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-ihc-testing-11.jpgAnti-HADHB Antibody Picoband® IHC analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-if-testing-12.jpgAnti-HADHB Antibody Picoband® IF analysis of HADHB using anti-HADHB antibody (A04776-2). HADHB was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HADHB Antibody (A04776-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04776-2-hadhb-primary-antibodies-fcm-testing-13.pngAnti-HADHB Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-HADHB antibody (A04776-2). Overlay histogram showing HepG2 cells stained with A04776-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HADHB Antibody (A04776-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hagh-picoband-trade-antibody-a08943-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-wb-testing-1.jpgAnti-HAGH Antibody Picoband® Western blot analysis of HAGH using anti-HAGH antibody (A08943-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HAGH antigen affinity purified polyclonal antibody (Catalog # A08943-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HAGH at approximately 29 kDa. The expected band size for HAGH is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-2.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-3.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-4.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-5.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-6.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-7.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-8.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-9.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-ihc-testing-10.jpgAnti-HAGH Antibody Picoband® IHC analysis of HAGH using anti-HAGH antibody (A08943-1). HAGH was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAGH Antibody (A08943-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-fcm-testing-11.pngAnti-HAGH Antibody Picoband® Flow Cytometry analysis of JK cells using anti-HAGH antibody (A08943-1). Overlay histogram showing JK cells stained with A08943-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HAGH Antibody (A08943-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08943-1-hagh-primary-antibodies-fcm-testing-12.pngAnti-HAGH Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-HAGH antibody (A08943-1). Overlay histogram showing U20S cells stained with A08943-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HAGH Antibody (A08943-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hao1-picoband-trade-antibody-a09159-2-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09159-2-hao1-primary-antibodies-wb-testing-1.jpgAnti-HAO1 Antibody Picoband® Western blot analysis of HAO1 using anti-HAO1 antibody (A09159-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HAO1 antigen affinity purified polyclonal antibody (Catalog # A09159-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HAO1 at approximately 41 kDa. The expected band size for HAO1 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09159-2-hao1-primary-antibodies-ihc-testing-4.jpgAnti-HAO1 Antibody Picoband®IHC analysis of HAO1 using anti-HAO1 antibody (A09159-2). HAO1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAO1 Antibody (A09159-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09159-2-hao1-primary-antibodies-ihc-testing-2.jpgAnti-HAO1 Antibody Picoband® IHC analysis of HAO1 using anti-HAO1 antibody (A09159-2). HAO1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAO1 Antibody (A09159-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09159-2-hao1-primary-antibodies-ihc-testing-3.jpgAnti-HAO1 Antibody Picoband® IHC analysis of HAO1 using anti-HAO1 antibody (A09159-2). HAO1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HAO1 Antibody (A09159-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09159-2-hao1-primary-antibodies-fcm-testing-4.pngAnti-HAO1 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-HAO1 antibody (A09159-2). Overlay histogram showing SiHa cells stained with A09159-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HAO1 Antibody (A09159-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hao2-picoband-trade-antibody-a11930-2-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11930-2-hao2-primary-antibodies-wb-testing-1.jpgAnti-HAO2 Antibody Picoband® Western blot analysis of HAO2 using anti-HAO2 antibody (A11930-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HAO2 antigen affinity purified polyclonal antibody (Catalog # A11930-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HAO2 at approximately 39 kDa. The expected band size for HAO2 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11930-2-hao2-primary-antibodies-fcm-testing-2.pngAnti-HAO2 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-HAO2 antibody (A11930-2). Overlay histogram showing 293T cells stained with A11930-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HAO2 Antibody (A11930-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-haus3-picoband-trade-antibody-a12796-2-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12796-2-haus3-primary-antibodies-wb-testing-1.jpgAnti-HAUS3 Antibody Picoband® Western blot analysis of HAUS3 using anti-HAUS3 antibody (A12796-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HAUS3 antigen affinity purified polyclonal antibody (Catalog # A12796-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HAUS3 at approximately 55 kDa. The expected band size for HAUS3 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12796-2-haus3-primary-antibodies-if-testing-2.jpgAnti-HAUS3 Antibody Picoband® IF analysis of HAUS3 using anti-HAUS3 antibody (A12796-2). HAUS3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HAUS3 Antibody (A12796-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12796-2-haus3-primary-antibodies-fcm-testing-3.pngAnti-HAUS3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-HAUS3 antibody (A12796-2). Overlay histogram showing HepG2 cells stained with A12796-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HAUS3 Antibody (A12796-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-uchl5ip-haus7-picoband-trade-antibody-a12338-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12338-1-haus7-primary-antibodies-wb-testing-1.jpgAnti-UCHL5IP/HAUS7 Antibody Picoband® Western blot analysis of UCHL5IP/HAUS7 using anti-UCHL5IP/HAUS7 antibody (A12338-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UCHL5IP/HAUS7 antigen affinity purified polyclonal antibody (Catalog # A12338-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for UCHL5IP/HAUS7 at approximately 46 kDa. The expected band size for UCHL5IP/HAUS7 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12338-1-haus7-primary-antibodies-if-testing-2.jpgAnti-UCHL5IP/HAUS7 Antibody Picoband® IF analysis of UCHL5IP/HAUS7 using anti-UCHL5IP/HAUS7 antibody (A12338-1). UCHL5IP/HAUS7 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-UCHL5IP/HAUS7 Antibody (A12338-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12338-1-haus7-primary-antibodies-fcm-testing-3.pngAnti-UCHL5IP/HAUS7 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-UCHL5IP/HAUS7 antibody (A12338-1). Overlay histogram showing MCF-7 cells stained with A12338-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-UCHL5IP/HAUS7 Antibody (A12338-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hbq1-picoband-trade-antibody-a14380-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14380-1-hbq1-primary-antibodies-wb-testing-1.jpgAnti-HBQ1 Antibody Picoband® Western blot analysis of HBQ1 using anti-HBQ1 antibody (A14380-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HBQ1 antigen affinity purified polyclonal antibody (Catalog # A14380-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HBQ1 at approximately 16 kDa. The expected band size for HBQ1 is at 16 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-hddc2-picoband-trade-antibody-a08033-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08033-1-hddc2-primary-antibodies-wb-testing-1.jpgAnti-HDDC2 Antibody Picoband® Western blot analysis of HDDC2 using anti-HDDC2 antibody (A08033-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDDC2 antigen affinity purified polyclonal antibody (Catalog # A08033-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDDC2 at approximately 26 kDa. The expected band size for HDDC2 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08033-1-hddc2-primary-antibodies-if-testing-2.jpgAnti-HDDC2 Antibody Picoband® IF analysis of HDDC2 using anti-HDDC2 antibody (A08033-1). HDDC2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HDDC2 Antibody (A08033-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08033-1-hddc2-primary-antibodies-fcm-testing-3.pngAnti-HDDC2 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-HDDC2 antibody (A08033-1). Overlay histogram showing SiHa cells stained with A08033-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HDDC2 Antibody (A08033-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hdgfl2-picoband-trade-antibody-a32401-2-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32401-2-hdgfl2-primary-antibodies-wb-testing-1.jpgAnti-HDGFL2 Antibody Picoband® Western blot analysis of HDGFL2 using anti-HDGFL2 antibody (A32401-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDGFL2 antigen affinity purified polyclonal antibody (Catalog # A32401-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDGFL2 at approximately 140 kDa. The expected band size for HDGFL2 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32401-2-hdgfl2-primary-antibodies-if-testing-2.jpgAnti-HDGFL2 Antibody Picoband® IF analysis of HDGFL2 using anti-HDGFL2 antibody (A32401-2). HDGFL2 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HDGFL2 Antibody (A32401-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32401-2-hdgfl2-primary-antibodies-fcm-testing-3.pngAnti-HDGFL2 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-HDGFL2 antibody (A32401-2). Overlay histogram showing PC-3 cells stained with A32401-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HDGFL2 Antibody (A32401-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hdhd2-picoband-trade-antibody-a15632-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-wb-testing-1.jpgAnti-HDHD2 Antibody Picoband® Western blot analysis of HDHD2 using anti-HDHD2 antibody (A15632-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDHD2 antigen affinity purified polyclonal antibody (Catalog # A15632-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDHD2 at approximately 28 kDa. The expected band size for HDHD2 is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-ihc-testing-2.jpgAnti-HDHD2 Antibody Picoband® IHC analysis of HDHD2 using anti-HDHD2 antibody (A15632-1). HDHD2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD2 Antibody (A15632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-ihc-testing-3.jpgAnti-HDHD2 Antibody Picoband® IHC analysis of HDHD2 using anti-HDHD2 antibody (A15632-1). HDHD2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD2 Antibody (A15632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-ihc-testing-4.jpgAnti-HDHD2 Antibody Picoband® IHC analysis of HDHD2 using anti-HDHD2 antibody (A15632-1). HDHD2 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD2 Antibody (A15632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-ihc-testing-5.jpgAnti-HDHD2 Antibody Picoband® IHC analysis of HDHD2 using anti-HDHD2 antibody (A15632-1). HDHD2 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD2 Antibody (A15632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-ihc-testing-6.jpgAnti-HDHD2 Antibody Picoband® IHC analysis of HDHD2 using anti-HDHD2 antibody (A15632-1). HDHD2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD2 Antibody (A15632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-ihc-testing-7.jpgAnti-HDHD2 Antibody Picoband® IHC analysis of HDHD2 using anti-HDHD2 antibody (A15632-1). HDHD2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD2 Antibody (A15632-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15632-1-hdhd2-primary-antibodies-fcm-testing-8.pngAnti-HDHD2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-HDHD2 antibody (A15632-1). Overlay histogram showing JK cells stained with A15632-1(Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-HDHD2 Antibody (A15632-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hdhd5-picoband-trade-antibody-a31869-1-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-wb-testing-1.jpgAnti-HDHD5 Antibody Picoband® Western blot analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDHD5 antigen affinity purified polyclonal antibody (Catalog # A31869-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDHD5 at approximately 50 kDa. The expected band size for HDHD5 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-2.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-3.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-4.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of human ovarian tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-5.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of human ovarian tumor tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-6.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-7.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-8.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of mouse brain(cerebral cortex) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-9.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of mouse brain(hippocampus) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-10.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of rat brain(cerebral cortex) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-ihc-testing-11.jpgAnti-HDHD5 Antibody Picoband® IHC analysis of HDHD5 using anti-HDHD5 antibody (A31869-1). HDHD5 was detected in a paraffin-embedded section of rat brain(hippocampus) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HDHD5 Antibody (A31869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31869-1-hdhd5-primary-antibodies-fcm-testing-12.pngAnti-HDHD5 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-HDHD5 antibody (A31869-1). Overlay histogram showing JK cells stained with A31869-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HDHD5 Antibody (A31869-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hdlbp-picoband-trade-antibody-a06727-2-boster.html2026-03-17T05:15:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06727-2-hdlbp-primary-antibodies-wb-testing-1.jpgAnti-HDLBP Antibody Picoband® Western blot analysis of HDLBP using anti-HDLBP antibody (A06727-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDLBP antigen affinity purified polyclonal antibody (Catalog # A06727-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDLBP at approximately 150 kDa. The expected band size for HDLBP is at 141 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06727-2-hdlbp-primary-antibodies-if-testing-2.jpgAnti-HDLBP Antibody Picoband® IF analysis of HDLBP using anti-HDLBP antibody (A06727-2). HDLBP was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HDLBP Antibody (A06727-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06727-2-hdlbp-primary-antibodies-fcm-testing-3.pngAnti-HDLBP Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-HDLBP antibody (A06727-2). Overlay histogram showing 293T cells stained with A06727-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HDLBP Antibody (A06727-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hebp1-picoband-trade-antibody-a00271-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00271-1-hebp1-primary-antibodies-wb-testing-1.jpgAnti-HEBP1 Antibody Picoband® Western blot analysis of HEBP1 using anti-HEBP1 antibody (A00271-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human hepatocellular carcinoma tumor tissue (HCCT) lysates, Lane 4: human hepatocellular carcinoma paracancerous tissue (HCCP) lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HEBP1 antigen affinity purified polyclonal antibody (Catalog # A00271-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HEBP1 at approximately 21 kDa. The expected band size for HEBP1 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00271-1-hebp1-primary-antibodies-ihc-testing-2.jpgAnti-HEBP1 Antibody Picoband® IHC analysis of HEBP1 using anti-HEBP1 antibody (A00271-1). HEBP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HEBP1 Antibody (A00271-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00271-1-hebp1-primary-antibodies-ihc-testing-3.jpgAnti-HEBP1 Antibody Picoband® IHC analysis of HEBP1 using anti-HEBP1 antibody (A00271-1). HEBP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HEBP1 Antibody (A00271-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00271-1-hebp1-primary-antibodies-if-testing-4.jpgAnti-HEBP1 Antibody Picoband® IF analysis of HEBP1 using anti-HEBP1 antibody (A00271-1). HEBP1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HEBP1 Antibody (A00271-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00271-1-hebp1-primary-antibodies-fcm-testing-5.pngAnti-HEBP1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-HEBP1 antibody (A00271-1). Overlay histogram showing A549 cells stained with A00271-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HEBP1 Antibody (A00271-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hells-picoband-trade-antibody-a04702-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04702-1-hells-primary-antibodies-wb-testing-1.jpgAnti-HELLS Antibody Picoband® Western blot analysis of HELLS using anti-HELLS antibody (A04702-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: mouse thymus tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HELLS antigen affinity purified polyclonal antibody (Catalog # A04702-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HELLS at approximately 97 kDa. The expected band size for HELLS is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04702-1-hells-primary-antibodies-if-testing-2.jpgAnti-HELLS Antibody Picoband® IF analysis of HELLS using anti-HELLS antibody (A04702-1) and anti-Beta Tubulin antibody (M01857-3). HELLS was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HELLS Antibody (A04702-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04702-1-hells-primary-antibodies-fcm-testing-3.pngAnti-HELLS Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-HELLS antibody (A04702-1). Overlay histogram showing PC-3 cells stained with A04702-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HELLS Antibody (A04702-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-helz-picoband-trade-antibody-a09181-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09181-1-helz-primary-antibodies-wb-testing-1.jpgAnti-HELZ Antibody Picoband® Western blot analysis of HELZ using anti-HELZ antibody (A09181-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HELZ antigen affinity purified polyclonal antibody (Catalog # A09181-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HELZ at approximately 200 kDa. The expected band size for HELZ is at 219 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09181-1-helz-primary-antibodies-if-testing-2.jpgAnti-HELZ Antibody Picoband® IF analysis of HELZ using anti-HELZ antibody (A09181-1). HELZ was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HELZ Antibody (A09181-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09181-1-helz-primary-antibodies-fcm-testing-3.pngAnti-HELZ Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-HELZ antibody (A09181-1). Overlay histogram showing Hela cells stained with A09181-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HELZ Antibody (A09181-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09181-1-helz-primary-antibodies-fcm-testing-4.pngAnti-HELZ Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-HELZ antibody (A09181-1). Overlay histogram showing MCF-7 cells stained with A09181-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HELZ Antibody (A09181-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-henmt1-picoband-trade-antibody-a14219-2-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14219-2-henmt1-primary-antibodies-wb-testing-1.jpgAnti-HENMT1 Antibody Picoband® Western blot analysis of HENMT1 using anti-HENMT1 antibody (A14219-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: mouse testis tissue lysates, Lane 5: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HENMT1 antigen affinity purified polyclonal antibody (Catalog # A14219-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HENMT1 at approximately 45 kDa. The expected band size for HENMT1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14219-2-henmt1-primary-antibodies-if-testing-2.jpgAnti-HENMT1 Antibody Picoband® IF analysis of HENMT1 using anti-HENMT1 antibody (A14219-2). HENMT1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HENMT1 Antibody (A14219-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14219-2-henmt1-primary-antibodies-fcm-testing-3.pngAnti-HENMT1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-HENMT1 antibody (A14219-2). Overlay histogram showing JK cells stained with A14219-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HENMT1 Antibody (A14219-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hspa1l-picoband-trade-antibody-a04286-3-boster.html2026-03-16T09:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-3-hspa1l-primary-antibodies-wb-testing-1.jpgAnti-HSPA1L Antibody Picoband® Western blot analysis of HSPA1L using anti-HSPA1L antibody (A04286-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA1L antigen affinity purified polyclonal antibody (Catalog # A04286-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSPA1L at approximately 70 kDa. The expected band size for HSPA1L is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-3-hspa1l-primary-antibodies-ihc-testing-2.jpgAnti-HSPA1L Antibody Picoband® IHC analysis of HSPA1L using anti-HSPA1L antibody (A04286-3). HSPA1L was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSPA1L Antibody (A04286-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-3-hspa1l-primary-antibodies-ihc-testing-3.jpgAnti-HSPA1L Antibody Picoband® IHC analysis of HSPA1L using anti-HSPA1L antibody (A04286-3). HSPA1L was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSPA1L Antibody (A04286-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-3-hspa1l-primary-antibodies-ihc-testing-4.jpgAnti-HSPA1L Antibody Picoband® IHC analysis of HSPA1L using anti-HSPA1L antibody (A04286-3). HSPA1L was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSPA1L Antibody (A04286-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-3-hspa1l-primary-antibodies-ihc-testing-5.jpgAnti-HSPA1L Antibody Picoband® IHC analysis of HSPA1L using anti-HSPA1L antibody (A04286-3). HSPA1L was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSPA1L Antibody (A04286-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-3-hspa1l-primary-antibodies-if-testing-6.jpgAnti-HSPA1L Antibody Picoband® IF analysis of HSPA1L using anti-HSPA1L antibody (A04286-3). HSPA1L was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HSPA1L Antibody (A04286-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04286-3-hspa1l-primary-antibodies-fcm-testing-7.pngAnti-HSPA1L Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-HSPA1L antibody (A04286-3). Overlay histogram showing HepG2 cells stained with A04286-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSPA1L Antibody (A04286-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ift172-picoband-trade-antibody-a08217-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08217-1-ift172-primary-antibodies-wb-testing-1.jpgAnti-IFT172 Antibody Picoband® Western blot analysis of IFT172 using anti-IFT172 antibody (A08217-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFT172 antigen affinity purified polyclonal antibody (Catalog # A08217-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFT172 at approximately 180 kDa. The expected band size for IFT172 is at 198 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-cd127-il7r-picoband-trade-antibody-a02222-3-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02222-3-il7r-primary-antibodies-wb-testing-1_1.jpgAnti-CD127/IL7R Antibody Picoband® Western blot analysis of CD127/IL7R using anti-CD127/IL7R antibody (A02222-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MOLT-4 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD127/IL7R antigen affinity purified polyclonal antibody (Catalog # A02222-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD127/IL7R at approximately 170 kDa. The expected band size for CD127/IL7R is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02222-3-il7r-primary-antibodies-ihc-testing-2.jpgAnti-CD127/IL7R Antibody Picoband® IHC analysis of CD127/IL7R using anti-CD127/IL7R antibody (A02222-3). CD127/IL7R was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD127/IL7R Antibody (A02222-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02222-3-il7r-primary-antibodies-ihc-testing-3.jpgAnti-CD127/IL7R Antibody Picoband® IHC analysis of CD127/IL7R using anti-CD127/IL7R antibody (A02222-3). CD127/IL7R was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD127/IL7R Antibody (A02222-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02222-3-il7r-primary-antibodies-ihc-testing-4.jpgAnti-CD127/IL7R Antibody Picoband® IHC analysis of CD127/IL7R using anti-CD127/IL7R antibody (A02222-3). CD127/IL7R was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD127/IL7R Antibody (A02222-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02222-3-il7r-primary-antibodies-ihc-testing-5.jpgAnti-CD127/IL7R Antibody Picoband® IHC analysis of CD127/IL7R using anti-CD127/IL7R antibody (A02222-3). CD127/IL7R was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD127/IL7R Antibody (A02222-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02222-3-il7r-primary-antibodies-fcm-testing-6_1.pngAnti-CD127/IL7R Antibody Picoband® Flow Cytometry analysis of JK cells using anti-CD127/IL7R antibody (A02222-3). Overlay histogram showing JK cells stained with A02222-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD127/IL7R Antibody (A02222-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-irs4-picoband-trade-antibody-a04616-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-wb-testing-1.jpgAnti-IRS4 Antibody Picoband® Western blot analysis of IRS4 using anti-IRS4 antibody (A04616-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: rat brain whole cell lysates, Lane 3: rat testis whole cell lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRS4 antigen affinity purified polyclonal antibody (Catalog # A04616-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRS4 at approximately 150 kDa. The expected band size for IRS4 is at 134 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-2.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-3.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-4.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-5.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-6.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-7.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-8.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-9_1.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-10.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-11.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-12.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-13.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-14.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-15.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-16.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-ihc-testing-17.jpgAnti-IRS4 Antibody Picoband® IHC analysis of IRS4 using anti-IRS4 antibody (A04616-1). IRS4 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRS4 Antibody (A04616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04616-1-irs4-primary-antibodies-fcm-testing-18.pngAnti-IRS4 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-IRS4 antibody (A04616-1). Overlay histogram showing Hela cells stained with A04616-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-IRS4 Antibody (A04616-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-hist1-ist1-picoband-trade-antibody-a05507-2-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-wb-testing-1.jpgAnti-hIST1/IST1 Antibody Picoband® Western blot analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human MRC-5 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse lung tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HIST1/IST1 antigen affinity purified polyclonal antibody (Catalog # A05507-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HIST1/IST1 at approximately 40 kDa. The expected band size for HIST1/IST1 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-2.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-3.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-4.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-5.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-6.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-7.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-8.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-ihc-testing-9.jpgAnti-hIST1/IST1 Antibody Picoband® IHC analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-if-testing-10.jpgAnti-hIST1/IST1 Antibody Picoband® IF analysis of HIST1/IST1 using anti-HIST1/IST1 antibody (A05507-2). HIST1/IST1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HIST1/IST1 Antibody (A05507-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05507-2-ist1-primary-antibodies-fcm-testing-11.pngAnti-hIST1/IST1 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-HIST1/IST1 antibody (A05507-2). Overlay histogram showing PC-3 cells stained with A05507-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HIST1/IST1 Antibody (A05507-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-itprip-picoband-trade-antibody-a11503-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11503-1-itprip-primary-antibodies-wb-testing-1.jpgAnti-ITPRIP Antibody Picoband® Western blot analysis of ITPRIP using anti-ITPRIP antibody (A11503-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissues lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITPRIP antigen affinity purified polyclonal antibody (Catalog # A11503-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITPRIP at approximately 80 kDa. The expected band size for ITPRIP is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11503-1-itprip-primary-antibodies-ihc-testing-2.jpgAnti-ITPRIP Antibody Picoband® IHC analysis of ITPRIP using anti-ITPRIP antibody (A11503-1). ITPRIP was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPRIP Antibody (A11503-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11503-1-itprip-primary-antibodies-ihc-testing-3.jpgAnti-ITPRIP Antibody Picoband® IHC analysis of ITPRIP using anti-ITPRIP antibody (A11503-1). ITPRIP was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ITPRIP Antibody (A11503-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11503-1-itprip-primary-antibodies-if-testing-4.jpgAnti-ITPRIP Antibody Picoband® IF analysis of ITPRIP using anti-ITPRIP antibody (A11503-1). ITPRIP was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ITPRIP Antibody (A11503-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-itpripl1-picoband-trade-antibody-a17509-2-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17509-2-itpripl1-primary-antibodies-wb-testing-1.jpgAnti-ITPRIPL1 Antibody Picoband® Western blot analysis of ITPRIPL1 using anti-ITPRIPL1 antibody (A17509-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITPRIPL1 antigen affinity purified polyclonal antibody (Catalog # A17509-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITPRIPL1 at approximately 70 kDa. The expected band size for ITPRIPL1 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17509-2-itpripl1-primary-antibodies-if-testing-2.jpgAnti-ITPRIPL1 Antibody Picoband® IF analysis of ITPRIPL1 using anti-ITPRIPL1 antibody (A17509-2). ITPRIPL1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ITPRIPL1 Antibody (A17509-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17509-2-itpripl1-primary-antibodies-fcm-testing-3.pngAnti-ITPRIPL1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-ITPRIPL1 antibody (A17509-2). Overlay histogram showing HEL cells stained with A17509-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ITPRIPL1 Antibody (A17509-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-intersectin-1-itsn1-picoband-trade-antibody-a03616-1-boster.html2026-03-16T09:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03616-1-itsn1-primary-antibodies-wb-testing-1.jpgAnti-Intersectin 1/ITSN1 Antibody Picoband® Western blot analysis of Intersectin 1/ITSN1 using anti-Intersectin 1/ITSN1 antibody (A03616-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Intersectin 1/ITSN1 antigen affinity purified polyclonal antibody (Catalog # A03616-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Intersectin 1/ITSN1 at approximately 150 kDa. The expected band size for Intersectin 1/ITSN1 is at 195 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03616-1-itsn1-primary-antibodies-ihc-testing-1.jpgAnti-Intersectin 1/ITSN1 Antibody Picoband®IHC analysis of Intersectin 1/ITSN1 using anti-Intersectin 1/ITSN1 antibody (A03616-1). Intersectin 1/ITSN1 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Intersectin 1/ITSN1 Antibody (A03616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03616-1-itsn1-primary-antibodies-if-testing-2.jpgAnti-Intersectin 1/ITSN1 Antibody Picoband® IF analysis of Intersectin 1/ITSN1 using anti-Intersectin 1/ITSN1 antibody (A03616-1). Intersectin 1/ITSN1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Intersectin 1/ITSN1 Antibody (A03616-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03616-1-itsn1-primary-antibodies-fcm-testing-3.pngAnti-Intersectin 1/ITSN1 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Intersectin 1/ITSN1 antibody (A03616-1). Overlay histogram showing SiHa cells stained with A03616-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Intersectin 1/ITSN1 Antibody (A03616-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-jagged-2-jag2-picoband-trade-antibody-a01428-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01428-1-jag2-primary-antibodies-wb-testing-1.jpgAnti-Jagged 2/JAG2 Antibody Picoband® Western blot analysis of Jagged 2/JAG2 using anti-Jagged 2/JAG2 antibody (A01428-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Jagged 2/JAG2 antigen affinity purified polyclonal antibody (Catalog # A01428-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Jagged 2/JAG2 at approximately 130 kDa. The expected band size for Jagged 2/JAG2 is at 133 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-lmo7dn-picoband-trade-antibody-a19130-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19130-lmo7dn-primary-antibodies-wb-testing-1.jpgAnti-LMO7DN Antibody Picoband® Western blot analysis of LMO7DN using anti-LMO7DN antibody (A19130). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMO7DN antigen affinity purified polyclonal antibody (Catalog # A19130) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LMO7DN at approximately 15 kDa. The expected band size for LMO7DN is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19130-lmo7dn-primary-antibodies-fcm-testing-2.pngAnti-LMO7DN Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-LMO7DN antibody (A19130). Overlay histogram showing Hela cells stained with A19130 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LMO7DN Antibody (A19130, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lrrc34-picoband-trade-antibody-a16000-1-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16000-1-lrrc34-primary-antibodies-wb-testing-1.jpgAnti-LRRC34 Antibody Picoband® Western blot analysis of LRRC34 using anti-LRRC34 antibody (A16000-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse testis tissue lysates, Lane 5: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC34 antigen affinity purified polyclonal antibody (Catalog # A16000-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC34 at approximately 43 kDa. The expected band size for LRRC34 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16000-1-lrrc34-primary-antibodies-ihc-testing-2.jpgAnti-LRRC34 Antibody Picoband® IF analysis of LRRC34 using anti-LRRC34 antibody (A16000-1). LRRC34 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LRRC34 Antibody (A16000-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16000-1-lrrc34-primary-antibodies-fcm-testing-3.pngAnti-LRRC34 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-LRRC34 antibody (A16000-1). Overlay histogram showing 293T cells stained with A16000-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LRRC34 Antibody (A16000-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mettl18-picoband-trade-antibody-a15133-boster.html2026-03-17T05:15:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-wb-testing-1.jpgAnti-METTL18 Antibody Picoband® Western blot analysis of METTL18 using anti-METTL18 antibody (A15133). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METTL18 antigen affinity purified polyclonal antibody (Catalog # A15133) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METTL18 at approximately 50 kDa. The expected band size for METTL18 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-ihc-testing-2.jpgAnti-METTL18 Antibody Picoband® IHC analysis of METTL18 using anti-METTL18 antibody (A15133). METTL18 was detected in a paraffin-embedded section of Diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METTL18 Antibody (A15133) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-ihc-testing-3.jpgAnti-METTL18 Antibody Picoband® IHC analysis of METTL18 using anti-METTL18 antibody (A15133). METTL18 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METTL18 Antibody (A15133) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-ihc-testing-4.jpgAnti-METTL18 Antibody Picoband® IHC analysis of METTL18 using anti-METTL18 antibody (A15133). METTL18 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METTL18 Antibody (A15133) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-ihc-testing-5.jpgAnti-METTL18 Antibody Picoband® IHC analysis of METTL18 using anti-METTL18 antibody (A15133). METTL18 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METTL18 Antibody (A15133) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-ihc-testing-6.jpgAnti-METTL18 Antibody Picoband® IHC analysis of METTL18 using anti-METTL18 antibody (A15133). METTL18 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-METTL18 Antibody (A15133) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-if-testing-7.jpgAnti-METTL18 Antibody Picoband® IF analysis of METTL18 using anti-METTL18 antibody (A15133) and anti-Beta Tubulin antibody (M01857-3). METTL18 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-METTL18 Antibody (A15133) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15133-mettl18-primary-antibodies-fcm-testing-8.pngAnti-METTL18 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-METTL18 antibody (A15133). Overlay histogram showing A431 cells stained with A15133 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-METTL18 Antibody (A15133, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mfsd3-picoband-trade-antibody-a19348-2-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19348-2-mfsd3-primary-antibodies-wb-testing-1.jpgAnti-MFSD3 Antibody Picoband® Western blot analysis of MFSD3 using anti-MFSD3 antibody (A19348-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MFSD3 antigen affinity purified polyclonal antibody (Catalog # A19348-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MFSD3 at approximately 43 kDa. The expected band size for MFSD3 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19348-2-mfsd3-primary-antibodies-fcm-testing-2.pngAnti-MFSD3 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MFSD3 antibody (A19348-2). Overlay histogram showing 293T cells stained with A19348-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MFSD3 Antibody (A19348-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mindy4-picoband-trade-antibody-a32449-1-boster.html2026-03-24T05:36:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32449-1-myndy4-primary-antibodies-wb-testing-1.jpgAnti-MINDY4 Antibody Picoband® Western blot analysis of MINDY4 using anti-MINDY4 antibody (A32449-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MINDY4 antigen affinity purified polyclonal antibody (Catalog # A32449-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MINDY4 at approximately 72 kDa. The expected band size for MINDY4 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32449-1-myndy4-primary-antibodies-ihc-testing-2.jpgAnti-MINDY4 Antibody Picoband® IHC analysis of MINDY4 using anti-MINDY4 antibody (A32449-1). MINDY4 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MINDY4 Antibody (A32449-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32449-1-myndy4-primary-antibodies-ihc-testing-3.jpgAnti-MINDY4 Antibody Picoband® IHC analysis of MINDY4 using anti-MINDY4 antibody (A32449-1). MINDY4 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MINDY4 Antibody (A32449-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-mipep-picoband-trade-antibody-a05926-1-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-wb-testing-1.jpgAnti-MIPEP Antibody Picoband® Western blot analysis of MIPEP using anti-MIPEP antibody (A05926-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIPEP antigen affinity purified polyclonal antibody (Catalog # A05926-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIPEP at approximately 80 kDa. The expected band size for MIPEP is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-ihc-testing-2.jpgAnti-MIPEP Antibody Picoband® IHC analysis of MIPEP using anti-MIPEP antibody (A05926-1). MIPEP was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIPEP Antibody (A05926-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-ihc-testing-3.jpgAnti-MIPEP Antibody Picoband® IHC analysis of MIPEP using anti-MIPEP antibody (A05926-1). MIPEP was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIPEP Antibody (A05926-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-ihc-testing-4.jpgAnti-MIPEP Antibody Picoband® IHC analysis of MIPEP using anti-MIPEP antibody (A05926-1). MIPEP was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIPEP Antibody (A05926-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-ihc-testing-5.jpgAnti-MIPEP Antibody Picoband® IHC analysis of MIPEP using anti-MIPEP antibody (A05926-1). MIPEP was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIPEP Antibody (A05926-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-ihc-testing-6.jpgAnti-MIPEP Antibody Picoband® IHC analysis of MIPEP using anti-MIPEP antibody (A05926-1). MIPEP was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIPEP Antibody (A05926-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-ihc-testing-7.jpgAnti-MIPEP Antibody Picoband® IHC analysis of MIPEP using anti-MIPEP antibody (A05926-1). MIPEP was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIPEP Antibody (A05926-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-ihc-testing-8.jpgAnti-MIPEP Antibody Picoband® IHC analysis of MIPEP using anti-MIPEP antibody (A05926-1). MIPEP was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIPEP Antibody (A05926-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05926-1-mipep-primary-antibodies-fcm-testing-9.pngAnti-MIPEP Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MIPEP antibody (A05926-1). Overlay histogram showing MCF-7 cells stained with A05926-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MIPEP Antibody (A05926-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mlkl-picoband-trade-antibody-a00535-3-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-wb-testing-1.jpgAnti-MLKL Antibody Picoband® Western blot analysis of MLKL using anti-MLKL antibody (A00535-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MLKL antigen affinity purified polyclonal antibody (Catalog # A00535-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MLKL at approximately 50 kDa. The expected band size for MLKL is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-ihc-testing-2.jpgAnti-MLKL Antibody Picoband® IHC analysis of MLKL using anti-MLKL antibody (A00535-3). MLKL was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLKL Antibody (A00535-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-ihc-testing-3.jpgAnti-MLKL Antibody Picoband® IHC analysis of MLKL using anti-MLKL antibody (A00535-3). MLKL was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLKL Antibody (A00535-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-ihc-testing-4.jpgAnti-MLKL Antibody Picoband® IHC analysis of MLKL using anti-MLKL antibody (A00535-3). MLKL was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLKL Antibody (A00535-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-ihc-testing-5.jpgAnti-MLKL Antibody Picoband® IHC analysis of MLKL using anti-MLKL antibody (A00535-3). MLKL was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLKL Antibody (A00535-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-ihc-testing-6.jpgAnti-MLKL Antibody Picoband® IHC analysis of MLKL using anti-MLKL antibody (A00535-3). MLKL was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLKL Antibody (A00535-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-ihc-testing-7.jpgAnti-MLKL Antibody Picoband® IHC analysis of MLKL using anti-MLKL antibody (A00535-3). MLKL was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MLKL Antibody (A00535-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-if-testing-8.jpgAnti-MLKL Antibody Picoband® IF analysis of MLKL using anti-MLKL antibody (A00535-3). MLKL was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MLKL Antibody (A00535-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00535-3-mlkl-primary-antibodies-fcm-testing-9.pngAnti-MLKL Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MLKL antibody (A00535-3). Overlay histogram showing MCF-7 cells stained with A00535-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MLKL Antibody (A00535-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-myo1g-picoband-trade-antibody-a08448-2-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08448-2-myo1g-primary-antibodies-wb-testing-1.jpgAnti-MYO1G Antibody Picoband® Western blot analysis of MYO1G using anti-MYO1G antibody (A08448-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYO1G antigen affinity purified polyclonal antibody (Catalog # A08448-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYO1G at approximately 116 kDa. The expected band size for MYO1G is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08448-2-myo1g-primary-antibodies-fcm-testing-2.pngAnti-MYO1G Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-MYO1G antibody (A08448-2). Overlay histogram showing HEL cells stained with A08448-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MYO1G Antibody (A08448-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcca-picoband-trade-antibody-a03395-1-boster.html2026-03-16T09:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-wb-testing-1.jpgAnti-PCCA Antibody Picoband® Western blot analysis of PCCA using anti-PCCA antibody (A03395-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCCA antigen affinity purified polyclonal antibody (Catalog # A03395-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCCA at approximately 70 kDa. The expected band size for PCCA is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-ihc-testing-2.jpgAnti-PCCA Antibody Picoband® IHC analysis of PCCA using anti-PCCA antibody (A03395-1). PCCA was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCCA Antibody (A03395-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-ihc-testing-3.jpgAnti-PCCA Antibody Picoband® IHC analysis of PCCA using anti-PCCA antibody (A03395-1). PCCA was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCCA Antibody (A03395-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-ihc-testing-4.jpgAnti-PCCA Antibody Picoband® IHC analysis of PCCA using anti-PCCA antibody (A03395-1). PCCA was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCCA Antibody (A03395-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-ihc-testing-5.jpgAnti-PCCA Antibody Picoband® IHC analysis of PCCA using anti-PCCA antibody (A03395-1). PCCA was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCCA Antibody (A03395-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-ihc-testing-6.jpgAnti-PCCA Antibody Picoband® IHC analysis of PCCA using anti-PCCA antibody (A03395-1). PCCA was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCCA Antibody (A03395-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-ihc-testing-7.jpgAnti-PCCA Antibody Picoband® IHC analysis of PCCA using anti-PCCA antibody (A03395-1). PCCA was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCCA Antibody (A03395-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-fcm-testing-8.pngAnti-PCCA Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PCCA antibody (A03395-1). Overlay histogram showing 293T cells stained with A03395-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PCCA Antibody (A03395-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03395-1-pcca-primary-antibodies-fcm-testing-9.pngAnti-PCCA Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PCCA antibody (A03395-1). Overlay histogram showing HepG2 cells stained with A03395-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PCCA Antibody (A03395-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pcdha12-picoband-trade-antibody-a15869-1-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15869-1-pcdha12-primary-antibodies-wb-testing-1.jpgAnti-PCDHA12 Antibody Picoband® Western blot analysis of PCDHA12 using anti-PCDHA12 antibody (A15869-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHA12 antigen affinity purified polyclonal antibody (Catalog # A15869-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHA12 at approximately 120 kDa. The expected band size for PCDHA12 is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15869-1-pcdha12-primary-antibodies-fcm-testing-2.pngAnti-PCDHA12 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-PCDHA12 antibody (A15869-1). Overlay histogram showing U20S cells stained with A15869-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHA12 Antibody (A15869-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pgbd4-picoband-trade-antibody-a19178-1-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19178-1-pgbd4-primary-antibodies-wb-testing-1.jpgAnti-PGBD4 Antibody Picoband® Western blot analysis of PGBD4 using anti-PGBD4 antibody (A19178-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: rat RH35 whole cell lysates, Lane 5: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGBD4 antigen affinity purified polyclonal antibody (Catalog # A19178-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGBD4 at approximately 70 kDa. The expected band size for PGBD4 is at 67 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-phf10-picoband-trade-antibody-a08195-1-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08195-1-phf10-primary-antibodies-wb-testing-1.jpgAnti-PHF10 Antibody Picoband® Western blot analysis of PHF10 using anti-PHF10 antibody (A08195-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF10 antigen affinity purified polyclonal antibody (Catalog # A08195-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHF10 at approximately 56 kDa. The expected band size for PHF10 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08195-1-phf10-primary-antibodies-fcm-testing-2.pngAnti-PHF10 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-PHF10 antibody (A08195-1). Overlay histogram showing K562 cells stained with A08195-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHF10 Antibody (A08195-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pla2g3-picoband-trade-antibody-a07886-1-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07886-1-pla2g3-primary-antibodies-wb-testing-1.jpgAnti-PLA2G3 Antibody Picoband® Western blot analysis of PLA2G3 using anti-PLA2G3 antibody (A07886-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLA2G3 antigen affinity purified polyclonal antibody (Catalog # A07886-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLA2G3 at approximately 65 kDa. The expected band size for PLA2G3 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07886-1-pla2g3-primary-antibodies-fcm-testing-2.pngAnti-PLA2G3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PLA2G3 antibody (A07886-1). Overlay histogram showing HepG2 cells stained with A07886-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PLA2G3 Antibody (A07886-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-plekhg4-picoband-trade-antibody-a10252-2-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10252-2-plekhg4-primary-antibodies-wb-testing-1.jpgAnti-PLEKHG4 Antibody Picoband® Western blot analysis of PLEKHG4 using anti-PLEKHG4 antibody (A10252-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLEKHG4 antigen affinity purified polyclonal antibody (Catalog # A10252-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLEKHG4 at approximately 140 kDa. The expected band size for PLEKHG4 is at 131 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10252-2-plekhg4-primary-antibodies-fcm-testing-2.pngAnti-PLEKHG4 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PLEKHG4 antibody (A10252-2). Overlay histogram showing SH-SY5Y cells stained with A10252-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PLEKHG4 Antibody (A10252-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-reck-picoband-trade-antibody-a06439-3-boster.html2026-03-16T09:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06439-3-reck-primary-antibodies-wb-testing-1.jpgAnti-RECK Antibody Picoband® Western blot analysis of RECK using anti-RECK antibody (A06439-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RECK antigen affinity purified polyclonal antibody (Catalog # A06439-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RECK at approximately 106 kDa. The expected band size for RECK is at 106 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06439-3-reck-primary-antibodies-fcm-testing-2.pngAnti-RECK Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-RECK antibody (A06439-3). Overlay histogram showing U251 cells stained with A06439-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RECK Antibody (A06439-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nf-kb-p65-rela-picoband-trade-antibody-a00284-4-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00284-4-rela-primary-antibodies-wb-testing-1.jpgAnti-NF-κB p65/RELA Antibody Picoband® Western blot analysis of NF-ΚB P6/RELA using anti-NF-ΚB P6/RELA antibody (A00284-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human Raji whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat C6 whole cell tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates, Lane 8: mouse Ana-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NF-ΚB P6/RELA antigen affinity purified polyclonal antibody (Catalog # A00284-4) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NF-ΚB P6/RELA at approximately 65 kDa. The expected band size for NF-ΚB P6/RELA is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00284-4-rela-primary-antibodies-fcm-testing-2.pngAnti-NF-κB p65/RELA Antibody Picoband® Flow Cytometry analysis of Daudi cells using anti-NF-ΚB P6/RELA antibody (A00284-4). Overlay histogram showing Daudi cells stained with A00284-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NF-ΚB P6/RELA Antibody (A00284-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-c16orf75-rmi2-picoband-trade-antibody-a08685-1-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08685-1-rmi2-primary-antibodies-wb-testing-1.jpgAnti-C16orf75/RMI2 Antibody Picoband® Western blot analysis of C16orf75/RMI2 using anti-C16orf75/RMI2 antibody (A08685-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HT-1080 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C16orf75/RMI2 antigen affinity purified polyclonal antibody (Catalog # A08685-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C16orf75/RMI2 at approximately 16 kDa. The expected band size for C16orf75/RMI2 is at 16 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-serpinb8-picoband-trade-antibody-a11265-1-boster.html2026-03-17T05:15:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11265-1-serpinb8-primary-antibodies-wb-testing-1.jpgAnti-SERPINB8 Antibody Picoband® Western blot analysis of SERPINB8 using anti-SERPINB8 antibody (A11265-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SERPINB8 antigen affinity purified polyclonal antibody (Catalog # A11265-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SERPINB8 at approximately 48 kDa. The expected band size for SERPINB8 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11265-1-serpinb8-primary-antibodies-if-testing-2.jpgAnti-SERPINB8 Antibody Picoband® IF analysis of SERPINB8 using anti-SERPINB8 antibody (A11265-1). SERPINB8 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SERPINB8 Antibody (A11265-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11265-1-serpinb8-primary-antibodies-fcm-testing-3.pngAnti-SERPINB8 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SERPINB8 antibody (A11265-1). Overlay histogram showing JK cells stained with A11265-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SERPINB8 Antibody (A11265-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-sh2d3c-picoband-trade-antibody-a04497-1-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04497-1-sh2d3c-primary-antibodies-wb-testing-1.jpgAnti-SH2D3C Antibody Picoband® Western blot analysis of SH2D3C using anti-SH2D3C antibody (A04497-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SH2D3C antigen affinity purified polyclonal antibody (Catalog # A04497-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SH2D3C at approximately 94 kDa. The expected band size for SH2D3C is at 94 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04497-1-sh2d3c-primary-antibodies-fcm-testing-2.pngAnti-SH2D3C Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-SH2D3C antibody (A04497-1). Overlay histogram showing HEL cells stained with A04497-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SH2D3C Antibody (A04497-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-shkbp1-picoband-trade-antibody-a14104-1-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-wb-testing-1.jpgAnti-SHKBP1 Antibody Picoband® Western blot analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHKBP1 antigen affinity purified polyclonal antibody (Catalog # A14104-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SHKBP1 at approximately 76 kDa. The expected band size for SHKBP1 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-2.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-3.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-4.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-5.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-6.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-7.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-8.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-ihc-testing-9.jpgAnti-SHKBP1 Antibody Picoband® IHC analysis of SHKBP1 using anti-SHKBP1 antibody (A14104-1). SHKBP1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHKBP1 Antibody (A14104-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14104-1-shkbp1-primary-antibodies-fcm-testing-10.pngAnti-SHKBP1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-SHKBP1 antibody (A14104-1). Overlay histogram showing A549 cells stained with A14104-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SHKBP1 Antibody (A14104-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-sim2-picoband-trade-antibody-a04436-2-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04436-2-sim2-primary-antibodies-wb-testing-1.jpgAnti-SIM2 Antibody Picoband® Western blot analysis of SIM2 using anti-SIM2 antibody (A04436-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: monkey COS-7 whole cell lysates, Lane 4: rat skeletal muscle tissue lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse skeletal muscle tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIM2 antigen affinity purified polyclonal antibody (Catalog # A04436-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SIM2 at approximately 65 kDa. The expected band size for SIM2 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04436-2-sim2-primary-antibodies-fcm-testing-2.pngAnti-SIM2 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-SIM2 antibody (A04436-2). Overlay histogram showing PC-3 cells stained with A04436-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SIM2 Antibody (A04436-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slain1-picoband-trade-antibody-a13403-2-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13403-2-slain1-primary-antibodies-wb-testing-1.jpgAnti-SLAIN1 Antibody Picoband® Western blot analysis of SLAIN1 using anti-SLAIN1 antibody (A13403-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLAIN1 antigen affinity purified polyclonal antibody (Catalog # A13403-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLAIN1 at approximately 70 kDa. The expected band size for SLAIN1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13403-2-slain1-primary-antibodies-fcm-testing-2.pngAnti-SLAIN1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SLAIN1 antibody (A13403-2). Overlay histogram showing JK cells stained with A13403-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SLAIN1 Antibody (A13403-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slamf6-picoband-trade-antibody-a05310-2-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05310-2-slamf6-primary-antibodies-wb-testing-1.jpgAnti-SLAMF6 Antibody Picoband® Western blot analysis of SLAMF6 using anti-SLAMF6 antibody (A05310-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Daudi whole cell lysates, Lane 2: human Ramos whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human MOLT-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLAMF6 antigen affinity purified polyclonal antibody (Catalog # A05310-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLAMF6 at approximately 60 kDa. The expected band size for SLAMF6 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05310-2-slamf6-primary-antibodies-fcm-testing-2.pngAnti-SLAMF6 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SLAMF6 antibody (A05310-2). Overlay histogram showing JK cells stained with A05310-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLAMF6 Antibody (A05310-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05310-2-slamf6-primary-antibodies-fcm-testing-3.pngAnti-SLAMF6 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-SLAMF6 antibody (A05310-2). Overlay histogram showing THP-1 cells stained with A05310-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLAMF6 Antibody (A05310-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slc13a4-picoband-trade-antibody-a13300-1-boster.html2026-03-16T09:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13300-1-slc13a4-primary-antibodies-wb-testing-1.jpgAnti-SLC13A4 Antibody Picoband® Western blot analysis of SLC13A4 using anti-SLC13A4 antibody (A16132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse testis tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC13A4 antigen affinity purified polyclonal antibody (Catalog # A16132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC13A4 at approximately 62 kDa. The expected band size for SLC13A4 is at 69 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-slc22a10-picoband-trade-antibody-a15610-1-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15610-1-slc22a10-primary-antibodies-wb-testing-1_1.jpgAnti-SLC22A10 Antibody Picoband® Western blot analysis of SLC22A10 using anti-SLC22A10 antibody (A15610-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC22A10 antigen affinity purified polyclonal antibody (Catalog # A15610-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC22A10 at approximately 36 kDa. The expected band size for SLC22A10 is at 30, 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15610-1-slc22a10-primary-antibodies-fcm-testing-2.pngAnti-SLC22A10 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-SLC22A10 antibody (A15610-1). Overlay histogram showing 293T cells stained with A15610-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC22A10 Antibody (A15610-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slc25a25-picoband-trade-antibody-a09109-1-boster.html2026-03-16T09:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09109-1-slc25a5-primary-antibodies-wb-testing-1.jpgAnti-SLC25A25 Antibody Picoband® Western blot analysis of SLC25A25 using anti-SLC25A25 antibody (A09109-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC25A25 antigen affinity purified polyclonal antibody (Catalog # A09109-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC25A25 at approximately 50-55 kDa. The expected band size for SLC25A25 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09109-1-slc25a5-primary-antibodies-ihc-testing-2.jpgAnti-SLC25A25 Antibody Picoband® IHC analysis of SLC25A25 using anti-SLC25A25 antibody (A09109-1). SLC25A25 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC25A25 Antibody (A09109-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09109-1-slc25a5-primary-antibodies-ihc-testing-3.jpgAnti-SLC25A25 Antibody Picoband® IHC analysis of SLC25A25 using anti-SLC25A25 antibody (A09109-1). SLC25A25 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC25A25 Antibody (A09109-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09109-1-slc25a5-primary-antibodies-fcm-testing-4.pngAnti-SLC25A25 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SLC25A25 antibody (A09109-1). Overlay histogram showing JK cells stained with A09109-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC25A25 Antibody (A09109-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slc26a9-picoband-trade-antibody-a07581-1-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07581-1-slc26a9-primary-antibodies-wb-testing-1.jpgAnti-SLC26A9 Antibody Picoband® Western blot analysis of SLC26A9 using anti-SLC26A9 antibody (A07581-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat stomach tissue lysates, Lane 3: rat lung tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse stomach tissue lysates, Lane 6: mouse lung tissue lysates, Lane 7: mouse MFC whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC26A9 antigen affinity purified polyclonal antibody (Catalog # A07581-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC26A9 at approximately 90 kDa. The expected band size for SLC26A9 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07581-1-slc26a9-primary-antibodies-fcm-testing-2.pngAnti-SLC26A9 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-SLC26A9 antibody (A07581-1). Overlay histogram showing HepG2 cells stained with A07581-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC26A9 Antibody (A07581-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (A07581-1, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slc37a3-picoband-trade-antibody-a14532-1-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14532-1-slc37a3-primary-antibodies-wb-testing-1_1.jpgAnti-SLC37A3 Antibody Picoband®Western blot analysis of SLC37A3 using anti-SLC37A3 antibody (A14532-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC37A3 antigen affinity purified polyclonal antibody (A14532-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC37A3 at approximately 54 kDa. The expected band size for SLC37A3 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14532-1-slc37a3-primary-antibodies-if-testing-2.jpgAnti-SLC37A3 Antibody Picoband® IF analysis of SLC37A3 using anti-SLC37A3 antibody (A14532-1). SLC37A3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SLC37A3 Antibody (A14532-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14532-1-slc37a3-primary-antibodies-fcm-testing-3.pngAnti-SLC37A3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-SLC37A3 antibody (A14532-1). Overlay histogram showing U251 cells stained with A14532-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC37A3 Antibody (A14532-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slc39a10-picoband-trade-antibody-a09043-1-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-wb-testing-1_1.jpgAnti-SLC39A10 Antibody Picoband®Western blot analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC39A10 antigen affinity purified polyclonal antibody (A09043-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLC39A10 at approximately 95-100 kDa. The expected band size for SLC39A10 is at 94 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-ihc-testing-1.jpgAnti-SLC39A10 Antibody Picoband®IHC analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in a paraffin-embedded section of human brest cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-ihc-testing-2.jpgAnti-SLC39A10 Antibody Picoband®IHC analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-ihc-testing-3.jpgAnti-SLC39A10 Antibody Picoband®IHC analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in a paraffin-embedded section of mouse brain tissue tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-ihc-testing-4.jpgAnti-SLC39A10 Antibody Picoband®IHC analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in a paraffin-embedded section of rat brain tissue tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-if-testing-1.jpgAnti-SLC39A10 Antibody Picoband®IF analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-if-testing-2.jpgAnti-SLC39A10 Antibody Picoband®IF analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-if-testing-3.jpgAnti-SLC39A10 Antibody Picoband®IF analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-if-testing-4.jpgAnti-SLC39A10 Antibody Picoband®IF analysis of SLC39A10 using anti-SLC39A10 antibody (A09043-1). SLC39A10 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SLC39A10 Antibody (A09043-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09043-1-slc39a10-primary-antibodies-fcm-testing-1.jpgAnti-SLC39A10 Antibody Picoband®Flow Cytometry analysis of CACO-2 cells using anti-SLC39A10 antibody (A09043-1). Overlay histogram showing CACO-2 cells stained with A09043-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC39A10 Antibody (A09043-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-gat1-slc6a1-picoband-trade-antibody-a05109-2-boster.html2026-03-16T09:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05109-2-slc6a1-primary-antibodies-wb-testing-1.jpgAnti-GAT1/SLC6A1 Antibody Picoband® Western blot analysis of GAT1/SLC6A1 using anti-GAT1/SLC6A1 antibody (A05109-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAT1/SLC6A1 antigen affinity purified polyclonal antibody (Catalog # A05109-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAT1/SLC6A1 at approximately 67 kDa. The expected band size for GAT1/SLC6A1 is at 67 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-slc6a20-picoband-trade-antibody-a09824-1-boster.html2026-03-16T09:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-wb-testing-1.jpgAnti-SLC6A20 Antibody Picoband® Western blot analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human CCRF-CEM whole cell lysates, Lane 2: human COLO 320 whole cell lysates, Lane 3: human SW620 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC6A20 antigen affinity purified polyclonal antibody (Catalog # A09824-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC6A20 at approximately 70 kDa. The expected band size for SLC6A20 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-2.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-3.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-4.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-5.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-6.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-7.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-8.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-9.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-10.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-11.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-12.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-ihc-testing-13.jpgAnti-SLC6A20 Antibody Picoband® IHC analysis of SLC6A20 using anti-SLC6A20 antibody (A09824-1). SLC6A20 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC6A20 Antibody (A09824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09824-1-slc6a20-primary-antibodies-fcm-testing-14.pngAnti-SLC6A20 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-SLC6A20 antibody (A09824-1). Overlay histogram showing 293T cells stained with A09824-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLC6A20 Antibody (A09824-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slfn13-picoband-trade-antibody-a17269-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17269-slfn13-primary-antibodies-wb-testing-1_1.jpgAnti-SLFN13 Antibody Picoband®Western blot analysis of SLFN13 using anti-SLFN13 antibody (A17269). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse C2C12 whole cell lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLFN13 antigen affinity purified polyclonal antibody (A17269) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SLFN13 at approximately 102 kDa. The expected band size for SLFN13 is at 102 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-slitrk1-picoband-trade-antibody-a07507-2-boster.html2026-03-17T05:15:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07507-2-slitrk1-primary-antibodies-wb-testing-1.jpgAnti-SLITRK1 Antibody Picoband® Western blot analysis of SLITRK1 using anti-SLITRK1 antibody (A07507-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLITRK1 antigen affinity purified polyclonal antibody (Catalog # A07507-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLITRK1 at approximately 55 kDa. The expected band size for SLITRK1 is at 78 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07507-2-slitrk1-primary-antibodies-fcm-testing-2.pngAnti-SLITRK1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-SLITRK1 antibody (A07507-2). Overlay histogram showing U251 cells stained with A07507-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SLITRK1 Antibody (A07507-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-slk-picoband-trade-antibody-a01614-2-boster.html2026-03-16T09:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-wb-testing-1.jpgAnti-SLK Antibody Picoband® Western blot analysis of SLK using anti-SLK antibody (A01614-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLK antigen affinity purified polyclonal antibody (Catalog # A01614-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLK at approximately 245 kDa. The expected band size for SLK is at 143 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-2.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-3.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-4.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-5.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-6.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-7.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-8.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-ihc-testing-9.jpgAnti-SLK Antibody Picoband® IHC analysis of SLK using anti-SLK antibody (A01614-2). SLK was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLK Antibody (A01614-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01614-2-slk-primary-antibodies-fcm-testing-10.pngAnti-SLK Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-SLK antibody (A01614-2). Overlay histogram showing A549 cells stained with A01614-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SLK Antibody (A01614-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-smtnl2-picoband-trade-antibody-a18269-1-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18269-1-smtnl2-primary-antibodies-wb-testing-1.jpgAnti-SMTNL2 Antibody Picoband® Western blot analysis of SMTNL2 using anti-SMTNL2 antibody (A18269-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human COLO 320 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMTNL2 antigen affinity purified polyclonal antibody (Catalog # A18269-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SMTNL2 at approximately 50 kDa. The expected band size for SMTNL2 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18269-1-smtnl2-primary-antibodies-if-testing-2.jpgAnti-SMTNL2 Antibody Picoband® IF analysis of SMTNL2 using anti-SMTNL2 antibody (A18269-1). SMTNL2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SMTNL2 Antibody (A18269-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18269-1-smtnl2-primary-antibodies-fcm-testing-3.pngAnti-SMTNL2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-SMTNL2 antibody (A18269-1). Overlay histogram showing MCF-7 cells stained with A18269-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SMTNL2 Antibody (A18269-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-snrnp70-picoband-trade-antibody-a03527-2-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03527-2-snrnp70-primary-antibodies-wb-testing-1.jpgAnti-SNRNP70 Antibody Picoband® Western blot analysis of SNRNP70 using anti-SNRNP70 antibody (A03527-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNRNP70 antigen affinity purified polyclonal antibody (Catalog # A03527-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SNRNP70 at approximately 95 kDa. The expected band size for SNRNP70 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03527-2-snrnp70-primary-antibodies-ihc-testing-2.jpgAnti-SNRNP70 Antibody Picoband® IHC analysis of SNRNP70 using anti-SNRNP70 antibody (A03527-2). SNRNP70 was detected in a paraffin-embedded section of rat brain(Cerebral cortex) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SNRNP70 Antibody (A03527-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03527-2-snrnp70-primary-antibodies-ihc-testing-3.jpgAnti-SNRNP70 Antibody Picoband® IHC analysis of SNRNP70 using anti-SNRNP70 antibody (A03527-2). SNRNP70 was detected in a paraffin-embedded section of rat brain(Cerebral cortex) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SNRNP70 Antibody (A03527-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03527-2-snrnp70-primary-antibodies-ihc-testing-4.jpgAnti-SNRNP70 Antibody Picoband® IHC analysis of SNRNP70 using anti-SNRNP70 antibody (A03527-2). SNRNP70 was detected in a paraffin-embedded section of rat brain(Midbrain) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SNRNP70 Antibody (A03527-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03527-2-snrnp70-primary-antibodies-ihc-testing-5.jpgAnti-SNRNP70 Antibody Picoband® IHC analysis of SNRNP70 using anti-SNRNP70 antibody (A03527-2). SNRNP70 was detected in a paraffin-embedded section of rat brain(Midbrain) tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SNRNP70 Antibody (A03527-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03527-2-snrnp70-primary-antibodies-if-testing-6.jpgAnti-SNRNP70 Antibody Picoband® IF analysis of SNRNP70 using anti-SNRNP70 antibody (A03527-2) and anti-Beta Tubulin antibody (M01857-3). SNRNP70 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SNRNP70 Antibody (A03527-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03527-2-snrnp70-primary-antibodies-fcm-testing-7.pngAnti-SNRNP70 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-SNRNP70 antibody (A03527-2). Overlay histogram showing HepG2 cells stained with A03527-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SNRNP70 Antibody (A03527-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stim1-picoband-trade-antibody-a00312-1-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-wb-testing-1.jpgAnti-STIM1 Antibody Picoband® Western blot analysis of STIM1 using anti-STIM1 antibody (A00312-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STIM1 antigen affinity purified polyclonal antibody (Catalog # A00312-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STIM1 at approximately 85 kDa. The expected band size for STIM1 is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-2.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-3.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-4.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-5.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-6.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-7.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-8.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-ihc-testing-9.jpgAnti-STIM1 Antibody Picoband® IHC analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-fcm-testing-10.pngAnti-STIM1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-STIM1 antibody (A00312-1). Overlay histogram showing K562 cells stained with A00312-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STIM1 Antibody (A00312-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-if-testing-11.jpgAnti-STIM1 Antibody Picoband® IF analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-if-testing-12.jpgAnti-STIM1 Antibody Picoband® IF analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00312-1-stim1-primary-antibodies-if-testing-13.jpgAnti-STIM1 Antibody Picoband® IF analysis of STIM1 using anti-STIM1 antibody (A00312-1). STIM1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-STIM1 Antibody (A00312-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-tfpi2-picoband-trade-antibody-a03697-2-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03697-2-tfip2-primary-antibodies-wb-testing-1.jpgAnti-TFPI2 Antibody Picoband® Western blot analysis of TFPI2 using anti-TFPI2 antibody (A03697-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates, Lane 2: rat RH-35 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFPI2 antigen affinity purified polyclonal antibody (Catalog # A03697-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFPI2 at approximately 30 kDa. The expected band size for TFPI2 is at 27 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-tenascin-r-tnr-picoband-trade-antibody-a04810-1-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04810-1-tnr-primary-antibodies-wb-testing-1.jpgAnti-Tenascin-R/TNR Antibody Picoband® Western blot analysis of Tenascin-R/TNR using anti-Tenascin-R/TNR antibody (A04810-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tenascin-R/TNR antigen affinity purified polyclonal antibody (Catalog # A04810-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tenascin-R/TNR at approximately 180 kDa. The expected band size for Tenascin-R/TNR is at 150 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-tnrc6c-picoband-trade-antibody-a09089-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09089-tnrc6c-primary-antibodies-wb-testing-1.jpgAnti-TNRC6C Antibody Picoband® Western blot analysis of TNRC6C using anti-TNRC6C antibody (A09089). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNRC6C antigen affinity purified polyclonal antibody (Catalog # A09089) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TNRC6C at approximately 176-200 kDa. The expected band size for TNRC6C is at 176 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09089-tnrc6c-primary-antibodies-fcm-testing-2.pngAnti-TNRC6C Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-TNRC6C antibody (A09089). Overlay histogram showing U251 cells stained with A09089 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TNRC6C Antibody (A09089, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-erbb4-picoband-trade-antibody-a00296-1-boster.html2026-03-16T09:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-wb-testing-1.jpgAnti-ERBB4 Antibody Picoband® Western blot analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ERBB4 antigen affinity purified polyclonal antibody (Catalog # A00296-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ERBB4 at approximately 180 kDa. The expected band size for ERBB4 is at 147 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-2.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-3.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-4.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-5.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human pancreas ductal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-6.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-7.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-8.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00296-1-erbb4-primary-antibodies-ihc-testing-9.jpgAnti-ERBB4 Antibody Picoband® IHC analysis of ERBB4 using anti-ERBB4 antibody (A00296-1). ERBB4 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERBB4 Antibody (A00296-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-wnt5a-picoband-trade-antibody-a00549-1-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00549-1-wnt5a-primary-antibodies-wb-testing-1.jpgAnti-WNT5A Antibody Picoband® Western blot analysis of WNT5A using anti-WNT5A antibody (A00549-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-WNT5A antigen affinity purified polyclonal antibody (Catalog # A00549-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for WNT5A at approximately 43 kDa. The expected band size for WNT5A is at 42 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-apc1-anapc1-picoband-trade-antibody-a03471-2-boster.html2026-03-17T05:15:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03471-2-anapc1-primary-antibodies-wb-testing-1.jpgAnti-APC1/ANAPC1 Antibody Picoband® Western blot analysis of APC1/ANAPC1 using anti-APC1/ANAPC1 antibody (A03471-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEK293 whole cell lysates, Lane 2: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APC1/ANAPC1 antigen affinity purified polyclonal antibody (Catalog # A03471-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for APC1/ANAPC1 at approximately 240 kDa. The expected band size for APC1/ANAPC1 is at 217 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03471-2-anapc1-primary-antibodies-ihc-testing-2.jpgAnti-APC1/ANAPC1 Antibody Picoband® IHC analysis of APC1/ANAPC1 using anti-APC1/ANAPC1 antibody (A03471-2). APC1/ANAPC1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APC1/ANAPC1 Antibody (A03471-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03471-2-anapc1-primary-antibodies-if-testing-3.jpgAnti-APC1/ANAPC1 Antibody Picoband® IF analysis of APC1/ANAPC1 using anti-APC1/ANAPC1 antibody (A03471-2). APC1/ANAPC1 was detected in an immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-APC1/ANAPC1 Antibody (A03471-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03471-2-anapc1-primary-antibodies-fcm-testing-4.pngAnti-APC1/ANAPC1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-APC1/ANAPC1 antibody (A03471-2). Overlay histogram showing A549 cells stained with A03471-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-APC1/ANAPC1 Antibody (A03471-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-aspergillus-nidulans-ania-01953-dz41468-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-aspergillus-nidulans-ania-03185-dz41470-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-parasteatoda-tepidariorum-hairy-dz41480-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-tea-dz41489-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-g6p-dz41490-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-g6p-dz41491-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-elovl7-dz41492-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-gba1-dz41494-boster.html2026-03-10T04:36:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-strongyloides-ratti-metalloendopeptidase-dz41495-boster.html2026-03-10T04:37:00+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-2w1s-dz41496-boster.html2026-03-10T04:37:00+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-anopheles-stephensi-5-hydroxytryptamine-receptor-1-like-transcript-variant-x1-dz41499-boster.html2026-03-10T04:37:00+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-yippee-dz41501-boster.html2026-03-10T04:37:00+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-tea-dz41504-boster.html2026-03-10T04:37:00+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-adam2-picoband-trade-antibody-a08379-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08379-2-adam2-primary-antibodies-wb-testing-1.jpgAnti-ADAM2 Antibody Picoband® Western blot analysis of ADAM2 using anti-ADAM2 antibody (A08379-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADAM2 antigen affinity purified polyclonal antibody (Catalog # A08379-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADAM2 at approximately 69 kDa. The expected band size for ADAM2 is at 82 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08379-2-adam2-primary-antibodies-fcm-testing-2.pngAnti-ADAM2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-ADAM2 antibody (A08379-2). Overlay histogram showing MCF-7 cells stained with A08379-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ADAM2 Antibody (A08379-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rpe-picoband-trade-antibody-a05272-1-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05272-1-rpe-primary-antibodies-wb-testing-1_1.jpgAnti-RPE Antibody Picoband®Western blot analysis of RPE using anti-RPE antibody (A05272-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPE antigen affinity purified polyclonal antibody (Catalog # A05272-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPE at approximately 25 kDa. The expected band size for RPE is at 25 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-bestrophin-1-best1-picoband-trade-antibody-a01434-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01434-2-best1-primary-antibodies-wb-testing-1.jpgAnti-Bestrophin-1/Best1 Antibody Picoband® Western blot analysis of Bestrophin-1/Best1 Antibody using anti-Bestrophin-1/Best1 Antibody antibody (A01434-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse eye tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bestrophin-1/Best1 Antibody antigen affinity purified polyclonal antibody (Catalog # A01434-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bestrophin-1/Best1 Antibody at approximately 56,60 kDa. The expected band size for Bestrophin-1/Best1 Antibody is at 64 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-lmo2-picoband-trade-antibody-a03502-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03502-2-lmo2-primary-antibodies-wb-testing-1.jpgAnti-LMO2 Antibody Picoband® Western blot analysis of LMO2 using anti-LMO2 antibody (A03502-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMO2 antigen affinity purified polyclonal antibody (Catalog # A03502-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LMO2 at approximately 22 kDa. The expected band size for LMO2 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03502-2-lmo2-primary-antibodies-ip-testing-1.jpgAnti-LMO2 Antibody Picoband®Immunoprecipitating (IP) LMO2 in K562 whole cell lysate. Western blot analysis of LMO2 using anti-LMO2 antibody (A03502-2); Lane 1: K562 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-LMO2 antibody in K562 whole cell lysate; Lane 3: anti-LMO2 antibody (2μg) + K562 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-LMO2 antigen affinity purified polyclonal antibody (A03502-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for LMO2 at approximately 22 kDa. The expected band size for LMO2 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03502-2-lmo2-primary-antibodies-fcm-testing-2.pngAnti-LMO2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-LMO2 antibody (A03502-2). Overlay histogram showing K562 cells stained with A03502-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LMO2 Antibody (A03502-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-cd63-picoband-trade-antibody-a01080-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01080-2-cd63-primary-antibodies-wb-testing-1.jpgAnti-Cd63 Antibody Picoband® Western blot analysis of Cd63 using anti-Cd63 antibody (A01080-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat lung tissue lysates, Lane 2: rat PC-12 whole cell lysates, Lane 3: rat RH35 whole cell lysates, Lane 4: mouse lung tissue lysates, Lane 5: mouse RAW264.7 whole cell lysates, Lane 6: mouse ANA-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cd63 antigen affinity purified polyclonal antibody (Catalog # A01080-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cd63 at approximately 60 kDa. The expected band size for Cd63 is at 26 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-herp-herpud1-picoband-trade-antibody-a04908-2-boster.html2026-03-16T09:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-wb-testing-1.jpgAnti-HERP/HERPUD1 Antibody Picoband® Western blot analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human LNCAP whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HERP/HERPUD1 antigen affinity purified polyclonal antibody (Catalog # A04908-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HERP/HERPUD1 at approximately 56 kDa. The expected band size for HERP/HERPUD1 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-2.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-3.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-4.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-5.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-6.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-7.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-8.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-9.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-10.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-11.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-12.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-ihc-testing-13.jpgAnti-HERP/HERPUD1 Antibody Picoband® IHC analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-if-testing-14.jpgAnti-HERP/HERPUD1 Antibody Picoband® IF analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-if-testing-15.jpgAnti-HERP/HERPUD1 Antibody Picoband® IF analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04908-2-herpud1-primary-antibodies-if-testing-16.jpgAnti-HERP/HERPUD1 Antibody Picoband® IF analysis of HERP/HERPUD1 using anti-HERP/HERPUD1 antibody (A04908-2). HERP/HERPUD1 was detected in a paraffin-embedded section of human ovarian tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HERP/HERPUD1 Antibody (A04908-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-tnik-picoband-trade-antibody-a03934-3-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-wb-testing-1.jpgAnti-TNIK Antibody Picoband® Western blot analysis of TNIK using anti-TNIK antibody (A03934-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNIK antigen affinity purified polyclonal antibody (Catalog # A03934-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TNIK at approximately 180,150 kDa. The expected band size for TNIK is at 155 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-2.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-3.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-4.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-5.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-6.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-7.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-8.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-9.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-10.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-11.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-12.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-ihc-testing-13.jpgAnti-TNIK Antibody Picoband® IHC analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-if-testing-14.jpgAnti-TNIK Antibody Picoband® IF analysis of TNIK using anti-TNIK antibody (A03934-3). TNIK was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TNIK Antibody (A03934-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03934-3-tnik-primary-antibodies-fcm-testing-15.pngAnti-TNIK Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-TNIK antibody (A03934-3). Overlay histogram showing K562 cells stained with A03934-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TNIK Antibody (A03934-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nup88-picoband-trade-antibody-a05382-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05382-2-nup88-primary-antibodies-wb-testing-1.jpgAnti-NUP88 Antibody Picoband® Western blot analysis of NUP88 using anti-NUP88 antibody (A05382-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP88 antigen affinity purified polyclonal antibody (Catalog # A05382-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP88 at approximately 84 kDa. The expected band size for NUP88 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05382-2-nup88-primary-antibodies-if-testing-2.jpgAnti-NUP88 Antibody Picoband® IF analysis of NUP88 using anti-NUP88 antibody (A05382-2) and anti-Beta Tubulin antibody (M01857-3). NUP88 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP88 Antibody (A05382-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-ints4-picoband-trade-antibody-a13277-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13277-2-ints4-primary-antibodies-wb-testing-1.jpgAnti-INTS4 Antibody Picoband® Western blot analysis of INTS4 using anti-INTS4 antibody (A13277-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INTS4 antigen affinity purified polyclonal antibody (Catalog # A13277-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INTS4 at approximately 140 kDa. The expected band size for INTS4 is at 108 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13277-2-ints4-primary-antibodies-ihc-testing-2.jpgAnti-INTS4 Antibody Picoband® IHC analysis of INTS4 using anti-INTS4 antibody (A13277-2). INTS4 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INTS4 Antibody (A13277-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13277-2-ints4-primary-antibodies-ihc-testing-3.jpgAnti-INTS4 Antibody Picoband® IHC analysis of INTS4 using anti-INTS4 antibody (A13277-2). INTS4 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-INTS4 Antibody (A13277-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13277-2-ints4-primary-antibodies-fcm-testing-4.pngAnti-INTS4 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-INTS4 antibody (A13277-2). Overlay histogram showing MCF-7 cells stained with A13277-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-INTS4 Antibody (A13277-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-coq8b-picoband-trade-antibody-a32263-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-wb-testing-1.jpgAnti-COQ8B Antibody Picoband® Western blot analysis of COQ8B using anti-COQ8B antibody (A32263-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat stomach tissue lysates, Lane 6: rat thymus tissue lysates, Lane 7: mouse stomach tissue lysates, Lane 8: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-COQ8B antigen affinity purified polyclonal antibody (Catalog # A32263-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for COQ8B at approximately 65 kDa. The expected band size for COQ8B is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-2.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-3.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-4.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-5.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-6.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-7.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-8.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-9.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-10.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-ihc-testing-11.jpgAnti-COQ8B Antibody Picoband® IHC analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-if-testing-12.jpgAnti-COQ8B Antibody Picoband® IF analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-if-testing-13.jpgAnti-COQ8B Antibody Picoband® IF analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1141) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32263-2-coq8b-primary-antibodies-if-testing-14.jpgAnti-COQ8B Antibody Picoband® IF analysis of COQ8B using anti-COQ8B antibody (A32263-2). COQ8B was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-COQ8B Antibody (A32263-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1141) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-stanniocalcin-2-stc2-picoband-trade-antibody-a05017-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-wb-testing-1.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® Western blot analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Stanniocalcin 2/STC2 antigen affinity purified polyclonal antibody (Catalog # A05017) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Stanniocalcin 2/STC2 at approximately 33 kDa. The expected band size for Stanniocalcin 2/STC2 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-2.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-3.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-4.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-5.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-6.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-7.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-8.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-9.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-10.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-ihc-testing-11.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IHC analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-if-testing-12.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IF analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-fcm-testing-13.pngAnti-Stanniocalcin 2/STC2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-Stanniocalcin 2/STC2 antibody (A05017). Overlay histogram showing MCF-7 cells stained with A05017 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-if-testing-14.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IF analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05017-stc2-primary-antibodies-if-testing-15.jpgAnti-Stanniocalcin 2/STC2 Antibody Picoband® IF analysis of Stanniocalcin 2/STC2 using anti-Stanniocalcin 2/STC2 antibody (A05017). Stanniocalcin 2/STC2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Stanniocalcin 2/STC2 Antibody (A05017) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-nkd1-picoband-trade-antibody-a06747-1-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06747-1-nkd1-primary-antibodies-wb-testing-1.jpgAnti-NKD1 Antibody Picoband® Western blot analysis of NKD1 using anti-NKD1 antibody (A06747-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SW620 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NKD1 antigen affinity purified polyclonal antibody (Catalog # A06747-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NKD1 at approximately 52 kDa. The expected band size for NKD1 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06747-1-nkd1-primary-antibodies-fcm-testing-2.pngAnti-NKD1 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-NKD1 antibody (A06747-1). Overlay histogram showing Caco-2 cells stained with A06747-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NKD1 Antibody (A06747-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-bche-picoband-trade-antibody-a00258-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00258-2-bche-primary-antibodies-wb-testing-1.jpgAnti-BCHE Antibody Picoband® Western blot analysis of BCHE using anti-BCHE antibody (A00258-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCHE antigen affinity purified polyclonal antibody (Catalog # A00258-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCHE at approximately 85-90 kDa. The expected band size for BCHE is at 68 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-angptl4-picoband-trade-antibody-a01147-3-boster.html2026-03-16T09:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01147-3-angptl4-primary-antibodies-wb-testing-1.jpgAnti-ANGPTL4 Antibody Picoband® Western blot analysis of ANGPTL4 using anti-ANGPTL4 antibody (A01147-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SW620 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANGPTL4 antigen affinity purified polyclonal antibody (Catalog # A01147-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ANGPTL4 at approximately 40-50 kDa. The expected band size for ANGPTL4 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01147-3-angptl4-primary-antibodies-fcm-testing-2.pngAnti-ANGPTL4 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-ANGPTL4 antibody (A01147-3). Overlay histogram showing 293T cells stained with A01147-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ANGPTL4 Antibody (A01147-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-axin1-picoband-trade-antibody-a00986-2-boster.html2026-03-17T05:15:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00986-2-axin1-primary-antibodies-wb-testing-1.jpgAnti-AXIN1 Antibody Picoband® Western blot analysis of AXIN1 using anti-AXIN1 antibody (A00986-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HT-1080 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AXIN1 antigen affinity purified polyclonal antibody (Catalog # A00986-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AXIN1 at approximately 96,96-110 kDa. The expected band size for AXIN1 is at 96 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00986-2-axin1-primary-antibodies-if-testing-2.jpgAnti-AXIN1 Antibody Picoband® IF analysis of AXIN1 using anti-AXIN1 antibody (A00986-2) and anti-Beta Tubulin antibody (M01857-3). AXIN1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-AXIN1 Antibody (A00986-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-cd21-cr2-picoband-trade-antibody-a01632-5-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01632-5-cd21-primary-antibodies-wb-testing-1.jpgAnti-CD21/CR2 Antibody Picoband® Western blot analysis of CD21/CR2 using anti-CD21/CR2 antibody (A01632-5). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse Raw264.7 whole cell lysates, Lane 2: mouse Ana-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD21/CR2 antigen affinity purified polyclonal antibody (Catalog # A01632-5) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD21/CR2 at approximately 100,150 kDa. The expected band size for CD21/CR2 is at 113 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-tfb2m-picoband-trade-antibody-a05679-2-boster.html2026-03-16T09:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05679-2-tfb2m-primary-antibodies-wb-testing-1.jpgAnti-TFB2M Antibody Picoband® Western blot analysis of TFB2M using anti-TFB2M antibody (A05679-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TFB2M antigen affinity purified polyclonal antibody (Catalog # A05679-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TFB2M at approximately 38 kDa. The expected band size for TFB2M is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05679-2-tfb2m-primary-antibodies-fcm-testing-2.pngAnti-TFB2M Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-TFB2M antibody (A05679-2). Overlay histogram showing K562 cells stained with A05679-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TFB2M Antibody (A05679-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-samd9l-picoband-trade-antibody-a12350-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-wb-testing-1.jpgAnti-SAMD9L Antibody Picoband® Western blot analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SAMD9L antigen affinity purified polyclonal antibody (Catalog # A12350-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SAMD9L at approximately 200 kDa. The expected band size for SAMD9L is at 185 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-2.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-3.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-4.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-5.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-6.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-7.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-8.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-9.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-10.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-11.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-12.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-13.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-14.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-ihc-testing-15.jpgAnti-SAMD9L Antibody Picoband® IHC analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-if-testing-16.jpgAnti-SAMD9L Antibody Picoband® IF analysis of SAMD9L using anti-SAMD9L antibody (A12350-1). SAMD9L was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SAMD9L Antibody (A12350-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1141) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12350-1-samd9l-primary-antibodies-fcm-testing-17.pngAnti-SAMD9L Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-SAMD9L antibody (A12350-1). Overlay histogram showing U251 cells stained with A12350-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SAMD9L Antibody (A12350-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-sass6-picoband-trade-antibody-a05762-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-wb-testing-1.jpgAnti-SASS6 Antibody Picoband® Western blot analysis of SASS6 using anti-SASS6 antibody (A05762-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SASS6 antigen affinity purified polyclonal antibody (Catalog # A05762-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SASS6 at approximately 74,70-74 kDa. The expected band size for SASS6 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-2.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-3.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-4.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-5.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-6.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-7.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-8.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-9.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-10.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-11.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-12.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-ihc-testing-13.jpgAnti-SASS6 Antibody Picoband® IHC analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-if-testing-14.jpgAnti-SASS6 Antibody Picoband® IF analysis of SASS6 using anti-SASS6 antibody (A05762-1). SASS6 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SASS6 Antibody (A05762-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05762-1-sass6-primary-antibodies-fcm-testing-15.pngAnti-SASS6 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-SASS6 antibody (A05762-1). Overlay histogram showing MCF-7 cells stained with A05762-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SASS6 Antibody (A05762-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-scamp3-picoband-trade-antibody-a08215-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-wb-testing-1.jpgAnti-SCAMP3 Antibody Picoband® Western blot analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HUH-7 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCAMP3 antigen affinity purified polyclonal antibody (Catalog # A08215-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SCAMP3 at approximately 36 kDa. The expected band size for SCAMP3 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-2.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-3.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human appendiceal carcinoid tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-4.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-5.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-6.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-7.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-8.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-9.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-10.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-11.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-12.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-13.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-14.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-ihc-testing-15.jpgAnti-SCAMP3 Antibody Picoband® IHC analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-if-testing-16.jpgAnti-SCAMP3 Antibody Picoband® IF analysis of SCAMP3 using anti-SCAMP3 antibody (A08215-1). SCAMP3 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SCAMP3 Antibody (A08215-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08215-1-scamp3-primary-antibodies-fcm-testing-17.pngAnti-SCAMP3 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-SCAMP3 antibody (A08215-1). Overlay histogram showing 293T cells stained with A08215-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SCAMP3 Antibody (A08215-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-sclt1-picoband-trade-antibody-a11417-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11417-1-sclt1-primary-antibodies-wb-testing-1.jpgAnti-SCLT1 Antibody Picoband® Western blot analysis of SCLT1 using anti-SCLT1 antibody (A11417-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human COLO320 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCLT1 antigen affinity purified polyclonal antibody (Catalog # A11417-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SCLT1 at approximately 75 kDa. The expected band size for SCLT1 is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11417-1-sclt1-primary-antibodies-fcm-testing-2.pngAnti-SCLT1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-SCLT1 antibody (A11417-1). Overlay histogram showing 293T cells stained with A11417-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SCLT1 Antibody (A11417-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-scml2-picoband-trade-antibody-a08958-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08958-1-scml2-primary-antibodies-wb-testing-1.jpgAnti-SCML2 Antibody Picoband® Western blot analysis of SCML2 using anti-SCML2 antibody (A08958-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCML2 antigen affinity purified polyclonal antibody (Catalog # A08958-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SCML2 at approximately 85 kDa. The expected band size for SCML2 is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08958-1-scml2-primary-antibodies-fcm-testing-2.pngAnti-SCML2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-SCML2 antibody (A08958-1). Overlay histogram showing K562 cells stained with A08958-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SCML2 Antibody (A08958-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-smad9-picoband-trade-antibody-a04932-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04932-1-smad9-primary-antibodies-wb-testing-1.jpgAnti-Smad9 Antibody Picoband® Western blot analysis of Smad9 using anti-Smad9 antibody (A04932-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Smad9 antigen affinity purified polyclonal antibody (Catalog # A04932-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Smad9 at approximately 55 kDa. The expected band size for Smad9 is at 49 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-snap25-picoband-trade-antibody-a01625-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01625-1-snap25-primary-antibodies-wb-testing-1.jpgAnti-SNAP25 Antibody Picoband® Western blot analysis of SNAP25 using anti-SNAP25 antibody (A01625-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNAP25 antigen affinity purified polyclonal antibody (Catalog # A01625-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SNAP25 at approximately 24 kDa. The expected band size for SNAP25 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01625-1-snap25-primary-antibodies-fcm-testing-2.pngAnti-SNAP25 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-SNAP25 antibody (A01625-1). Overlay histogram showing SH-SY5Y cells stained with A01625-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SNAP25 Antibody (A01625-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-smc1b-picoband-trade-antibody-a10280-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10280-1-smc1b-primary-antibodies-wb-testing-1.jpgAnti-SMC1B Antibody Picoband® Western blot analysis of SMC1B using anti-SMC1B antibody (A10280-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse testis tissue lysates, Lane 4: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMC1B antigen affinity purified polyclonal antibody (Catalog # A10280-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SMC1B at approximately 150,250 kDa. The expected band size for SMC1B is at 144 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10280-1-smc1b-primary-antibodies-if-testing-2.jpgAnti-SMC1B Antibody Picoband® IF analysis of SMC1B using anti-SMC1B antibody (A10280-1). SMC1B was detected in an immunocytochemical section of U2OA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SMC1B Antibody (A10280-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-smpd3-picoband-trade-antibody-a04641-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04641-smpd3-primary-antibodies-wb-testing-1.jpgAnti-SMPD3 Antibody Picoband® Western blot analysis of SMPD3 using anti-SMPD3 antibody (A04641). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMPD3 antigen affinity purified polyclonal antibody (Catalog # A04641) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SMPD3 at approximately 75 kDa. The expected band size for SMPD3 is at 71 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-smtn-picoband-trade-antibody-a04895-2-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04895-2-smtn-primary-antibodies-wb-testing-1.jpgAnti-SMTN Antibody Picoband® Western blot analysis of SMTN using anti-SMTN antibody (A04895-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Colo320 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat stomach tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse stomach tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SMTN antigen affinity purified polyclonal antibody (Catalog # A04895-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SMTN at approximately 120 kDa. The expected band size for SMTN is at 99 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04895-2-fuca-primary-antibodies-ihc-testing-1.jpgAnti-SMTN Antibody Picoband®IHC analysis of FUCA using anti-FUCA antibody (A04895-2). FUCA was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FUCA Antibody (A04895-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04895-2-fuca-primary-antibodies-ihc-testing-2.jpgAnti-SMTN Antibody Picoband®IHC analysis of FUCA using anti-FUCA antibody (A04895-2). FUCA was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FUCA Antibody (A04895-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04895-2-smtn-primary-antibodies-if-testing-2.jpgAnti-SMTN Antibody Picoband® IF analysis of SMTN using anti-SMTN antibody (A04895-2) and anti-Beta Tubulin antibody (M01857-3). SMTN was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SMTN Antibody (A04895-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-sntb1-picoband-trade-antibody-a09492-3-boster.html2026-03-16T09:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09492-3-stnb1-primary-antibodies-wb-testing-1.jpgAnti-SNTB1 Antibody Picoband® Western blot analysis of SNTB1 using anti-SNTB1 antibody (A09492-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNTB1 antigen affinity purified polyclonal antibody (Catalog # A09492-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SNTB1 at approximately 68 kDa. The expected band size for SNTB1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09492-3-stnb1-primary-antibodies-fcm-testing-2.pngAnti-SNTB1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SNTB1 antibody (A09492-3). Overlay histogram showing JK cells stained with A09492-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SNTB1 Antibody (A09492-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-spag16-picoband-trade-antibody-a09080-3-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09080-3-spag16-primary-antibodies-wb-testing-1.jpgAnti-SPAG16 Antibody Picoband® Western blot analysis of SPAG16 using anti-SPAG16 antibody (A09080-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPAG16 antigen affinity purified polyclonal antibody (Catalog # A09080-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SPAG16 at approximately 71 kDa. The expected band size for SPAG16 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09080-3-spag16-primary-antibodies-fcm-testing-2.pngAnti-SPAG16 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-SPAG16 antibody (A09080-3). Overlay histogram showing SH-SY5Y cells stained with A09080-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SPAG16 Antibody (A09080-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-spa17-picoband-trade-antibody-a07969-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-wb-testing-1.jpgAnti-SPA17 Antibody Picoband® Western blot analysis of SPA17 using anti-SPA17 antibody (A07969). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPA17 antigen affinity purified polyclonal antibody (Catalog # A07969) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SPA17 at approximately 22 kDa. The expected band size for SPA17 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-2.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-3.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-4.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-5.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-6.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-7.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-8.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-ihc-testing-9.jpgAnti-SPA17 Antibody Picoband® IHC analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-if-testing-10.jpgAnti-SPA17 Antibody Picoband® IF analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. FITC Conjugated Goat Anti-Rabbit IgG (BA1105) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07969-spa17-primary-antibodies-if-testing-11.jpgAnti-SPA17 Antibody Picoband® IF analysis of SPA17 using anti-SPA17 antibody (A07969). SPA17 was detected in a paraffin-embedded section of human ovarian tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SPA17 Antibody (A07969) overnight at 4°C. FITC Conjugated Goat Anti-Rabbit IgG (BA1105) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-pdx1-picoband-trade-antibody-a00491-4-boster.html2026-03-16T09:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00491-4-pdx1-primary-antibodies-wb-testing-1.jpgAnti-PDX1 Antibody Picoband® Western blot analysis of PDX1 using anti-PDX1 antibody (A00491-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDX1 antigen affinity purified polyclonal antibody (Catalog # A00491-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDX1 at approximately 40 kDa. The expected band size for PDX1 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00491-4-pdx1-primary-antibodies-if-testing-2.jpgAnti-PDX1 Antibody Picoband® IF analysis of PDX1 using anti-PDX1 antibody (A00491-4) and anti-Beta Tubulin antibody (M01857-3). PDX1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PDX1 Antibody (A00491-4) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00491-4-pdx1-primary-antibodies-fcm-testing-3.pngAnti-PDX1 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-PDX1 antibody (A00491-4). Overlay histogram showing Caco-2 cells stained with A00491-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDX1 Antibody (A00491-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ddx58-rig-1-picoband-trade-antibody-a00244-3-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-wb-testing-1.jpgAnti-DDX58/RIG-1 Antibody Picoband® Western blot analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DDX58/RIG-1 antigen affinity purified polyclonal antibody (Catalog # A00244-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DDX58/RIG-1 at approximately 101 kDa. The expected band size for DDX58/RIG-1 is at 107 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-2.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human appendicitis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-3.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human appendicitis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-4.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-5.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-6.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-7.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-8.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-9.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-10.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-ihc-testing-11.jpgAnti-DDX58/RIG-1 Antibody Picoband® IHC analysis of DDX58/RIG-1 using anti-DDX58/RIG-1 antibody (A00244-3). DDX58/RIG-1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DDX58/RIG-1 Antibody (A00244-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00244-3-ddx58-primary-antibodies-fcm-testing-12.pngAnti-DDX58/RIG-1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-DDX58/RIG-1 antibody (A00244-3). Overlay histogram showing MCF-7 cells stained with A00244-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DDX58/RIG-1 Antibody (A00244-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-soat1-picoband-trade-antibody-a05096-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-wb-testing-1.jpgAnti-SOAT1 Antibody Picoband® Western blot analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HUH-7 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOAT1 antigen affinity purified polyclonal antibody (Catalog # A05096-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOAT1 at approximately 75 kDa. The expected band size for SOAT1 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-41419_2024_6711_fig1_html.pngAnti-SOAT1 Antibody Picoband®SOAT1 promotes the malignant progression of HCC. A Up-regulated and down-regulated differentially expression genes (DEGs) in five mRNA expression profiles. B The GO category for DEGs. BP biological process, CC cellular component, MF molecular function. The color represents the P value, and the size indicates the enrichment gene number of each pathway. C KEGG enrichment pathways of DEGs. EIP Environmental Information Processing, CP Cellular Processes, OS Organismal Systems, GIP Genetic Information Processing, HD Human Diseases, M Metabolism. D Protein–protein interaction network of DEGs. E Up-regulated gene expression of lipid metabolism and tumor progression. F Representative images of IHC staining for SOAT1 of normal liver and HCC tissues cited from The Human Protein Atlas. G SOAT1 expression level in normal tissues and HCC tissues based on the TCGA dataset. H , I Analysis of the SOAT1 expression levels in TCGA HCC samples based on the individual clinical stage ( H ) and pathological grade ( I ). J High SOAT1 expression is positively correlated with poor survival ( P = 0.0175). K Representative images of positive and negative SOAT1 expression in different HCC tissues detected by IHC. L Analysis of the expression levels of SOAT1 in HCC patient liver tissues based on ES grade and MVI grade. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-024-06711-9'>38724499</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-41419_2024_6711_fig2_html.pngAnti-SOAT1 Antibody Picoband®SOAT1 promotes the EMT in HCC cells. A SOAT1 expression level in different HCC cell lines cited from CCLE database. B Western blot analysis of SOAT1 expression in HepG2 and PLC/PRF/5 cell lines. C Western blot analysis of EMT related markers in SOAT1 overexpressed or knocked down cells. D Immunofluorescence assay of E-cadherin and Vimentin in cells treated with SOAT1 overexpression or shRNA vectors. E Cell phenotype changes under SOAT1 overexpressed or knocked down treatment. F , G Migration ( F ) and invasion ( G ) of HepG2 cells transfected with SOAT1 or PLC/PRF/5 cells transfected with shSOAT1. H Cell proliferation under SOAT1 overexpressed or knocked down treatment. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-024-06711-9'>38724499</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-41419_2024_6711_fig3_html.pngAnti-SOAT1 Antibody Picoband®SOAT1 induces the EMT via regulating cholesterol metabolism. A , B Oil red O ( A ) and BODIPY 493/503 ( B ) staining of lipid droplets in SOAT1 overexpressed HepG2 cells and SOAT1 knocked down PLC/PRF/5 cells. The relative Oil red O and intensity of BODIPY493/503 were analyzed. C SOAT1 increased accumulation of cholesterol esters. D Cellular cholesterol distribution by Filipin III staining. E Western blot analysis of SOAT1, SREBP2, LDLR, ITGAV, and ITGB4 expression levels under SOAT1 overexpression or knockdown. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-024-06711-9'>38724499</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-41419_2024_6711_fig4_html.pngAnti-SOAT1 Antibody Picoband®Nootkatone alleviates cholesterol metabolism disorder by targeting SOAT1. A Prediction docking score between small-molecule compounds and SOAT1. B Predicted interaction of nootkatone with cavity residues of SOAT1. C Cell viability of HCC cells with nootkatone treatment for 48 h. D , E Micrographs of Oil red O ( D ) and BODIPY ( E ) staining of lipid droplets in PLC/PRF/5 induced with cholesterol (200 μg/mL) for 24 h and then treated with nootkatone (150 and 300 µM) for 48 h. F Nootkatone decreased the content of cholesterol esters in different groups. G , H Expression of SOAT1 in different groups. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-024-06711-9'>38724499</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-41419_2024_6711_fig5_html.pngAnti-SOAT1 Antibody Picoband®Nootkatone inhibits EMT of HCC by targeting SOAT1. A BODIPY493/503 staining of lipid droplets in Control, NK, SOAT1 and SOAT1 + NK groups. B Content of cholesterol esters in different groups. C Cholesterol distribution was determined by Filipin III staining. D , E Invasion ( D ) and migration ( E ) of PLC/PRF/5 cells with different treatments. F Immunofluorescence assay of E-cadherin and Vimentin of cells in different group. G Cell phenotype under nootkatone treatment with different concentration (150 and 300 µM). H Western blot analysis of SOAT1, SREBP2, LDLR, E-cadherin, Occludin, Vimentin, Twist1, N-cadherin, Snail1, Slug, and Fibronectin expression level in different groups. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-024-06711-9'>38724499</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-41419_2024_6711_fig6_html.pngAnti-SOAT1 Antibody Picoband®Nootkatone suppresses the oncogenic and metastatic effects of SOAT1 in vivo. A Representative images of subcutaneous tumor xenografts in Control, SOAT1, shSOAT1, NK and SOAT1 + NK groups. B Tumor volume in different groups. C WB analysis of SOAT1, SREBP2, LDLR, E-cadherin, Occludin, Vimentin, Twist1, N-cadherin, Snail1, Slug, and Fibronectin expression levels in tumor tissue of different groups. D Visible metastatic nodules on the surface of lungs in different groups. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-024-06711-9'>38724499</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-41419_2024_6711_fig7_html.pngAnti-SOAT1 Antibody Picoband®Nootkatone suppresses tumorigenesis and development of NAFLD-HCC mice. A Schematic illustration of experimental procedure. B Representative macroscopic images of liver in Control, Model, NK-L, and NK-H groups. C AFP expression in serum and liver tissue of mice in different groups. D Body weight of mice in different groups. E , F Liver weight ( E ) and liver weight-to-body weight ratio ( F ). G Serum TC level in four groups. H Contents of hepatic free cholesterol and cholesterol esters in four different groups. I Serum ALT and AST level in different groups. J Morphological observations of the liver and liver tissue with Oil red O, H&E and Sirius red staining. The relative Oil red O and Sirius red were obtained through the Image J Pro software. K The protein expression level of SOAT1, SREBP2, LDLR, E-cadherin, Occludin, Vimentin, Twist1, N-cadherin, Snail1, Slug, and Fibronectin expression in liver tissue of mice in different groups. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41419-024-06711-9'>38724499</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-2.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-3.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-4.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-5.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-6.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-7.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-8.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-ihc-testing-9.jpgAnti-SOAT1 Antibody Picoband® IHC analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-if-testing-10.jpgAnti-SOAT1 Antibody Picoband® IF analysis of SOAT1 using anti-SOAT1 antibody (A05096-1). SOAT1 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SOAT1 Antibody (A05096-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-fcm-testing-11.pngAnti-SOAT1 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-SOAT1 antibody (A05096-1). Overlay histogram showing Caco-2 cells stained with A05096-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SOAT1 Antibody (A05096-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05096-1-soat1-primary-antibodies-fcm-testing-12.pngAnti-SOAT1 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-SOAT1 antibody (A05096-1). Overlay histogram showing THP-1 cells stained with A05096-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SOAT1 Antibody (A05096-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-spidr-picoband-trade-antibody-a04260-1-boster.html2026-03-17T05:15:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04260-1-spidr-primary-antibodies-wb-testing-1.jpgAnti-SPIDR Antibody Picoband® Western blot analysis of SPIDR using anti-SPIDR antibody (A04260-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPIDR antigen affinity purified polyclonal antibody (Catalog # A04260-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SPIDR at approximately 95 kDa. The expected band size for SPIDR is at 100 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04260-1-spidr-primary-antibodies-if-testing-2.jpgAnti-SPIDR Antibody Picoband® IF analysis of SPIDR using anti-SPIDR antibody (A04260-1) and anti-Beta Tubulin antibody (M01857-3). SPIDR was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SPIDR Antibody (A04260-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04260-1-spidr-primary-antibodies-fcm-testing-3.pngAnti-SPIDR Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-SPIDR antibody (A04260-1). Overlay histogram showing SiHa cells stained with A04260-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SPIDR Antibody (A04260-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-sssca1-znrd2-picoband-trade-antibody-a14259-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-wb-testing-1.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® Western blot analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat ovary tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SSSCA1/ZNRD2 antigen affinity purified polyclonal antibody (Catalog # A14259-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SSSCA1/ZNRD2 at approximately 23 kDa. The expected band size for SSSCA1/ZNRD2 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-2.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-3.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-4.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-5.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human lung squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-6.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-7.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-8.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-ihc-testing-9.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IHC analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-if-testing-10.jpgAnti-SSSCA1/ZNRD2 Antibody Picoband® IF analysis of SSSCA1/ZNRD2 using anti-SSSCA1/ZNRD2 antibody (A14259-1). SSSCA1/ZNRD2 was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14259-1-sssca1-primary-antibodies-fcm-testing-11.pngAnti-SSSCA1/ZNRD2 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-SSSCA1/ZNRD2 antibody (A14259-1). Overlay histogram showing Hela cells stained with A14259-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SSSCA1/ZNRD2 Antibody (A14259-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stat2-picoband-trade-antibody-a01360-3-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01360-3-stat2-primary-antibodies-wb-testing-1.jpgAnti-STAT2 Antibody Picoband® Western blot analysis of STAT2 using anti-STAT2 antibody (A01360-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HT-1080 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT2 antigen affinity purified polyclonal antibody (Catalog # A01360-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT2 at approximately 113 kDa. The expected band size for STAT2 is at 98 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01360-3-stat2-primary-antibodies-fcm-testing-2.pngAnti-STAT2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-STAT2 antibody (A01360-3). Overlay histogram showing K562 cells stained with A01360-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STAT2 Antibody (A01360-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stk16-picoband-trade-antibody-a10583-1-boster.html2026-03-16T09:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10583-1-stk16-primary-antibodies-wb-testing-1_1.jpgAnti-STK16 Antibody Picoband® Western blot analysis of STK16 using anti-STK16 antibody (A10583-1). Electrophoresis was performed on a10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STK16 antigen affinity purified polyclonal antibody (A10583-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STK16 at approximately 37 kDa. The expected band size for STK16 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10583-1-stk16-primary-antibodies-ihc-testing-1.jpgAnti-STK16 Antibody Picoband®IHC analysis of STK16 using anti-STK16 antibody (A10583-1). STK16 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STK16 Antibody (A10583-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10583-1-stk16-primary-antibodies-ihc-testing-2.jpgAnti-STK16 Antibody Picoband®IHC analysis of STK16 using anti-STK16 antibody (A10583-1). STK16 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STK16 Antibody (A10583-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10583-1-stk16-primary-antibodies-fcm-testing-2.jpgAnti-STK16 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-STK16 antibody (A10583-1). Overlay histogram showing RT4 cells stained with A10583-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STK16 Antibody (A10583-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-stk31-picoband-trade-antibody-a09588-2-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09588-2-stk31-primary-antibodies-wb-testing-1.jpgAnti-STK31 Antibody Picoband® Western blot analysis of STK31 using anti-STK31 antibody (A09588-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STK31 antigen affinity purified polyclonal antibody (Catalog # A09588-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STK31 at approximately 130 kDa. The expected band size for STK31 is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09588-2-stk31-primary-antibodies-ihc-testing-1.jpgAnti-STK31 Antibody Picoband®IHC analysis of STK31 using anti-STK31 antibody (A09588-2). STK31 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STK31 Antibody (A09588-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09588-2-stk31-primary-antibodies-fcm-testing-2.pngAnti-STK31 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-STK31 antibody (A09588-2). Overlay histogram showing MCF-7 cells stained with A09588-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STK31 Antibody (A09588-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09588-2-stk31-primary-antibodies-ihc-testing-2.jpgAnti-STK31 Antibody Picoband®IHC analysis of STK31 using anti-STK31 antibody (A09588-2). STK31 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STK31 Antibody (A09588-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-stk32c-picoband-trade-antibody-a13378-2-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13378-2-stk32c-primary-antibodies-wb-testing-1.jpgAnti-STK32C Antibody Picoband® Western blot analysis of STK32C using anti-STK32C antibody (A13378-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STK32C antigen affinity purified polyclonal antibody (Catalog # A13378-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STK32C at approximately 60,43 kDa. The expected band size for STK32C is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13378-2-stk32c-primary-antibodies-fcm-testing-2.pngAnti-STK32C Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-STK32C antibody (A13378-2). Overlay histogram showing Hela cells stained with A13378-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STK32C Antibody (A13378-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stoml3-picoband-trade-antibody-a13661-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13661-1-stoml3-primary-antibodies-wb-testing-1.jpgAnti-STOML3 Antibody Picoband® Western blot analysis of STOML3 using anti-STOML3 antibody (A13661-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat ovary tissue lysates, Lane 2: rat SHZ-88 whole cell lysates, Lane 3: mouse ovary tissue lysates, Lane 4: mouse ID8 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STOML3 antigen affinity purified polyclonal antibody (Catalog # A13661-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STOML3 at approximately 36 kDa. The expected band size for STOML3 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13661-1-stoml3-primary-antibodies-ihc-testing-1.jpgAnti-STOML3 Antibody Picoband®IHC analysis of STOML3 using anti-STOML3 antibody (A13661-1). STOML3 was detected in a paraffin-embedded section of human fallopian tube tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STOML3 Antibody (A13661-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13661-1-stoml3-primary-antibodies-if-testing-2.jpgAnti-STOML3 Antibody Picoband® IF analysis of STOML3 using anti-STOML3 antibody (A13661-1). STOML3 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-STOML3 Antibody (A13661-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13661-1-stoml3-primary-antibodies-fcm-testing-3.pngAnti-STOML3 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-STOML3 antibody (A13661-1). Overlay histogram showing MCF-7 cells stained with A13661-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-STOML3 Antibody (A13661-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ssh1-picoband-trade-antibody-a03480-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03480-ssh1-primary-antibodies-wb-testing-1.jpgAnti-SSH1 Antibody Picoband® Western blot analysis of SSH1 using anti-SSH1 antibody (A03480). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human Raji whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SSH1 antigen affinity purified polyclonal antibody (Catalog # A03480) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SSH1 at approximately 150 kDa. The expected band size for SSH1 is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03480-ssh1-primary-antibodies-if-testing-2.jpgAnti-SSH1 Antibody Picoband® IF analysis of SSH1 using anti-SSH1 antibody (A03480). SSH1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SSH1 Antibody (A03480) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03480-ssh1-primary-antibodies-fcm-testing-3.pngAnti-SSH1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-SSH1 antibody (A03480). Overlay histogram showing 293T cells stained with A03480 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SSH1 Antibody (A03480, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ssh3-picoband-trade-antibody-a11609-3-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-3-ssh3-primary-antibodies-wb-testing-1.jpgAnti-SSH3 Antibody Picoband® Western blot analysis of SSH3 using anti-SSH3 antibody (A11609-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293Twhole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SSH3 antigen affinity purified polyclonal antibody (Catalog # A11609-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SSH3 at approximately 95 kDa. The expected band size for SSH3 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-3-ssh3-primary-antibodies-ihc-testing-2.jpgAnti-SSH3 Antibody Picoband® IHC analysis of SSH3 using anti-SSH3 antibody (A11609-3). SSH3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSH3 Antibody (A11609-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-3-ssh3-primary-antibodies-ihc-testing-3.jpgAnti-SSH3 Antibody Picoband® IHC analysis of SSH3 using anti-SSH3 antibody (A11609-3). SSH3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSH3 Antibody (A11609-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-3-ssh3-primary-antibodies-ihc-testing-4.jpgAnti-SSH3 Antibody Picoband® IHC analysis of SSH3 using anti-SSH3 antibody (A11609-3). SSH3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSH3 Antibody (A11609-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-3-ssh3-primary-antibodies-if-testing-5.jpgAnti-SSH3 Antibody Picoband® IF analysis of SSH3 using anti-SSH3 antibody (A11609-3) and anti-Beta Tubulin antibody (M01857-3). SSH3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SSH3 Antibody (A11609-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11609-3-ssh3-primary-antibodies-fcm-testing-6.pngAnti-SSH3 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-SSH3 antibody (A11609-3). Overlay histogram showing RT4 cells stained with A11609-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SSH3 Antibody (A11609-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ssx2ip-picoband-trade-antibody-a05918-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05918-1-ssx2ip-primary-antibodies-wb-testing-1.jpgAnti-SSX2IP Antibody Picoband® Western blot analysis of SSX2IP using anti-SSX2IP antibody (A05918-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SSX2IP antigen affinity purified polyclonal antibody (Catalog # A05918-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SSX2IP at approximately 71 kDa. The expected band size for SSX2IP is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05918-1-ssx2ip-primary-antibodies-ihc-testing-2.jpgAnti-SSX2IP Antibody Picoband® IHC analysis of SSX2IP using anti-SSX2IP antibody (A05918-1). SSX2IP was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSX2IP Antibody (A05918-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05918-1-ssx2ip-primary-antibodies-ihc-testing-3.jpgAnti-SSX2IP Antibody Picoband® IHC analysis of SSX2IP using anti-SSX2IP antibody (A05918-1). SSX2IP was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSX2IP Antibody (A05918-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05918-1-ssx2ip-primary-antibodies-ihc-testing-4.jpgAnti-SSX2IP Antibody Picoband® IHC analysis of SSX2IP using anti-SSX2IP antibody (A05918-1). SSX2IP was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SSX2IP Antibody (A05918-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05918-1-ssx2ip-primary-antibodies-fcm-testing-5.pngAnti-SSX2IP Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-SSX2IP antibody (A05918-1). Overlay histogram showing U251 cells stained with A05918-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SSX2IP Antibody (A05918-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stam2-picoband-trade-antibody-a06533-3-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06533-3-stam2-primary-antibodies-wb-testing-1.jpgAnti-STAM2 Antibody Picoband® Western blot analysis of STAM2 using anti-STAM2 antibody (A06533-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAM2 antigen affinity purified polyclonal antibody (Catalog # A06533-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAM2 at approximately 65-70 kDa. The expected band size for STAM2 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06533-3-stam2-primary-antibodies-if-testing-2.jpgAnti-STAM2 Antibody Picoband® IF analysis of STAM2 using anti-STAM2 antibody (A06533-3) and anti-Beta Tubulin antibody (M01857-3). STAM2 was detected in immunocytochemical section of PC-3 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-STAM2 Antibody (A06533-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06533-3-stam2-primary-antibodies-fcm-testing-3.pngAnti-STAM2 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-STAM2 antibody (A06533-3). Overlay histogram showing Hela cells stained with A06533-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STAM2 Antibody (A06533-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stat5a-b-picoband-trade-antibody-a01087-2-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01087-2-stat5ab-primary-antibodies-wb-testing-1.jpgAnti-STAT5A/B Antibody Picoband® Western blot analysis of STAT5A/B using anti-STAT5A/B antibody (A01087-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STAT5A/B antigen affinity purified polyclonal antibody (Catalog # A01087-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STAT5A/B at approximately 90-95 kDa. The expected band size for STAT5A/B is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01087-2-stat5ab-primary-antibodies-if-testing-2.jpgAnti-STAT5A/B Antibody Picoband® IF analysis of STAT5A/B using anti-STAT5A/B antibody (A01087-2) and anti-Beta Tubulin antibody (M01857-3). STAT5A/B was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-STAT5A/B Antibody (A01087-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01087-2-stat5ab-primary-antibodies-fcm-testing-3.pngAnti-STAT5A/B Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-STAT5A/B antibody (A01087-2). Overlay histogram showing A431 cells stained with A01087-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STAT5A/B Antibody (A01087-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stim2-picoband-trade-antibody-a02345-4-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02345-4-stim2-primary-antibodies-wb-testing-1.jpgAnti-STIM2 Antibody Picoband® Western blot analysis of STIM2 using anti-STIM2 antibody (A02345-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat PC-12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STIM2 antigen affinity purified polyclonal antibody (Catalog # A02345-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STIM2 at approximately 98,100 kDa. The expected band size for STIM2 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02345-4-stim2-primary-antibodies-if-testing-2.jpgAnti-STIM2 Antibody Picoband® IF analysis of STIM2 using anti-STIM2 antibody (A02345-4). STIM2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-STIM2 Antibody (A02345-4) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-strbp-picoband-trade-antibody-a12932-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-wb-testing-1.jpgAnti-STRBP Antibody Picoband® Western blot analysis of STRBP using anti-STRBP antibody (A12932-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STRBP antigen affinity purified polyclonal antibody (Catalog # A12932-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STRBP at approximately 70,80 kDa. The expected band size for STRBP is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-ihc-testing-6.jpgAnti-STRBP Antibody Picoband®IHC analysis of STRBP using anti-STRBP antibody (A12932-1). STRBP was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRBP Antibody (A12932-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-ihc-testing-2.jpgAnti-STRBP Antibody Picoband® IHC analysis of STRBP using anti-STRBP antibody (A12932-1). STRBP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRBP Antibody (A12932-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-ihc-testing-3.jpgAnti-STRBP Antibody Picoband® IHC analysis of STRBP using anti-STRBP antibody (A12932-1). STRBP was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRBP Antibody (A12932-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-ihc-testing-4.jpgAnti-STRBP Antibody Picoband® IHC analysis of STRBP using anti-STRBP antibody (A12932-1). STRBP was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRBP Antibody (A12932-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-ihc-testing-5.jpgAnti-STRBP Antibody Picoband® IHC analysis of STRBP using anti-STRBP antibody (A12932-1). STRBP was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRBP Antibody (A12932-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-if-testing-6.jpgAnti-STRBP Antibody Picoband® IF analysis of STRBP using anti-STRBP antibody (A12932-1). STRBP was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-STRBP Antibody (A12932-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12932-1-strbp-primary-antibodies-fcm-testing-7.pngAnti-STRBP Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-STRBP antibody (A12932-1). Overlay histogram showing MCF-7 cells stained with A12932-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STRBP Antibody (A12932-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-strip1-picoband-trade-antibody-a09470-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09470-1-strip1-primary-antibodies-ihc-testing-4.jpgAnti-STRIP1 Antibody Picoband®IHC analysis of STRIP1 using anti-STRIP1 antibody (A09470-1). STRIP1 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRIP1 Antibody (A09470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09470-1-strip1-primary-antibodies-wb-testing-1_1.jpgAnti-STRIP1 Antibody Picoband®Western blot analysis of STRIP1 using anti-STRIP1 antibody (A09470-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STRIP1 antigen affinity purified polyclonal antibody (A09470-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for STRIP1 at approximately 100 kDa. The expected band size for STRIP1 is at 96 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09470-1-strip1-primary-antibodies-ihc-testing-1.jpgAnti-STRIP1 Antibody Picoband®IHC analysis of STRIP1 using anti-STRIP1 antibody (A09470-1). STRIP1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRIP1 Antibody (A09470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09470-1-strip1-primary-antibodies-ihc-testing-2_1.jpgAnti-STRIP1 Antibody Picoband®IHC analysis of STRIP1 using anti-STRIP1 antibody (A09470-1). STRIP1 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRIP1 Antibody (A09470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09470-1-strip1-primary-antibodies-ihc-testing-3_1.jpgAnti-STRIP1 Antibody Picoband®IHC analysis of STRIP1 using anti-STRIP1 antibody (A09470-1). STRIP1 was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STRIP1 Antibody (A09470-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09470-1-strip1-primary-antibodies-ip-testing-1.jpgAnti-STRIP1 Antibody Picoband®Immunoprecipitating (IP) STRIP1 in RT4 whole cell lysate. Western blot analysis of STRIP1 using anti-STRIP1 antibody (A09470-1); Lane 1: RT4 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-STRIP1 antibody in RT4 whole cell lysate; Lane 3: anti-STRIP1 antibody (2μg) + RT4 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-STRIP1 antigen affinity purified polyclonal antibody (A09470-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for STRIP1 at approximately 100 kDa. The expected band size for STRIP1 is at 96 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09470-1-strip1-primary-antibodies-fcm-testing-1.jpgAnti-STRIP1 Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-STRIP1 antibody (A09470-1). Overlay histogram showing SH-SY5Y cells stained with A09470-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STRIP1 Antibody (A09470-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-syntaxin-12-stx12-picoband-trade-antibody-a09232-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09232-1-stx12-primary-antibodies-wb-testing-1.jpgAnti-Syntaxin 12/STX12 Antibody Picoband® Western blot analysis of Syntaxin 12/STX12 using anti-Syntaxin 12/STX12 antibody (A09232-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human LNCAP whole cell lysates, Lane 2: human MDA-MB-453 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Syntaxin 12/STX12 antigen affinity purified polyclonal antibody (Catalog # A09232-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Syntaxin 12/STX12 at approximately 37 kDa. The expected band size for Syntaxin 12/STX12 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09232-1-stx12-primary-antibodies-ihc-testing-1.jpgAnti-Syntaxin 12/STX12 Antibody Picoband®IHC analysis of Syntaxin 12/STX12 using anti-Syntaxin 12/STX12 antibody (A09232-1). Syntaxin 12/STX12 was detected in a paraffin-embedded section of human cerebral cortex tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Syntaxin 12/STX12 Antibody (A09232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09232-1-stx12-primary-antibodies-if-testing-2.jpgAnti-Syntaxin 12/STX12 Antibody Picoband® IF analysis of Syntaxin 12/STX12 using anti-Syntaxin 12/STX12 antibody (A09232-1) and anti-Beta Tubulin antibody (M01857-3). Syntaxin 12/STX12 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Syntaxin 12/STX12 Antibody (A09232-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09232-1-stx12-primary-antibodies-fcm-testing-3.pngAnti-Syntaxin 12/STX12 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-Syntaxin 12/STX12 antibody (A09232-1). Overlay histogram showing 293T cells stained with A09232-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Syntaxin 12/STX12 Antibody (A09232-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-stxbp6-picoband-trade-antibody-a11292-2-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11292-2-stxbp6-primary-antibodies-wb-testing-1.jpgAnti-STXBP6 Antibody Picoband® Western blot analysis of STXBP6 using anti-STXBP6 antibody (A11292-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human Ramos whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STXBP6 antigen affinity purified polyclonal antibody (Catalog # A11292-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STXBP6 at approximately 26 kDa. The expected band size for STXBP6 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11292-2-stxbp6-primary-antibodies-ihc-testing-2.jpgAnti-STXBP6 Antibody Picoband® IHC analysis of STXBP6 using anti-STXBP6 antibody (A11292-2). STXBP6 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STXBP6 Antibody (A11292-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11292-2-stxbp6-primary-antibodies-ihc-testing-3.jpgAnti-STXBP6 Antibody Picoband® IHC analysis of STXBP6 using anti-STXBP6 antibody (A11292-2). STXBP6 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STXBP6 Antibody (A11292-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11292-2-stxbp6-primary-antibodies-ihc-testing-4.jpgAnti-STXBP6 Antibody Picoband® IHC analysis of STXBP6 using anti-STXBP6 antibody (A11292-2). STXBP6 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STXBP6 Antibody (A11292-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11292-2-stxbp6-primary-antibodies-ihc-testing-5.jpgAnti-STXBP6 Antibody Picoband® IHC analysis of STXBP6 using anti-STXBP6 antibody (A11292-2). STXBP6 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-STXBP6 Antibody (A11292-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11292-2-stxbp6-primary-antibodies-fcm-testing-6.pngAnti-STXBP6 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-STXBP6 antibody (A11292-2). Overlay histogram showing HEL cells stained with A11292-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-STXBP6 Antibody (A11292-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-surf6-picoband-trade-antibody-a11571-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11571-1-surf6-primary-antibodies-wb-testing-1.jpgAnti-SURF6 Antibody Picoband® Western blot analysis of SURF6 using anti-SURF6 antibody (A11571-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SURF6 antigen affinity purified polyclonal antibody (Catalog # A11571-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SURF6 at approximately 45 kDa. The expected band size for SURF6 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11571-1-surf6-primary-antibodies-if-testing-2.jpgAnti-SURF6 Antibody Picoband® IF analysis of SURF6 using anti-SURF6 antibody (A11571-1) and anti-Beta Tubulin antibody (M01857-3). SURF6 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SURF6 Antibody (A11571-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-sycn-picoband-trade-antibody-a17780-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17780-1-sycn-primary-antibodies-wb-testing-1.jpgAnti-SYCN Antibody Picoband® Western blot analysis of SYCN using anti-SYCN antibody (A17780-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat pancreas tissue lysates, Lane 2: mouse pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SYCN antigen affinity purified polyclonal antibody (Catalog # A17780-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SYCN at approximately 14 kDa. The expected band size for SYCN is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17780-1-sycn-primary-antibodies-if-testing-2.jpgAnti-SYCN Antibody Picoband® IF analysis of SYCN using anti-SYCN antibody (A17780-1). SYCN was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SYCN Antibody (A17780-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17780-1-sycn-primary-antibodies-fcm-testing-3.pngAnti-SYCN Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-SYCN antibody (A17780-1). Overlay histogram showing K562 cells stained with A17780-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SYCN Antibody (A17780-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-synaptogyrin-1-picoband-trade-antibody-a10148-1-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10148-1-syngr1-primary-antibodies-wb-testing-1.jpgAnti-Synaptogyrin 1 Antibody Picoband® Western blot analysis of Synaptogyrin 1 using anti-Synaptogyrin 1 antibody (A10148-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Synaptogyrin 1 antigen affinity purified polyclonal antibody (Catalog # A10148-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Synaptogyrin 1 at approximately 28 kDa. The expected band size for Synaptogyrin 1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10148-1-syngr1-primary-antibodies-ihc-testing-1.jpgAnti-Synaptogyrin 1 Antibody Picoband®IHC analysis of SYNGR1 using anti-SYNGR1 antibody (A10148-1). SYNGR1 was detected in a paraffin-embedded section of human cerebral cortex tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SYNGR1 Antibody (A10148-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10148-1-syngr1-primary-antibodies-if-testing-2.jpgAnti-Synaptogyrin 1 Antibody Picoband® IF analysis of Synaptogyrin 1 using anti-Synaptogyrin 1 antibody (A10148-1). Synaptogyrin 1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Synaptogyrin 1 Antibody (A10148-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10148-1-syngr1-primary-antibodies-fcm-testing-3.pngAnti-Synaptogyrin 1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-Synaptogyrin 1 antibody (A10148-1). Overlay histogram showing RT4 cells stained with A10148-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Synaptogyrin 1 Antibody (A10148-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rab1a-picoband-trade-antibody-a02682-2-boster.html2026-03-17T05:15:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02682-2-rab1-primary-antibodies-wb-testing-1.jpgAnti-RAB1A Antibody Picoband® Western blot analysis of RAB1A using anti-RAB1A antibody (A02682-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB1A antigen affinity purified polyclonal antibody (Catalog # A02682-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAB1A at approximately 23,22 kDa. The expected band size for RAB1A is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02682-2-rab1-primary-antibodies-fcm-testing-2.pngAnti-RAB1A Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-RAB1A antibody (A02682-2). Overlay histogram showing A549 cells stained with A02682-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAB1A Antibody (A02682-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-syncoilin-sync-picoband-trade-antibody-a06159-1-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06159-1-sync-primary-antibodies-wb-testing-1.jpgAnti-Syncoilin/SYNC Antibody Picoband® Western blot analysis of Syncoilin/SYNC using anti-Syncoilin/SYNC antibody (A06159-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Syncoilin/SYNC antigen affinity purified polyclonal antibody (Catalog # A06159-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Syncoilin/SYNC at approximately 55 kDa. The expected band size for Syncoilin/SYNC is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06159-1-sync-primary-antibodies-if-testing-2.jpgAnti-Syncoilin/SYNC Antibody Picoband® IF analysis of Syncoilin/SYNC using anti-Syncoilin/SYNC antibody (A06159-1). Syncoilin/SYNC was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Syncoilin/SYNC Antibody (A06159-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-syncoilin-sync-picoband-trade-antibody-a06159-2-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06159-2-sync-primary-antibodies-wb-testing-1.jpgAnti-Syncoilin/Sync Antibody Picoband® Western blot analysis of Syncoilin/Sync using anti-Syncoilin/Sync antibody (A06159-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skeletal muscle tissue lysates, Lane 2: rat heart tissue lysates, Lane 3: rat H9C2(2-1) whole cell lysates, Lane 4: rat L6 whole cell lysates, Lane 5: mouse heart tissue lysates, Lane 6: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Syncoilin/Sync antigen affinity purified polyclonal antibody (Catalog # A06159-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Syncoilin/Sync at approximately 72 kDa. The expected band size for Syncoilin/Sync is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06159-2-sync-primary-antibodies-fcm-testing-2.pngAnti-Syncoilin/Sync Antibody Picoband® Flow Cytometry analysis of C2C12 cells using anti-Syncoilin/Sync antibody (A06159-2). Overlay histogram showing C2C12 cells stained with A06159-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Syncoilin/Sync Antibody (A06159-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-synj2-picoband-trade-antibody-a08206-1-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08206-1-synj2-primary-antibodies-wb-testing-1.jpgAnti-SYNJ2 Antibody Picoband® Western blot analysis of SYNJ2 using anti-SYNJ2 antibody (A08206-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SYNJ2 antigen affinity purified polyclonal antibody (Catalog # A08206-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SYNJ2 at approximately 200 kDa. The expected band size for SYNJ2 is at 166 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08206-1-synj2-primary-antibodies-ihc-testing-1.jpgAnti-SYNJ2 Antibody Picoband®IHC analysis of SYNJ2 using anti-SYNJ2 antibody (A08206-1). SYNJ2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SYNJ2 Antibody (A08206-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08206-1-synj2-primary-antibodies-fcm-testing-2.pngAnti-SYNJ2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SYNJ2 antibody (A08206-1). Overlay histogram showing JK cells stained with A08206-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SYNJ2 Antibody (A08206-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08206-1-synj2-primary-antibodies-ihc-testing-2.jpgAnti-SYNJ2 Antibody Picoband®IHC analysis of SYNJ2 using anti-SYNJ2 antibody (A08206-1). SYNJ2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SYNJ2 Antibody (A08206-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-synm-picoband-trade-antibody-a06653-1-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06653-1-synm-primary-antibodies-wb-testing-1.jpgAnti-SYNM Antibody Picoband® Western blot analysis of SYNM using anti-SYNM antibody (A06653-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SYNM antigen affinity purified polyclonal antibody (Catalog # A06653-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SYNM at approximately 180 kDa. The expected band size for SYNM is at 173 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06653-1-synm-primary-antibodies-fcm-testing-2.pngAnti-SYNM Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-SYNM antibody (A06653-1). Overlay histogram showing THP-1 cells stained with A06653-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SYNM Antibody (A06653-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-synpo2-picoband-trade-antibody-a07616-1-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07616-1-synpo2-primary-antibodies-wb-testing-1.jpgAnti-SYNPO2 Antibody Picoband® Western blot analysis of SYNPO2 using anti-SYNPO2 antibody (A07616-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SYNPO2 antigen affinity purified polyclonal antibody (Catalog # A07616-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SYNPO2 at approximately 160 kDa. The expected band size for SYNPO2 is at 118 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07616-1-synpo2-primary-antibodies-fcm-testing-2.pngAnti-SYNPO2 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-SYNPO2 antibody (A07616-1). Overlay histogram showing SH-SY5Y cells stained with A07616-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SYNPO2 Antibody (A07616-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-atp1a4-picoband-trade-antibody-a09005-boster.html2026-03-16T09:42:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09005-atp1a4-primary-antibodies-wb-testing-1.jpgAnti-ATP1A4 Antibody Picoband® Western blot analysis of ATP1A4 using anti-ATP1A4 antibody (A09005). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat C6 whole cell lysates, Lane 2: mouse testis tissue lysates, Lane 3: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP1A4 antigen affinity purified polyclonal antibody (Catalog # A09005) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP1A4 at approximately 100 kDa. The expected band size for ATP1A4 is at 114 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09005-atp1a4-primary-antibodies-fcm-testing-2.pngAnti-ATP1A4 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-ATP1A4 antibody (A09005). Overlay histogram showing MCF-7 cells stained with A09005 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ATP1A4 Antibody (A09005, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-bccip-picoband-trade-antibody-a05912-2-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-wb-testing-1.jpgAnti-BCCIP Antibody Picoband® Western blot analysis of BCCIP using anti-BCCIP antibody (A05912-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCCIP antigen affinity purified polyclonal antibody (Catalog # A05912-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCCIP at approximately 45 kDa. The expected band size for BCCIP is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-ihc-testing-8.jpgAnti-BCCIP Antibody Picoband®IHC analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in a paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-ihc-testing-2.jpgAnti-BCCIP Antibody Picoband® IHC analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-ihc-testing-3.jpgAnti-BCCIP Antibody Picoband® IHC analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-ihc-testing-4.jpgAnti-BCCIP Antibody Picoband® IHC analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-ihc-testing-5.jpgAnti-BCCIP Antibody Picoband® IHC analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-ihc-testing-6.jpgAnti-BCCIP Antibody Picoband® IHC analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-ihc-testing-7.jpgAnti-BCCIP Antibody Picoband® IHC analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-if-testing-8.jpgAnti-BCCIP Antibody Picoband® IF analysis of BCCIP using anti-BCCIP antibody (A05912-2). BCCIP was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BCCIP Antibody (A05912-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05912-2-bccip-primary-antibodies-fcm-testing-9.pngAnti-BCCIP Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-BCCIP antibody (A05912-2). Overlay histogram showing Caco-2 cells stained with A05912-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BCCIP Antibody (A05912-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-bim-bcl2l11-picoband-trade-antibody-a01552-5-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01552-5-bcl2l11-primary-antibodies-wb-testing-1.jpgAnti-Bim/Bcl2l11 Antibody Picoband® Western blot analysis of Bim/Bcl2l11 using anti-Bim/Bcl2l11 antibody (A01552-5). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse spleen tissue lysates, Lane 2: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Bim/Bcl2l11 antigen affinity purified polyclonal antibody (Catalog # A01552-5) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Bim/Bcl2l11 at approximately 22 kDa. The expected band size for Bim/Bcl2l11 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01552-5-bcl2l11-primary-antibodies-fcm-testing-2.pngAnti-Bim/Bcl2l11 Antibody Picoband® Flow Cytometry analysis of C2C12 cells using anti-Bim/Bcl2l11 antibody (A01552-5). Overlay histogram showing C2C12 cells stained with A01552-5 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Bim/Bcl2l11 Antibody (A01552-5, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-cd300a-picoband-trade-antibody-a05953-1-boster.html2026-03-16T09:42:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05953-1-cd300a-primary-antibodies-wb-testing-1.jpgAnti-CD300A Antibody Picoband® Western blot analysis of CD300A using anti-CD300A antibody (A05953-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HL-60 whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse Raw264.7 whole cell lysates, Lane 6: mouse J774A.1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD300A antigen affinity purified polyclonal antibody (Catalog # A05953-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD300A at approximately 68 kDa. The expected band size for CD300A is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05953-1-cd300a-primary-antibodies-fcm-testing-2.pngAnti-CD300A Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-CD300A antibody (A05953-1). Overlay histogram showing U20S cells stained with A05953-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD300A Antibody (A05953-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-cdca8-picoband-trade-antibody-a06612-2-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06612-2-cdca8-primary-antibodies-wb-testing-1.jpgAnti-CDCA8 Antibody Picoband® Western blot analysis of CDCA8 using anti-CDCA8 antibody (A06612-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDCA8 antigen affinity purified polyclonal antibody (Catalog # A06612-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDCA8 at approximately 35 kDa. The expected band size for CDCA8 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06612-2-cdca8-primary-antibodies-if-testing-2.jpgAnti-CDCA8 Antibody Picoband® IF analysis of CDCA8 using anti-CDCA8 antibody (A06612-2) and anti-Beta Tubulin antibody (M01857-3). CDCA8 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CDCA8 Antibody (A06612-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06612-2-cdca8-primary-antibodies-fcm-testing-3.pngAnti-CDCA8 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-CDCA8 antibody (A06612-2). Overlay histogram showing K562 cells stained with A06612-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CDCA8 Antibody (A06612-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-cep63-picoband-trade-antibody-a01661-1-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01661-1-cep63-primary-antibodies-wb-testing-1.jpgAnti-CEP63 Antibody Picoband® Western blot analysis of CEP63 using anti-CEP63 antibody (A01661-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CEP63 antigen affinity purified polyclonal antibody (Catalog # A01661-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CEP63 at approximately 70 kDa. The expected band size for CEP63 is at 81 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-lat-picoband-trade-antibody-a01654-1-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-1-lat-primary-antibodies-wb-testing-1.jpgAnti-LAT Antibody Picoband® Western blot analysis of LAT using anti-LAT antibody (A01654-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LAT antigen affinity purified polyclonal antibody (Catalog # A01654-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LAT at approximately 37 kDa. The expected band size for LAT is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-1-lat-primary-antibodies-fcm-testing-2.pngAnti-LAT Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-LAT antibody (A01654-1). Overlay histogram showing HEL cells stained with A01654-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LAT Antibody (A01654-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-lat-picoband-trade-antibody-a01654-2-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-wb-testing-1.jpgAnti-Lat Antibody Picoband® Western blot analysis of Lat using anti-Lat antibody (A01654-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lat antigen affinity purified polyclonal antibody (Catalog # A01654-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lat at approximately 38 kDa. The expected band size for Lat is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-2.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of mouse intestinal lymph nodes tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-3.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-4.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-5.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of mouse intestinal lymph nodes tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-6.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of rat intestinal lymph nodes tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-7.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of rat lymph node tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-8.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-ihc-testing-9.jpgAnti-Lat Antibody Picoband® IHC analysis of Lat using anti-Lat antibody (A01654-2). Lat was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lat Antibody (A01654-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01654-2-lat-primary-antibodies-fcm-testing-10.pngAnti-Lat Antibody Picoband® Flow Cytometry analysis of Raw264.7 cells using anti-Lat antibody (A01654-2). Overlay histogram showing Raw264.7 cells stained with A01654-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Lat Antibody (A01654-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nup62-picoband-trade-antibody-a03950-2-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03950-2-nup62-primary-antibodies-wb-testing-1.jpgAnti-NUP62 Antibody Picoband® Western blot analysis of NUP62 using anti-NUP62 antibody (A03950-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse testis tissue lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP62 antigen affinity purified polyclonal antibody (Catalog # A03950-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP62 at approximately 69 kDa. The expected band size for NUP62 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03950-2-nup62-primary-antibodies-ihc-testing-2.jpgAnti-NUP62 Antibody Picoband® IHC analysis of NUP62 using anti-NUP62 antibody (A03950-2). NUP62 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP62 Antibody (A03950-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03950-2-nup62-primary-antibodies-if-testing-3.jpgAnti-NUP62 Antibody Picoband® IF analysis of NUP62 using anti-NUP62 antibody (A03950-2) and anti-Beta Tubulin antibody (M01857-3). NUP62 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP62 Antibody (A03950-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03950-2-nup62-primary-antibodies-if-testing-4.jpgAnti-NUP62 Antibody Picoband® IF analysis of NUP62 using anti-NUP62 antibody (A03950-2). NUP62 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP62 Antibody (A03950-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03950-2-nup62-primary-antibodies-fcm-testing-5.pngAnti-NUP62 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-NUP62 antibody (A03950-2). Overlay histogram showing PC-3 cells stained with A03950-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUP62 Antibody (A03950-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rad51d-picoband-trade-antibody-a02893-3-boster.html2026-03-17T05:15:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02893-3-rad51d-primary-antibodies-wb-testing-1.jpgAnti-RAD51D Antibody Picoband® Western blot analysis of RAD51D using anti-RAD51D antibody (A02893-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human A2780 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAD51D antigen affinity purified polyclonal antibody (Catalog # A02893-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAD51D at approximately 30-40 kDa. The expected band size for RAD51D is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02893-3-rad51d-primary-antibodies-ihc-testing-1.jpgAnti-RAD51D Antibody Picoband®IHC analysis of RAD51D using anti-RAD51D antibody (A02893-3). RAD51D was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAD51D Antibody (A02893-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02893-3-rad51d-primary-antibodies-if-testing-2.jpgAnti-RAD51D Antibody Picoband® IF analysis of RAD51D using anti-RAD51D antibody (A02893-3) and anti-Beta Tubulin antibody (M01857-3). RAD51D was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RAD51D Antibody (A02893-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02893-3-rad51d-primary-antibodies-fcm-testing-3.pngAnti-RAD51D Antibody Picoband® Flow Cytometry analysis of JK cells using anti-RAD51D antibody (A02893-3). Overlay histogram showing JK cells stained with A02893-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAD51D Antibody (A02893-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rfxank-picoband-trade-antibody-a07934-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07934-rfxank-primary-antibodies-wb-testing-1.jpgAnti-RFXANK Antibody Picoband® Western blot analysis of RFXANK using anti-RFXANK antibody (A07934). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RFXANK antigen affinity purified polyclonal antibody (Catalog # A07934) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RFXANK at approximately 34 kDa. The expected band size for RFXANK is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07934-rfxank-primary-antibodies-if-testing-2.jpgAnti-RFXANK Antibody Picoband® IF analysis of RFXANK using anti-RFXANK antibody (A07934) and anti-Beta Tubulin antibody (M01857-3). RFXANK was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RFXANK Antibody (A07934) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07934-rfxank-primary-antibodies-fcm-testing-3.pngAnti-RFXANK Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-RFXANK antibody (A07934). Overlay histogram showing PC-3 cells stained with A07934 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RFXANK Antibody (A07934, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rilpl1-picoband-trade-antibody-a13355-1-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13355-1-rilpl1-primary-antibodies-wb-testing-1.jpgAnti-RILPL1 Antibody Picoband® Western blot analysis of RILPL1 using anti-RILPL1 antibody (A13355-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human H9C2(2-1) whole cell lysates, Lane 2: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RILPL1 antigen affinity purified polyclonal antibody (Catalog # A13355-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RILPL1 at approximately 50 kDa. The expected band size for RILPL1 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13355-1-rilpl1-primary-antibodies-fcm-testing-2.pngAnti-RILPL1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-RILPL1 antibody (A13355-1). Overlay histogram showing 293T cells stained with A13355-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RILPL1 Antibody (A13355-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rad54l2-picoband-trade-antibody-a11741-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11741-rad54l2-primary-antibodies-wb-testing-1.jpgAnti-RAD54L2 Antibody Picoband® Western blot analysis of RAD54L2 using anti-RAD54L2 antibody (A11741). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse Raw264.7 whole cell lysates, Lane 6: mouse Ana-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAD54L2 antigen affinity purified polyclonal antibody (Catalog # A11741) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAD54L2 at approximately 190 kDa. The expected band size for RAD54L2 is at 163 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11741-rad54l2-primary-antibodies-if-testing-2.jpgAnti-RAD54L2 Antibody Picoband® IF analysis of RAD54L2 using anti-RAD54L2 antibody (A11741) and anti-Beta Tubulin antibody (M01857-3). RAD54L2 was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RAD54L2 Antibody (A11741) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11741-rad54l2-primary-antibodies-fcm-testing-3.pngAnti-RAD54L2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-RAD54L2 antibody (A11741). Overlay histogram showing HEL cells stained with A11741 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAD54L2 Antibody (A11741, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-oxsr1-picoband-trade-antibody-a05141-2-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05141-2-oxsr1-primary-antibodies-wb-testing-1.jpgAnti-OXSR1 Antibody Picoband® Western blot analysis of OXSR1 using anti-OXSR1 antibody (A05141-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OXSR1 antigen affinity purified polyclonal antibody (Catalog # A05141-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OXSR1 at approximately 58 kDa. The expected band size for OXSR1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05141-2-oxsr1-primary-antibodies-fcm-testing-2.pngAnti-OXSR1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-OXSR1 antibody (A05141-2). Overlay histogram showing MCF-7 cells stained with A05141-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-OXSR1 Antibody (A05141-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05141-2-oxsr1-primary-antibodies-ip-testing-3.jpgAnti-OXSR1 Antibody Picoband® Immunoprecipitating OXSR1 in U251 whole cell lysate. Western blot analysis of OXSR1 using anti-OXSR1 antibody (A05141-2). Lane 1: U251 whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-OXSR1 antibody in U251 whole cell lysate. Lane 3: anti-OXSR1 antibody (2μg) + U251 whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-OXSR1 antigen affinity purified polyclonal antibody (A05141-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for OXSR1 at approximately 58 kDa. The expected band size for OXSR1 is at 58 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-pacsin1-picoband-trade-antibody-a06188-2-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-wb-testing-1.jpgAnti-PACSIN1 Antibody Picoband® Western blot analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PACSIN1 antigen affinity purified polyclonal antibody (Catalog # A06188-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PACSIN1 at approximately 51 kDa. The expected band size for PACSIN1 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-ihc-testing-2.jpgAnti-PACSIN1 Antibody Picoband® IHC analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2). PACSIN1 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PACSIN1 Antibody (A06188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-ihc-testing-3.jpgAnti-PACSIN1 Antibody Picoband® IHC analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2). PACSIN1 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PACSIN1 Antibody (A06188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-ihc-testing-4.jpgAnti-PACSIN1 Antibody Picoband® IHC analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2). PACSIN1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PACSIN1 Antibody (A06188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-ihc-testing-5.jpgAnti-PACSIN1 Antibody Picoband® IHC analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2). PACSIN1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PACSIN1 Antibody (A06188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-ihc-testing-6.jpgAnti-PACSIN1 Antibody Picoband® IHC analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2). PACSIN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PACSIN1 Antibody (A06188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-ihc-testing-7.jpgAnti-PACSIN1 Antibody Picoband® IHC analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2). PACSIN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PACSIN1 Antibody (A06188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-if-testing-8.jpgAnti-PACSIN1 Antibody Picoband® IF analysis of PACSIN1 using anti-PACSIN1 antibody (A06188-2) and anti-Beta Tubulin antibody (M01857-3). PACSIN1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PACSIN1 Antibody (A06188-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-fcm-testing-9.pngAnti-PACSIN1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PACSIN1 antibody (A06188-2). Overlay histogram showing JK cells stained with A06188-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PACSIN1 Antibody (A06188-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06188-2-pacsin1-primary-antibodies-fcm-testing-10.pngAnti-PACSIN1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-PACSIN1 antibody (A06188-2). Overlay histogram showing K562 cells stained with A06188-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PACSIN1 Antibody (A06188-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pafah1b2-picoband-trade-antibody-a07067-boster.html2026-03-16T09:42:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07067-pafah1b2-primary-antibodies-wb-testing-1.jpgAnti-PAFAH1B2 Antibody Picoband® Western blot analysis of PAFAH1B2 using anti-PAFAH1B2 antibody (A07067). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAFAH1B2 antigen affinity purified polyclonal antibody (Catalog # A07067) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAFAH1B2 at approximately 26 kDa. The expected band size for PAFAH1B2 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07067-pafah1b2-primary-antibodies-ihc-testing-2.jpgAnti-PAFAH1B2 Antibody Picoband® IHC analysis of PAFAH1B2 using anti-PAFAH1B2 antibody (A07067). PAFAH1B2 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAFAH1B2 Antibody (A07067) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07067-pafah1b2-primary-antibodies-ihc-testing-3.jpgAnti-PAFAH1B2 Antibody Picoband® IHC analysis of PAFAH1B2 using anti-PAFAH1B2 antibody (A07067). PAFAH1B2 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PAFAH1B2 Antibody (A07067) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-pax3-picoband-trade-antibody-a00285-2-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00285-2-pax3-primary-antibodies-wb-testing-1.jpgAnti-PAX3 Antibody Picoband® Western blot analysis of PAX3 using anti-PAX3 antibody (A00285-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A375 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAX3 antigen affinity purified polyclonal antibody (Catalog # A00285-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAX3 at approximately 69 kDa. The expected band size for PAX3 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00285-2-pax3-primary-antibodies-if-testing-2.jpgAnti-PAX3 Antibody Picoband® IF analysis of PAX3 using anti-PAX3 antibody (A00285-2) and anti-Beta Tubulin antibody (M01857-3). PAX3 was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PAX3 Antibody (A00285-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-pbx4-picoband-trade-antibody-a11995-1-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11995-1-pbx4-primary-antibodies-wb-testing-1.jpgAnti-PBX4 Antibody Picoband® Western blot analysis of PBX4 using anti-PBX4 antibody (A11995-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SK-OV-3 whole cell lysates, Lane 3: human A2780 whole cell lysates, Lane 4: human COLO320 whole cell lysates, Lane 5: human Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PBX4 antigen affinity purified polyclonal antibody (Catalog # A11995-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PBX4 at approximately 39 kDa. The expected band size for PBX4 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11995-1-pbx4-primary-antibodies-if-testing-2.jpgAnti-PBX4 Antibody Picoband® IF analysis of PBX4 using anti-PBX4 antibody (A11995-1) and anti-Beta Tubulin antibody (M01857-3). PBX4 was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PBX4 Antibody (A11995-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-osmr-picoband-trade-antibody-a04061-2-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04061-2-osmr-primary-antibodies-wb-testing-1.jpgAnti-Osmr Antibody Picoband® Western blot analysis of Osmr using anti-Osmr antibody (A04061-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat C6 whole cell lysates, Lane 2: rat L6 whole cell lysates, Lane 3: mouse Neuro-2a whole cell lysates, Lane 4: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Osmr antigen affinity purified polyclonal antibody (Catalog # A04061-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Osmr at approximately 110,180 kDa. The expected band size for Osmr is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04061-2-osmr-primary-antibodies-fcm-testing-2.pngAnti-Osmr Antibody Picoband® Flow Cytometry analysis of C2C12 cells using anti-Osmr antibody (A04061-2). Overlay histogram showing C2C12 cells stained with A04061-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Osmr Antibody (A04061-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-otud3-picoband-trade-antibody-a12734-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12734-otud3-primary-antibodies-wb-testing-1.jpgAnti-OTUD3 Antibody Picoband® Western blot analysis of OTUD3 using anti-OTUD3 antibody (A12734). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OTUD3 antigen affinity purified polyclonal antibody (Catalog # A12734) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OTUD3 at approximately 43 kDa. The expected band size for OTUD3 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12734-otud3-primary-antibodies-if-testing-2.jpgAnti-OTUD3 Antibody Picoband® IF analysis of OTUD3 using anti-OTUD3 antibody (A12734). OTUD3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-OTUD3 Antibody (A12734) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-otud5-picoband-trade-antibody-a09744-1-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09744-1-otud5-primary-antibodies-wb-testing-1.jpgAnti-OTUD5 Antibody Picoband® Western blot analysis of OTUD5 using anti-OTUD5 antibody (A09744-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OTUD5 antigen affinity purified polyclonal antibody (Catalog # A09744-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OTUD5 at approximately 75 kDa. The expected band size for OTUD5 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09744-1-otud5-primary-antibodies-if-testing-2.jpgAnti-OTUD5 Antibody Picoband® IF analysis of OTUD5 using anti-OTUD5 antibody (A09744-1) and anti-Beta Tubulin antibody (M01857-3). OTUD5 was detected in immunocytochemical section of A431 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-OTUD5 Antibody (A09744-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-pcyox1-picoband-trade-antibody-a11180-1-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11180-1-pcyox1-primary-antibodies-wb-testing-1.jpgAnti-PCYOX1 Antibody Picoband® Western blot analysis of PCYOX1 using anti-PCYOX1 antibody (A11180-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 5: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCYOX1 antigen affinity purified polyclonal antibody (Catalog # A11180-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCYOX1 at approximately 57 kDa. The expected band size for PCYOX1 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11180-1-pcyox1-primary-antibodies-ihc-testing-2.jpgAnti-PCYOX1 Antibody Picoband® IHC analysis of PCYOX1 using anti-PCYOX1 antibody (A11180-1). PCYOX1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCYOX1 Antibody (A11180-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11180-1-pcyox1-primary-antibodies-ihc-testing-3.jpgAnti-PCYOX1 Antibody Picoband® IHC analysis of PCYOX1 using anti-PCYOX1 antibody (A11180-1). PCYOX1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCYOX1 Antibody (A11180-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11180-1-pcyox1-primary-antibodies-ihc-testing-4.jpgAnti-PCYOX1 Antibody Picoband® IHC analysis of PCYOX1 using anti-PCYOX1 antibody (A11180-1). PCYOX1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCYOX1 Antibody (A11180-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11180-1-pcyox1-primary-antibodies-ihc-testing-5.jpgAnti-PCYOX1 Antibody Picoband® IHC analysis of PCYOX1 using anti-PCYOX1 antibody (A11180-1). PCYOX1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PCYOX1 Antibody (A11180-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11180-1-pcyox1-primary-antibodies-fcm-testing-6.pngAnti-PCYOX1 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-PCYOX1 antibody (A11180-1). Overlay histogram showing SiHa cells stained with A11180-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PCYOX1 Antibody (A11180-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pfkm-picoband-trade-antibody-a00437-2-boster.html2026-03-16T09:42:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-wb-testing-1.jpgAnti-PFKM Antibody Picoband® Western blot analysis of PFKM using anti-PFKM antibody (A00437-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human U-87MG whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PFKM antigen affinity purified polyclonal antibody (Catalog # A00437-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PFKM at approximately 85 kDa. The expected band size for PFKM is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-2.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-3.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-4.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-5.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-6.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-7.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-8.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-9.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-10.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-ihc-testing-11.jpgAnti-PFKM Antibody Picoband® IHC analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-if-testing-12.jpgAnti-PFKM Antibody Picoband® IF analysis of PFKM using anti-PFKM antibody (A00437-2). PFKM was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PFKM Antibody (A00437-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00437-2-pfkm-primary-antibodies-fcm-testing-13.pngAnti-PFKM Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PFKM antibody (A00437-2). Overlay histogram showing 293T cells stained with A00437-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PFKM Antibody (A00437-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mettl17-picoband-trade-antibody-a14339-1-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14339-1-mettl17-primary-antibodies-wb-testing-1.jpgAnti-METTL17 Antibody Picoband® Western blot analysis of METTL17 using anti-METTL17 antibody (A14339-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METTL17 antigen affinity purified polyclonal antibody (Catalog # A14339-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METTL17 at approximately 64 kDa. The expected band size for METTL17 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14339-1-mettl17-primary-antibodies-if-testing-2.jpgAnti-METTL17 Antibody Picoband® IF analysis of METTL17 using anti-METTL17 antibody (A14339-1) and anti-Beta Tubulin antibody (M01857-3). METTL17 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-METTL17 Antibody (A14339-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-mmp12-picoband-trade-antibody-a01520-2-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01520-2-mmp12-primary-antibodies-wb-testing-1.jpgAnti-Mmp12 Antibody Picoband® Western blot analysis of Mmp12 using anti-Mmp12 antibody (A01520-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse thymus tissue lysates, Lane 2: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Mmp12 antigen affinity purified polyclonal antibody (Catalog # A01520-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Mmp12 at approximately 45 kDa. The expected band size for Mmp12 is at 55 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-mmp20-picoband-trade-antibody-a06145-2-boster.html2026-03-17T05:15:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06145-2-mmp20-primary-antibodies-wb-testing-1.jpgAnti-MMP20 Antibody Picoband® Western blot analysis of MMP20 using anti-MMP20 antibody (A06145-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMP20 antigen affinity purified polyclonal antibody (Catalog # A06145-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMP20 at approximately 54 kDa. The expected band size for MMP20 is at 54 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-igsf11-picoband-trade-antibody-a09664-1-boster.html2026-03-16T09:42:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09664-1-igsf11-primary-antibodies-wb-testing-1.jpgAnti-IGSF11 Antibody Picoband® Western blot analysis of IGSF11 using anti-IGSF11 antibody (A09664-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGSF11 antigen affinity purified polyclonal antibody (Catalog # A09664-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGSF11 at approximately 50 kDa. The expected band size for IGSF11 is at 46 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-ifn-gamma-ifng-picoband-trade-antibody-a00393-4-boster.html2026-03-17T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00393-4-ifng-primary-antibodies-wb-testing-1.jpgAnti-IFN Gamma/Ifng Antibody Picoband® Western blot analysis of IFN Gamma/Ifng using anti-IFN Gamma/Ifng antibody (A00393-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. Lane 1: recombinant mouse Ifng protein 5 ng, Lane 1: recombinant mouse Ifng protein 2.5 ng. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFN Gamma/Ifng antigen affinity purified polyclonal antibody (Catalog # A00393-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. https://www.bosterbio.com/products/primary-antibodies/anti-kdm8-picoband-trade-antibody-a08840-2-boster.html2026-03-16T09:42:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08840-2-kdm8-primary-antibodies-wb-testing-1.jpgAnti-KDM8 Antibody Picoband® Western blot analysis of KDM8 using anti-KDM8 antibody (A08840-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-KDM8 antigen affinity purified polyclonal antibody (Catalog # A08840-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for KDM8 at approximately 55 kDa. The expected band size for KDM8 is at 47 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-gja4-picoband-trade-antibody-a05569-1-boster.html2026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05569-1-gja4-primary-antibodies-wb-testing-1_1.jpgAnti-GJA4 Antibody Picoband®Western blot analysis of GJA4 using anti-GJA4 antibody (A05569-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GJA4 antigen affinity purified polyclonal antibody (A05569-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GJA4 at approximately 40 kDa. The expected band size for GJA4 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05569-1-gja4-primary-antibodies-ihc-testing-1.jpgAnti-GJA4 Antibody Picoband®IHC analysis of GJA4 using anti-GJA4 antibody (A05569-1). GJA4 was detected in a paraffin-embedded section of human heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GJA4 Antibody (A05569-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05569-1-gja4-primary-antibodies-ihc-testing-2.jpgAnti-GJA4 Antibody Picoband®IHC analysis of GJA4 using anti-GJA4 antibody (A05569-1). GJA4 was detected in a paraffin-embedded section of human heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GJA4 Antibody (A05569-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-ut-b-slc14a1-picoband-trade-antibody-a04926-2-boster.html2026-03-16T09:42:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-wb-testing-1.jpgAnti-UT-B/SLC14A1 Antibody Picoband® Western blot analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UT-B/SLC14A1 antigen affinity purified polyclonal antibody (Catalog # A04926-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for UT-B/SLC14A1 at approximately 65 kDa. The expected band size for UT-B/SLC14A1 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-2.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-3.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-4.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-5.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of human pancreatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-6.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-7.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-8.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-ihc-testing-9.jpgAnti-UT-B/SLC14A1 Antibody Picoband® IHC analysis of UT-B/SLC14A1 using anti-UT-B/SLC14A1 antibody (A04926-2). UT-B/SLC14A1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-UT-B/SLC14A1 Antibody (A04926-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04926-2-slc14a1-primary-antibodies-fcm-testing-10.pngAnti-UT-B/SLC14A1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-UT-B/SLC14A1 antibody (A04926-2). Overlay histogram showing JK cells stained with A04926-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-UT-B/SLC14A1 Antibody (A04926-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-integrin-alpha-4-itga4-picoband-trade-antibody-a00468-2-boster.html2026-03-17T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00468-2-itga4-primary-antibodies-wb-testing-1.jpgAnti-Integrin Alpha 4/Itga4 Antibody Picoband® Western blot analysis of Integrin Alpha 4/Itga4 using anti-Integrin Alpha 4/Itga4 antibody (A00468-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Integrin Alpha 4/Itga4 antigen affinity purified polyclonal antibody (Catalog # A00468-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Integrin Alpha 4/Itga4 at approximately 150-180 kDa. The expected band size for Integrin Alpha 4/Itga4 is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00468-2-itga4-primary-antibodies-fcm-testing-2.pngAnti-Integrin Alpha 4/Itga4 Antibody Picoband® Flow Cytometry analysis of NIH/3T3 cells using anti-Integrin Alpha 4/Itga4 antibody (A00468-2). Overlay histogram showing NIH/3T3 cells stained with A00468-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Integrin Alpha 4/Itga4 Antibody (A00468-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nptx2-picoband-trade-antibody-a09667-1-boster.html2026-03-17T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09667-1-nptx2-primary-antibodies-wb-testing-1.jpgAnti-NPTX2 Antibody Picoband® Western blot analysis of NPTX2 using anti-NPTX2 antibody (A09667-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NPTX2 antigen affinity purified polyclonal antibody (Catalog # A09667-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NPTX2 at approximately 47 kDa. The expected band size for NPTX2 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09667-1-nptx2-primary-antibodies-ihc-testing-2.jpgAnti-NPTX2 Antibody Picoband® IHC analysis of NPTX2 using anti-NPTX2 antibody (A09667-1). NPTX2 was detected in a paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPTX2 Antibody (A09667-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09667-1-nptx2-primary-antibodies-ihc-testing-3.jpgAnti-NPTX2 Antibody Picoband® IHC analysis of NPTX2 using anti-NPTX2 antibody (A09667-1). NPTX2 was detected in a paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPTX2 Antibody (A09667-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09667-1-nptx2-primary-antibodies-ihc-testing-4.jpgAnti-NPTX2 Antibody Picoband® IHC analysis of NPTX2 using anti-NPTX2 antibody (A09667-1). NPTX2 was detected in a paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPTX2 Antibody (A09667-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09667-1-nptx2-primary-antibodies-ihc-testing-5.jpgAnti-NPTX2 Antibody Picoband® IHC analysis of NPTX2 using anti-NPTX2 antibody (A09667-1). NPTX2 was detected in a paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NPTX2 Antibody (A09667-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-sqrdl-sqor-picoband-trade-antibody-a31817-boster.html2026-03-17T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31817-sqor-primary-antibodies-wb-testing-1.jpgAnti-SQRDL/SQOR Antibody Picoband® Western blot analysis of SQRDL/SQOR using anti-SQRDL/SQOR antibody (A31817). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SQRDL/SQOR antigen affinity purified polyclonal antibody (Catalog # A31817) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SQRDL/SQOR at approximately 50 kDa. The expected band size for SQRDL/SQOR is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31817-sqor-primary-antibodies-ihc-testing-2.jpgAnti-SQRDL/SQOR Antibody Picoband® IHC analysis of SQRDL/SQOR using anti-SQRDL/SQOR antibody (A31817). SQRDL/SQOR was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SQRDL/SQOR Antibody (A31817) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31817-sqor-primary-antibodies-ihc-testing-3.jpgAnti-SQRDL/SQOR Antibody Picoband® IHC analysis of SQRDL/SQOR using anti-SQRDL/SQOR antibody (A31817). SQRDL/SQOR was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SQRDL/SQOR Antibody (A31817) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31817-sqor-primary-antibodies-ihc-testing-4.jpgAnti-SQRDL/SQOR Antibody Picoband® IHC analysis of SQRDL/SQOR using anti-SQRDL/SQOR antibody (A31817). SQRDL/SQOR was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SQRDL/SQOR Antibody (A31817) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31817-sqor-primary-antibodies-ihc-testing-5.jpgAnti-SQRDL/SQOR Antibody Picoband® IHC analysis of SQRDL/SQOR using anti-SQRDL/SQOR antibody (A31817). SQRDL/SQOR was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SQRDL/SQOR Antibody (A31817) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31817-sqor-primary-antibodies-if-testing-6.jpgAnti-SQRDL/SQOR Antibody Picoband® IF analysis of SQRDL/SQOR using anti-SQRDL/SQOR antibody (A31817). SQRDL/SQOR was detected in an immunocytochemical section of PC-3 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SQRDL/SQOR Antibody (A31817) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31817-sqor-primary-antibodies-fcm-testing-7.pngAnti-SQRDL/SQOR Antibody Picoband® Flow Cytometry analysis of JK cells using anti-SQRDL/SQOR antibody (A31817). Overlay histogram showing JK cells stained with A31817 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SQRDL/SQOR Antibody (A31817, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-secisbp2-picoband-trade-antibody-a06543-4-boster.html2026-03-17T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06543-4-secisbp2-primary-antibodies-wb-testing-1.jpgAnti-SECISBP2 Antibody Picoband® Western blot analysis of SECISBP2 using anti-SECISBP2 antibody (A06543-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SECISBP2 antigen affinity purified polyclonal antibody (Catalog # A06543-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SECISBP2 at approximately 105 kDa. The expected band size for SECISBP2 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06543-4-secisbp2-primary-antibodies-if-testing-2.jpgAnti-SECISBP2 Antibody Picoband® IF analysis of SECISBP2 using anti-SECISBP2 antibody (A06543-4) and anti-Beta Tubulin antibody (M01857-3). SECISBP2 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SECISBP2 Antibody (A06543-4) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-integrin-alpha-4-itga4-picoband-trade-antibody-a00468-3-boster.html2026-03-17T05:13:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00468-3-itga4-primary-antibodies-wb-testing-1.jpgAnti-Integrin Alpha 4/ITGA4 Antibody Picoband® Western blot analysis of Integrin Alpha 4/ITGA4 using anti-Integrin Alpha 4/ITGA4 antibody (A00468-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human HL-60 whole cell lysates, Lane 4: human U87 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Integrin Alpha 4/ITGA4 antigen affinity purified polyclonal antibody (Catalog # A00468-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Integrin Alpha 4/ITGA4 at approximately 140-150 kDa. The expected band size for Integrin Alpha 4/ITGA4 is at 115 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-adgre5-picoband-trade-antibody-a30392-2-boster.html2026-03-17T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30392-2-adgre5-primary-antibodies-wb-testing-1.jpgAnti-ADGRE5 Antibody Picoband® Western blot analysis of ADGRE5 using anti-ADGRE5 antibody (A30392-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADGRE5 antigen affinity purified polyclonal antibody (Catalog # A30392-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADGRE5 at approximately 98 kDa. The expected band size for ADGRE5 is at 92 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a30392-2-adgre5-primary-antibodies-fcm-testing-2.pngAnti-ADGRE5 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-ADGRE5 antibody (A30392-2). Overlay histogram showing U251 cells stained with A30392-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ADGRE5 Antibody (A30392-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ttc36-picoband-trade-antibody-a18139-boster.html2026-03-17T05:15:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18139-ttc36-primary-antibodies-wb-testing-1.jpgAnti-TTC36 Antibody Picoband® Western blot analysis of TTC36 using anti-TTC36 antibody (A18139). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TTC36 antigen affinity purified polyclonal antibody (Catalog # A18139) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TTC36 at approximately 21 kDa. The expected band size for TTC36 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18139-ttc36-primary-antibodies-if-testing-2.jpgAnti-TTC36 Antibody Picoband® IF analysis of TTC36 using anti-TTC36 antibody (A18139) and anti-Beta Tubulin antibody (M01857-3). TTC36 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TTC36 Antibody (A18139) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18139-ttc36-primary-antibodies-fcm-testing-3.pngAnti-TTC36 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-TTC36 antibody (A18139). Overlay histogram showing 293T cells stained with A18139 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TTC36 Antibody (A18139, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-gnai2-picoband-trade-antibody-a02498-3-boster.html2026-03-16T09:42:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-wb-testing-1.jpgAnti-GNAI2 Antibody Picoband® Western blot analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GNAI2 antigen affinity purified polyclonal antibody (Catalog # A02498-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GNAI2 at approximately 40 kDa. The expected band size for GNAI2 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-ihc-testing-2.jpgAnti-GNAI2 Antibody Picoband® IHC analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-ihc-testing-3.jpgAnti-GNAI2 Antibody Picoband® IHC analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-ihc-testing-4.jpgAnti-GNAI2 Antibody Picoband® IHC analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-ihc-testing-5.jpgAnti-GNAI2 Antibody Picoband® IHC analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-ihc-testing-6.jpgAnti-GNAI2 Antibody Picoband® IHC analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-ihc-testing-7.jpgAnti-GNAI2 Antibody Picoband® IHC analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-if-testing-8.jpgAnti-GNAI2 Antibody Picoband® IF analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-if-testing-2.pngAnti-GNAI2 Antibody Picoband® IF analysis of GNAI2 using anti-GNAI2 antibody (A02498-3). GNAI2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-GNAI2 Antibody (A02498-3) overnight at 4°C.Goat Anti-Rabbit IgG (H+L) Secondary Antibody, Fluoro488 Conjugated (BA1127) was used as secondary antibody incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02498-3-gnai2-primary-antibodies-fcm-testing-9.pngAnti-GNAI2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-GNAI2 antibody (A02498-3). Overlay histogram showing HEL cells stained with A02498-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GNAI2 Antibody (A02498-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-aatf-picoband-trade-antibody-a03945-3-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-wb-testing-1.jpgAnti-AATF Antibody Picoband® Western blot analysis of AATF using anti-AATF antibody (A03945-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AATF antigen affinity purified polyclonal antibody (Catalog # A03945-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AATF at approximately 95 kDa. The expected band size for AATF is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-ihc-testing-1.jpgAnti-AATF Antibody Picoband®IHC analysis of AATF using anti-AATF antibody (A03945-3). AATF was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AATF Antibody (A03945-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-ihc-testing-6.jpgAnti-AATF Antibody Picoband®IHC analysis of AATF using anti-AATF antibody (A03945-3). AATF was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AATF Antibody (A03945-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-ihc-testing-2.jpgAnti-AATF Antibody Picoband® IHC analysis of AATF using anti-AATF antibody (A03945-3). AATF was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AATF Antibody (A03945-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-ihc-testing-3.jpgAnti-AATF Antibody Picoband® IHC analysis of AATF using anti-AATF antibody (A03945-3). AATF was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AATF Antibody (A03945-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-ihc-testing-4.jpgAnti-AATF Antibody Picoband® IHC analysis of AATF using anti-AATF antibody (A03945-3). AATF was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AATF Antibody (A03945-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-ihc-testing-5.jpgAnti-AATF Antibody Picoband® IHC analysis of AATF using anti-AATF antibody (A03945-3). AATF was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AATF Antibody (A03945-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-if-testing-6.jpgAnti-AATF Antibody Picoband® IF analysis of AATF using anti-AATF antibody (A03945-3) and anti-Beta Tubulin antibody (M01857-3). AATF was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-AATF Antibody (A03945-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03945-3-aatf-primary-antibodies-if-testing-7.jpgAnti-AATF Antibody Picoband® IF analysis of AATF using anti-AATF antibody (A03945-3). AATF was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-AATF Antibody (A03945-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-ranbp9-picoband-trade-antibody-a03448-1-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03448-1-ranbp9-primary-antibodies-wb-testing-1.jpgAnti-RANBP9 Antibody Picoband® Western blot analysis of RANBP9 using anti-RANBP9 antibody (A03448-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human CCRF-CEM whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RANBP9 antigen affinity purified polyclonal antibody (Catalog # A03448-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RANBP9 at approximately 91 kDa. The expected band size for RANBP9 is at 78 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03448-1-ranbp9-primary-antibodies-if-testing-2.jpgAnti-RANBP9 Antibody Picoband® IF analysis of RANBP9 using anti-RANBP9 antibody (A03448-1) and anti-Beta Tubulin antibody (M01857-3). RANBP9 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RANBP9 Antibody (A03448-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03448-1-ranbp9-primary-antibodies-fcm-testing-3.pngAnti-RANBP9 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-RANBP9 antibody (A03448-1). Overlay histogram showing U20S cells stained with A03448-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RANBP9 Antibody (A03448-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rbpms2-picoband-trade-antibody-a10660-1-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10660-1-rbpms2-primary-antibodies-wb-testing-1.jpgAnti-RBPMS2 Antibody Picoband® Western blot analysis of RBPMS2 using anti-RBPMS2 antibody (A10660-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBPMS2 antigen affinity purified polyclonal antibody (Catalog # A10660-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RBPMS2 at approximately 28 kDa. The expected band size for RBPMS2 is at 22 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-dkk3-rig-picoband-trade-antibody-a03140-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03140-rig-primary-antibodies-wb-testing-1.jpgAnti-DKK3/RIG Antibody Picoband® Western blot analysis of DKK3/RIG using anti-DKK3/RIG antibody (A03140). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: human U-87MG whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DKK3/RIG antigen affinity purified polyclonal antibody (Catalog # A03140) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DKK3/RIG at approximately 22 kDa. The expected band size for DKK3/RIG is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03140-rig-primary-antibodies-if-testing-2.jpgAnti-DKK3/RIG Antibody Picoband® IF analysis of DKK3/RIG using anti-DKK3/RIG antibody (A03140). DKK3/RIG was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DKK3/RIG Antibody (A03140) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03140-rig-primary-antibodies-fcm-testing-3.pngAnti-DKK3/RIG Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-DKK3/RIG antibody (A03140). Overlay histogram showing SH-SY5Y cells stained with A03140 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DKK3/RIG Antibody (A03140, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ranbp3-picoband-trade-antibody-a06252-1-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06252-1-ranbp3-primary-antibodies-wb-testing-1_1.jpgAnti-RANBP3 Antibody Picoband® Western blot analysis of RANBP3 using anti-RANBP3 antibody (A06252-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 1200V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RANBP3 antigen affinity purified polyclonal antibody (Catalog # A06252-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RANBP3 at approximately 70, 90 kDa. The expected band size for RANBP3 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06252-1-ranbp3-primary-antibodies-ihc-testing-2_1.jpgAnti-RANBP3 Antibody Picoband® IHC analysis of RANBP3 using anti-RANBP3 antibody (A06252-1). RANBP3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RANBP3 Antibody (A06252-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06252-1-ranbp3-primary-antibodies-if-testing-3.jpgAnti-RANBP3 Antibody Picoband® IF analysis of RANBP3 using anti-RANBP3 antibody (A06252-1) and anti-Tubulin Alpha antibody (M03989-3). RANBP3 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RANBP3 Antibody (A06252-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06252-1-ranbp3-primary-antibodies-fcm-testing-4.jpgAnti-RANBP3 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-RANBP3 antibody (A06252-1). Overlay histogram showing PC-3 cells stained with A06252-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RANBP3 Antibody (A06252-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-rapgef5-picoband-trade-antibody-a12923-2-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12923-2-rapgef5-primary-antibodies-wb-testing-1.jpgAnti-RAPGEF5 Antibody Picoband® Western blot analysis of RAPGEF5 using anti-RAPGEF5 antibody (A12923-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAPGEF5 antigen affinity purified polyclonal antibody (Catalog # A12923-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAPGEF5 at approximately 75 kDa. The expected band size for RAPGEF5 is at 68 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-rassf7-picoband-trade-antibody-a09402-2-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09402-2-rassf7-primary-antibodies-wb-testing-1.jpgAnti-RASSF7 Antibody Picoband® Western blot analysis of RASSF7 using anti-RASSF7 antibody (A09402-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HL-60 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RASSF7 antigen affinity purified polyclonal antibody (Catalog # A09402-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RASSF7 at approximately 37 kDa. The expected band size for RASSF7 is at 40 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-rassf8-picoband-trade-antibody-a11627-1-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11627-1-rassf8-primary-antibodies-wb-testing-1.jpgAnti-RASSF8 Antibody Picoband® Western blot analysis of RASSF8 using anti-RASSF8 antibody (A11627-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human placenta tissue lysates, Lane 4: human U251 whole cell lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RASSF8 antigen affinity purified polyclonal antibody (Catalog # A11627-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RASSF8 at approximately 48 kDa. The expected band size for RASSF8 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11627-1-rassf8-primary-antibodies-ihc-testing-1.jpgAnti-RASSF8 Antibody Picoband®IHC analysis of RASSF8 using anti-RASSF8 antibody (A11627-1). RASSF8 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RASSF8 Antibody (A11627-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11627-1-rassf8-primary-antibodies-if-testing-2.jpgAnti-RASSF8 Antibody Picoband® IF analysis of RASSF8 using anti-RASSF8 antibody (A11627-1). RASSF8 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RASSF8 Antibody (A11627-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11627-1-rassf8-primary-antibodies-fcm-testing-3.pngAnti-RASSF8 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-RASSF8 antibody (A11627-1). Overlay histogram showing PC-3 cells stained with A11627-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RASSF8 Antibody (A11627-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rbbp8-picoband-trade-antibody-a02076-2-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02076-2-rbbp8-primary-antibodies-wb-testing-1.jpgAnti-RBBP8 Antibody Picoband® Western blot analysis of RBBP8 using anti-RBBP8 antibody (A02076-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBBP8 antigen affinity purified polyclonal antibody (Catalog # A02076-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RBBP8 at approximately 130 kDa. The expected band size for RBBP8 is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02076-2-rbbp8-primary-antibodies-ihc-testing-2.jpgAnti-RBBP8 Antibody Picoband® IHC analysis of RBBP8 using anti-RBBP8 antibody (A02076-2). RBBP8 was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBBP8 Antibody (A02076-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02076-2-rbbp8-primary-antibodies-ihc-testing-3.jpgAnti-RBBP8 Antibody Picoband® IHC analysis of RBBP8 using anti-RBBP8 antibody (A02076-2). RBBP8 was detected in a paraffin-embedded section of human mucinous adenoma of ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBBP8 Antibody (A02076-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02076-2-rbbp8-primary-antibodies-ihc-testing-4.jpgAnti-RBBP8 Antibody Picoband® IHC analysis of RBBP8 using anti-RBBP8 antibody (A02076-2). RBBP8 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBBP8 Antibody (A02076-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02076-2-rbbp8-primary-antibodies-if-testing-5.jpgAnti-RBBP8 Antibody Picoband® IF analysis of RBBP8 using anti-RBBP8 antibody (A02076-2) and anti-Beta Tubulin antibody (M01857-3). RBBP8 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RBBP8 Antibody (A02076-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02076-2-rbbp8-primary-antibodies-fcm-testing-6.pngAnti-RBBP8 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-RBBP8 antibody (A02076-2). Overlay histogram showing MCF-7 cells stained with A02076-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RBBP8 Antibody (A02076-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rbm12b-picoband-trade-antibody-a14571-1-boster.html2026-03-17T05:15:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14571-1-rbm12b-primary-antibodies-wb-testing-1.jpgAnti-RBM12B Antibody Picoband® Western blot analysis of RBM12B using anti-RBM12B antibody (A14571-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBM12B antigen affinity purified polyclonal antibody (Catalog # A14571-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RBM12B at approximately 130 kDa. The expected band size for RBM12B is at 118 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14571-1-rbm12b-primary-antibodies-if-testing-2.jpgAnti-RBM12B Antibody Picoband® IF analysis of RBM12B using anti-RBM12B antibody (A14571-1) and anti-Beta Tubulin antibody (M01857-3). RBM12B was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RBM12B Antibody (A14571-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14571-1-rbm12b-primary-antibodies-ip-testing-1.jpgAnti-RBM12B Antibody Picoband®Immunoprecipitating (IP) RBM12B in A431 whole cell lysate. Western blot analysis of RBM12B using anti-RBM12B antibody (A14571-1); Lane 1: A431 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-RBM12B antibody in A431 whole cell lysate; Lane 3: anti-RBM12B antibody (2μg) + A431 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RBM12B antigen affinity purified polyclonal antibody (A14571-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for RBM12B at approximately 130 kDa. The expected band size for RBM12B is at 118 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14571-1-rbm12b-primary-antibodies-fcm-testing-3.pngAnti-RBM12B Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-RBM12B antibody (A14571-1). Overlay histogram showing A431 cells stained with A14571-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RBM12B Antibody (A14571-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14571-1-rbm12b-primary-antibodies-fcm-testing-4.pngAnti-RBM12B Antibody Picoband® Flow Cytometry analysis of JK cells using anti-RBM12B antibody (A14571-1). Overlay histogram showing JK cells stained with A14571-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RBM12B Antibody (A14571-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rbm42-picoband-trade-antibody-a14229-1-boster.html2026-03-17T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-wb-testing-1.jpgAnti-RBM42 Antibody Picoband® Western blot analysis of RBM42 using anti-RBM42 antibody (A14229-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBM42 antigen affinity purified polyclonal antibody (Catalog # A14229-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RBM42 at approximately 65 kDa. The expected band size for RBM42 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-ihc-testing-2.jpgAnti-RBM42 Antibody Picoband® IHC analysis of RBM42 using anti-RBM42 antibody (A14229-1). RBM42 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBM42 Antibody (A14229-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-ihc-testing-3.jpgAnti-RBM42 Antibody Picoband® IHC analysis of RBM42 using anti-RBM42 antibody (A14229-1). RBM42 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBM42 Antibody (A14229-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-ihc-testing-4..jpgAnti-RBM42 Antibody Picoband® IHC analysis of RBM42 using anti-RBM42 antibody (A14229-1). RBM42 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBM42 Antibody (A14229-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-ihc-testing-5.jpgAnti-RBM42 Antibody Picoband® IHC analysis of RBM42 using anti-RBM42 antibody (A14229-1). RBM42 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBM42 Antibody (A14229-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-ihc-testing-6.jpgAnti-RBM42 Antibody Picoband® IHC analysis of RBM42 using anti-RBM42 antibody (A14229-1). RBM42 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBM42 Antibody (A14229-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-if-testing-7.jpgAnti-RBM42 Antibody Picoband® IF analysis of RBM42 using anti-RBM42 antibody (A14229-1) and anti-Beta Tubulin antibody (M01857-3). RBM42 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RBM42 Antibody (A14229-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14229-1-rbm42-primary-antibodies-fcm-testing-8.pngAnti-RBM42 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-RBM42 antibody (A14229-1). Overlay histogram showing 293T cells stained with A14229-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RBM42 Antibody (A14229-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-reck-picoband-trade-antibody-a06439-4-boster.html2026-03-16T09:42:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06439-4-reck-primary-antibodies-wb-testing-1.jpgAnti-RECK Antibody Picoband® Western blot analysis of RECK using anti-RECK antibody (A06439-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse LLC whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RECK antigen affinity purified polyclonal antibody (Catalog # A06439-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RECK at approximately 100 kDa. The expected band size for RECK is at 106 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06439-4-reck-primary-antibodies-fcm-testing-2.pngAnti-RECK Antibody Picoband® Flow Cytometry analysis of JK cells using anti-RECK antibody (A06439-4). Overlay histogram showing JK cells stained with A06439-4 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RECK Antibody (A06439-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rgl3-picoband-trade-antibody-a11774-1-boster.html2026-03-17T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11774-1-rgl3-primary-antibodies-wb-testing-1.jpgAnti-RGL3 Antibody Picoband® Western blot analysis of RGL3 using anti-RGL3 antibody (A11774-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RGL3 antigen affinity purified polyclonal antibody (Catalog # A11774-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RGL3 at approximately 72 kDa. The expected band size for RGL3 is at 78 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11774-1-rgl3-primary-antibodies-ihc-testing-2.jpgAnti-RGL3 Antibody Picoband® IHC analysis of RGL3 using anti-RGL3 antibody (A11774-1). RGL3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RGL3 Antibody (A11774-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11774-1-rgl3-primary-antibodies-ihc-testing-3.jpgAnti-RGL3 Antibody Picoband® IHC analysis of RGL3 using anti-RGL3 antibody (A11774-1). RGL3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RGL3 Antibody (A11774-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11774-1-rgl3-primary-antibodies-if-testing-4.jpgAnti-RGL3 Antibody Picoband® IF analysis of RGL3 using anti-RGL3 antibody (A11774-1) and anti-Beta Tubulin antibody (M01857-3). RGL3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RGL3 Antibody (A11774-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11774-1-rgl3-primary-antibodies-fcm-testing-5.pngAnti-RGL3 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-RGL3 antibody (A11774-1). Overlay histogram showing SH-SY5Y cells stained with A11774-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RGL3 Antibody (A11774-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rnf25-picoband-trade-antibody-a10595-3-boster.html2026-03-17T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-wb-testing-1.jpgAnti-RNF25 Antibody Picoband® Western blot analysis of RNF25 using anti-RNF25 antibody (A10595-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RNF25 antigen affinity purified polyclonal antibody (Catalog # A10595-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RNF25 at approximately 62 kDa. The expected band size for RNF25 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-2.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-3.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-4.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-5.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-6.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-7.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-8_1.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-9.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human urothelial carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-10.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-ihc-testing-11.jpgAnti-RNF25 Antibody Picoband® IHC analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-fcm-testing-12.pngAnti-RNF25 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-RNF25 antibody (A10595-3). Overlay histogram showing 293T cells stained with A10595-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RNF25 Antibody (A10595-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10595-3-rnf25-primary-antibodies-if-testing-13.jpgAnti-RNF25 Antibody Picoband® IF analysis of RNF25 using anti-RNF25 antibody (A10595-3). RNF25 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-RNF25 Antibody (A10595-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-rpl14-picoband-trade-antibody-a07781-2-boster.html2026-03-17T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07781-2-rpl14-primary-antibodies-wb-testing-1.jpgAnti-RPL14 Antibody Picoband® Western blot analysis of RPL14 using anti-RPL14 antibody (A07781-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPL14 antigen affinity purified polyclonal antibody (Catalog # A07781-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPL14 at approximately 26 kDa. The expected band size for RPL14 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07781-2-rpl14-primary-antibodies-if-testing-2.jpgAnti-RPL14 Antibody Picoband® IF analysis of RPL14 using anti-RPL14 antibody (A07781-2). RPL14 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RPL14 Antibody (A07781-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07781-2-rpl14-primary-antibodies-fcm-testing-3.pngAnti-RPL14 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-RPL14 antibody (A07781-2). Overlay histogram showing 293T cells stained with A07781-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPL14 Antibody (A07781-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-prag1-picoband-trade-antibody-a32113-boster.html2026-03-17T05:15:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32113-prag1-primary-antibodies-wb-testing-1.jpgAnti-PRAG1 Antibody Picoband® Western blot analysis of PRAG1 using anti-PRAG1 antibody (A32113). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRAG1 antigen affinity purified polyclonal antibody (Catalog # A32113) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PRAG1 at approximately 200 kDa. The expected band size for PRAG1 is at 150 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32113-prag1-primary-antibodies-if-testing-2.jpgAnti-PRAG1 Antibody Picoband® IF analysis of PRAG1 using anti-PRAG1 antibody (A32113). PRAG1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PRAG1 Antibody (A32113) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32113-prag1-primary-antibodies-fcm-testing-3.pngAnti-PRAG1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PRAG1 antibody (A32113). Overlay histogram showing HepG2 cells stained with A32113 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PRAG1 Antibody (A32113, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nr1d2-picoband-trade-antibody-a04958-2-boster.html2026-03-16T09:42:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04958-2-nr1d2-primary-antibodies-wb-testing-1.jpgAnti-NR1D2 Antibody Picoband® Western blot analysis of NR1D2 using anti-NR1D2 antibody (A04958-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR1D2 antigen affinity purified polyclonal antibody (Catalog # A04958-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NR1D2 at approximately 68 kDa. The expected band size for NR1D2 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04958-2-nr1d2-primary-antibodies-ihc-testing-2.jpgAnti-NR1D2 Antibody Picoband® IHC analysis of NR1D2 using anti-NR1D2 antibody (A04958-2). NR1D2 was detected in a paraffin-embedded section of human cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR1D2 Antibody (A04958-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04958-2-nr1d2-primary-antibodies-ihc-testing-3.jpgAnti-NR1D2 Antibody Picoband® IHC analysis of NR1D2 using anti-NR1D2 antibody (A04958-2). NR1D2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NR1D2 Antibody (A04958-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04958-2-nr1d2-primary-antibodies-fcm-testing-4.pngAnti-NR1D2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-NR1D2 antibody (A04958-2). Overlay histogram showing HepG2 cells stained with A04958-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NR1D2 Antibody (A04958-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04958-2-nr1d2-primary-antibodies-fcm-testing-5.pngAnti-NR1D2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-NR1D2 antibody (A04958-2). Overlay histogram showing JK cells stained with A04958-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NR1D2 Antibody (A04958-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nsmce4a-picoband-trade-antibody-a14289-1-boster.html2026-03-17T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14289-1-nsmce4a-primary-antibodies-wb-testing-1.jpgAnti-NSMCE4A Antibody Picoband® Western blot analysis of NSMCE4A using anti-NSMCE4A antibody (A14289-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat ovary tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse ovary tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSMCE4A antigen affinity purified polyclonal antibody (Catalog # A14289-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSMCE4A at approximately 50 kDa. The expected band size for NSMCE4A is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14289-1-nsmce4a-primary-antibodies-if-testing-2.jpgAnti-NSMCE4A Antibody Picoband® IF analysis of NSMCE4A using anti-NSMCE4A antibody (A14289-1) and anti-Beta Tubulin antibody (M01857-3). NSMCE4A was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NSMCE4A Antibody (A14289-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14289-1-nsmce4a-primary-antibodies-fcm-testing-3.pngAnti-NSMCE4A Antibody Picoband® Flow Cytometry analysis of JK cells using anti-NSMCE4A antibody (A14289-1). Overlay histogram showing JK cells stained with A14289-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NSMCE4A Antibody (A14289-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nup43-picoband-trade-antibody-a11950-1-boster.html2026-03-17T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-wb-testing-1.jpgAnti-NUP43 Antibody Picoband® Western blot analysis of NUP43 using anti-NUP43 antibody (A11950-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP43 antigen affinity purified polyclonal antibody (Catalog # A11950-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP43 at approximately 42 kDa. The expected band size for NUP43 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-2.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-3.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-4.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-5.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-6.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-7.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-8.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-9.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-10.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-11.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-12.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-13.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-14.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-15.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-16.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-17.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-18.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-19.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-20.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-ihc-testing-21.jpgAnti-NUP43 Antibody Picoband® IHC analysis of NUP43 using anti-NUP43 antibody (A11950-1). NUP43 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUP43 Antibody (A11950-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-if-testing-22.jpgAnti-NUP43 Antibody Picoband® IF analysis of NUP43 using anti-NUP43 antibody (A11950-1) and anti-Beta Tubulin antibody (M01857-3). NUP43 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP43 Antibody (A11950-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11950-1-nup43-primary-antibodies-fcm-testing-23.pngAnti-NUP43 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-NUP43 antibody (A11950-1). Overlay histogram showing K562 cells stained with A11950-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUP43 Antibody (A11950-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-nup98-picoband-trade-antibody-a01301-1-boster.html2026-03-17T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01301-1-nup98-primary-antibodies-wb-testing-1.jpgAnti-NUP98 Antibody Picoband® Western blot analysis of NUP98 using anti-NUP98 antibody (A01301-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat NRK whole cell lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUP98 antigen affinity purified polyclonal antibody (Catalog # A01301-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUP98 at approximately 98,105 kDa. The expected band size for NUP98 is at 198 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01301-1-nup98-primary-antibodies-if-testing-2.jpgAnti-NUP98 Antibody Picoband® IF analysis of NUP98 using anti-NUP98 antibody (A01301-1). NUP98 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUP98 Antibody (A01301-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01301-1-nup98-primary-antibodies-fcm-testing-3.pngAnti-NUP98 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-NUP98 antibody (A01301-1). Overlay histogram showing K562 cells stained with A01301-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUP98 Antibody (A01301-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mamdc4-picoband-trade-antibody-a16484-boster.html2026-03-17T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16484-mamdc4-primary-antibodies-wb-testing-1.jpgAnti-MAMDC4 Antibody Picoband® Western blot analysis of MAMDC4 using anti-MAMDC4 antibody (A16484). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse thymus tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAMDC4 antigen affinity purified polyclonal antibody (Catalog # A16484) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAMDC4 at approximately 100 kDa. The expected band size for MAMDC4 is at 131 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16484-mamdc4-primary-antibodies-if-testing-2.jpgAnti-MAMDC4 Antibody Picoband® IF analysis of MAMDC4 using anti-MAMDC4 antibody (A16484). MAMDC4 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAMDC4 Antibody (A16484) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16484-mamdc4-primary-antibodies-fcm-testing-3.pngAnti-MAMDC4 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MAMDC4 antibody (A16484). Overlay histogram showing HepG2 cells stained with A16484 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MAMDC4 Antibody (A16484, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-map4k3-picoband-trade-antibody-a07188-2-boster.html2026-03-17T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07188-2-map4k3-primary-antibodies-wb-testing-1.jpgAnti-MAP4K3 Antibody Picoband® Western blot analysis of MAP4K3 using anti-MAP4K3 antibody (A07188-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U-87MG whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP4K3 antigen affinity purified polyclonal antibody (Catalog # A07188-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAP4K3 at approximately 100 kDa. The expected band size for MAP4K3 is at 101 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07188-2-map4k3-primary-antibodies-ihc-testing-2.jpgAnti-MAP4K3 Antibody Picoband® IHC analysis of MAP4K3 using anti-MAP4K3 antibody (A07188-2). MAP4K3 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP4K3 Antibody (A07188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07188-2-map4k3-primary-antibodies-ihc-testing-3.jpgAnti-MAP4K3 Antibody Picoband® IHC analysis of MAP4K3 using anti-MAP4K3 antibody (A07188-2). MAP4K3 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP4K3 Antibody (A07188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07188-2-map4k3-primary-antibodies-ihc-testing-4.jpgAnti-MAP4K3 Antibody Picoband® IHC analysis of MAP4K3 using anti-MAP4K3 antibody (A07188-2). MAP4K3 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP4K3 Antibody (A07188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07188-2-map4k3-primary-antibodies-ihc-testing-5.jpgAnti-MAP4K3 Antibody Picoband® IHC analysis of MAP4K3 using anti-MAP4K3 antibody (A07188-2). MAP4K3 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP4K3 Antibody (A07188-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07188-2-map4k3-primary-antibodies-fcm-testing-6.pngAnti-MAP4K3 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MAP4K3 antibody (A07188-2). Overlay histogram showing 293T cells stained with A07188-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAP4K3 Antibody (A07188-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-maz-picoband-trade-antibody-a05631-2-boster.html2026-03-16T09:42:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05631-2-maz-primary-antibodies-wb-testing-1.jpgAnti-MAZ Antibody Picoband® Western blot analysis of MAZ using anti-MAZ antibody (A05631-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAZ antigen affinity purified polyclonal antibody (Catalog # A05631-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAZ at approximately 55 kDa. The expected band size for MAZ is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05631-2-maz-primary-antibodies-if-testing-2.jpgAnti-MAZ Antibody Picoband® IF analysis of MAZ using anti-MAZ antibody (A05631-2) and anti-Beta Tubulin antibody (M01857-3). MAZ was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAZ Antibody (A05631-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05631-2-maz-primary-antibodies-fcm-testing-3.pngAnti-MAZ Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MAZ antibody (A05631-2). Overlay histogram showing HepG2 cells stained with A05631-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAZ Antibody (A05631-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-mbd4-picoband-trade-antibody-a03462-1-boster.html2026-03-17T05:15:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03462-1-mbd4-primary-antibodies-wb-testing-1.jpgAnti-Mbd4 Antibody Picoband® Western blot analysis of Mbd4 using anti-Mbd4 antibody (A03462-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Mbd4 antigen affinity purified polyclonal antibody (Catalog # A03462-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Mbd4 at approximately 66 kDa. The expected band size for Mbd4 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03462-1-mbd4-primary-antibodies-fcm-testing-2.pngAnti-Mbd4 Antibody Picoband® Flow Cytometry analysis of C2C12 cells using anti-Mbd4 antibody (A03462-1). Overlay histogram showing C2C12 cells stained with A03462-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Mbd4 Antibody (A03462-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-ganp-mcm3ap-picoband-trade-antibody-a05445-2-boster.html2026-03-16T09:42:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05445-2-mcm3ap-primary-antibodies-wb-testing-1.jpgAnti-GANP/MCM3AP Antibody Picoband® Western blot analysis of GANP/MCM3AP using anti-GANP/MCM3AP antibody (A05445-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GANP/MCM3AP antigen affinity purified polyclonal antibody (Catalog # A05445-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GANP/MCM3AP at approximately 218 kDa. The expected band size for GANP/MCM3AP is at 218 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05445-2-mcm3ap-primary-antibodies-if-testing-2.jpgAnti-GANP/MCM3AP Antibody Picoband® IF analysis of GANP/MCM3AP using anti-GANP/MCM3AP antibody (A05445-2) and anti-Beta Tubulin antibody (M01857-3). GANP/MCM3AP was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GANP/MCM3AP Antibody (A05445-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05445-2-mcm3ap-primary-antibodies-fcm-testing-3.pngAnti-GANP/MCM3AP Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-GANP/MCM3AP antibody (A05445-2). Overlay histogram showing HEL cells stained with A05445-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GANP/MCM3AP Antibody (A05445-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-orc2-picoband-trade-antibody-a04350-1-boster.html2026-03-17T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-wb-testing-1.jpgAnti-ORC2 Antibody Picoband® Western blot analysis of ORC2 using anti-ORC2 antibody (A04350-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human A2780 whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ORC2 antigen affinity purified polyclonal antibody (Catalog # A04350-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ORC2 at approximately 74 kDa. The expected band size for ORC2 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-wb-testing-2.jpgAnti-ORC2 Antibody Picoband® Western blot analysis of ORC2 using anti-ORC2 antibody (A04350-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ORC2 antigen affinity purified polyclonal antibody (Catalog # A04350-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ORC2 at approximately 74 kDa. The expected band size for ORC2 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-ihc-testing-3.jpgAnti-ORC2 Antibody Picoband® IHC analysis of ORC2 using anti-ORC2 antibody (A04350-1). ORC2 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ORC2 Antibody (A04350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-ihc-testing-4.jpgAnti-ORC2 Antibody Picoband® IHC analysis of ORC2 using anti-ORC2 antibody (A04350-1). ORC2 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ORC2 Antibody (A04350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-ihc-testing-5.jpgAnti-ORC2 Antibody Picoband® IHC analysis of ORC2 using anti-ORC2 antibody (A04350-1). ORC2 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ORC2 Antibody (A04350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-ihc-testing-6.jpgAnti-ORC2 Antibody Picoband® IHC analysis of ORC2 using anti-ORC2 antibody (A04350-1). ORC2 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ORC2 Antibody (A04350-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-if-testing-7.jpgAnti-ORC2 Antibody Picoband® IF analysis of ORC2 using anti-ORC2 antibody (A04350-1) and anti-Beta Tubulin antibody (M01857-3). ORC2 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ORC2 Antibody (A04350-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04350-1-orc2-primary-antibodies-fcm-testing-8.pngAnti-ORC2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ORC2 antibody (A04350-1). Overlay histogram showing HepG2 cells stained with A04350-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ORC2 Antibody (A04350-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-cyp1b1-picoband-trade-antibody-a00515-boster.html2026-03-16T09:42:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00515-cyp1b1-primary-antibodies-wb-testing-1.jpgAnti-CYP1B1 Antibody Picoband® Western blot analysis of CYP1B1 using anti-CYP1B1 antibody (A00515). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: mouse Neuro-2a whole cell lysates, Lane 3: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYP1B1 antigen affinity purified polyclonal antibody (Catalog # A00515) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CYP1B1 at approximately 52 kDa. The expected band size for CYP1B1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00515-cyp1b1-primary-antibodies-fcm-testing-2.pngAnti-CYP1B1 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-CYP1B1 antibody (A00515). Overlay histogram showing THP-1 cells stained with A00515 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CYP1B1 Antibody (A00515, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rbm17-picoband-trade-antibody-a08621-1-boster.html2026-03-17T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08621-1-rbm17-primary-antibodies-wb-testing-1.jpgAnti-RBM17 Antibody Picoband® Western blot analysis of RBM17 using anti-RBM17 antibody (A08621-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RBM17 antigen affinity purified polyclonal antibody (Catalog # A08621-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RBM17 at approximately 45 kDa. The expected band size for RBM17 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08621-1-rbm17-primary-antibodies-ihc-testing-1.jpgAnti-RBM17 Antibody Picoband®IHC analysis of RBM17 using anti-RBM17 antibody (A08621-1). RBM17 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RBM17 Antibody (A08621-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08621-1-rbm17-primary-antibodies-fcm-testing-2.pngAnti-RBM17 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-RBM17 antibody (A08621-1). Overlay histogram showing PC-3 cells stained with A08621-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RBM17 Antibody (A08621-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08621-1-rbm17-primary-antibodies-if-testing-1.jpgAnti-RBM17 Antibody Picoband®IF analysis of RBM17 using anti-RBM17 antibody (A08621-1) and anti-Tubulin Alpha antibody (M03989-3). RBM17 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RBM17 Antibody (A08621-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-ring1-picoband-trade-antibody-a01824-2-boster.html2026-03-17T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01824-2-ring1-primary-antibodies-wb-testing-1.jpgAnti-RING1 Antibody Picoband® Western blot analysis of RING1 using anti-RING1 antibody (A01824-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat PC-12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RING1 antigen affinity purified polyclonal antibody (Catalog # A01824-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RING1 at approximately 50 kDa. The expected band size for RING1 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01824-2-ring1-primary-antibodies-if-testing-2.jpgAnti-RING1 Antibody Picoband® IF analysis of RING1 using anti-RING1 antibody (A01824-2) and anti-Beta Tubulin antibody (M01857-3). RING1 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RING1 Antibody (A01824-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and FITC Conjugated Goat Anti-Mouse IgG (BA1101) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01824-2-ring1-primary-antibodies-fcm-testing-3.pngAnti-RING1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-RING1 antibody (A01824-2). Overlay histogram showing JK cells stained with A01824-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RING1 Antibody (A01824-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rfx4-picoband-trade-antibody-a08516-2-boster.html2026-03-17T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08516-2-rfx4-primary-antibodies-wb-testing-1.jpgAnti-RFX4 Antibody Picoband® Western blot analysis of RFX4 using anti-RFX4 antibody (A08516-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RFX4 antigen affinity purified polyclonal antibody (Catalog # A08516-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RFX4 at approximately 90 kDa. The expected band size for RFX4 is at 83 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-rpap3-picoband-trade-antibody-a03391-1-boster.html2026-03-17T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03391-1-rpap3-primary-antibodies-wb-testing-1.jpgAnti-RPAP3 Antibody Picoband® Western blot analysis of RPAP3 using anti-RPAP3 antibody (A03391-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPAP3 antigen affinity purified polyclonal antibody (Catalog # A03391-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPAP3 at approximately 76 kDa. The expected band size for RPAP3 is at 76 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-rsl24d1-picoband-trade-antibody-a14856-1-boster.html2026-03-17T05:15:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14856-1-rsl24d1-primary-antibodies-wb-testing-1.jpgAnti-RSL24D1 Antibody Picoband® Western blot analysis of RSL24D1 using anti-RSL24D1 antibody (A14856-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human HL-60 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human MOLT-4 whole cell lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse SP2/0 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RSL24D1 antigen affinity purified polyclonal antibody (Catalog # A14856-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RSL24D1 at approximately 20 kDa. The expected band size for RSL24D1 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14856-1-rsl24d1-primary-antibodies-if-testing-2.jpgAnti-RSL24D1 Antibody Picoband® IF analysis of RSL24D1 using anti-RSL24D1 antibody (A14856-1). RSL24D1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RSL24D1 Antibody (A14856-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14856-1-rsl24d1-primary-antibodies-fcm-testing-3.pngAnti-RSL24D1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-RSL24D1 antibody (A14856-1). Overlay histogram showing JK cells stained with A14856-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RSL24D1 Antibody (A14856-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-rspo4-picoband-trade-antibody-a09583-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09583-rpso4-primary-antibodies-wb-testing-1.jpgAnti-RSPO4 Antibody Picoband® Western blot analysis of RSPO4 using anti-RSPO4 antibody (A09583). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RSPO4 antigen affinity purified polyclonal antibody (Catalog # A09583) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RSPO4 at approximately 26 kDa. The expected band size for RSPO4 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09583-rpso4-primary-antibodies-fcm-testing-2.pngAnti-RSPO4 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-RSPO4 antibody (A09583). Overlay histogram showing 293T cells stained with A09583 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RSPO4 Antibody (A09583, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-osm-picoband-trade-antibody-a00804-3-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00804-3-osm-primary-antibodies-wb-testing-1.jpgAnti-Osm Antibody Picoband® Western blot analysis of Osm using anti-Osm antibody (A00804-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse tetis tissue lysates, Lane 5: mouse kidney tissue lysates, Lane 6: mouse lung tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Osm antigen affinity purified polyclonal antibody (Catalog # A00804-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Osm at approximately 27 kDa. The expected band size for Osm is at 27 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-palladin-palld-picoband-trade-antibody-a04005-3-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04005-3-palld-primary-antibodies-wb-testing-1.jpgAnti-Palladin/PALLD Antibody Picoband® Western blot analysis of Palladin/PALLD using anti-Palladin/PALLD antibody (A04005-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Palladin/PALLD antigen affinity purified polyclonal antibody (Catalog # A04005-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Palladin/PALLD at approximately 95 kDa. The expected band size for Palladin/PALLD is at 151 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-parvg-picoband-trade-antibody-a11061-1-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11061-1-parvg-primary-antibodies-wb-testing-1.jpgAnti-PARVG Antibody Picoband® Western blot analysis of PARVG using anti-PARVG antibody (A11061-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HEL1 whole cell lysates, Lane 3: rat thymus tissue lysates, Lane 4: mouse thymus tissue lysates, Lane 5: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARVG antigen affinity purified polyclonal antibody (Catalog # A11061-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARVG at approximately 37 kDa. The expected band size for PARVG is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11061-1-parvg-primary-antibodies-fcm-testing-2.pngAnti-PARVG Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PARVG antibody (A11061-1). Overlay histogram showing JK cells stained with A11061-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PARVG Antibody (A11061-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pax8-picoband-trade-antibody-a00943-4-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00943-4-pax8-primary-antibodies-wb-testing-1.jpgAnti-PAX8 Antibody Picoband® Western blot analysis of PAX8 using anti-PAX8 antibody (A00943-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SW579 whole cell lysates, Lane 2: human SK-OV-3 whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat NRK whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAX8 antigen affinity purified polyclonal antibody (Catalog # A00943-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PAX8 at approximately 48 kDa. The expected band size for PAX8 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00943-4-pax8-primary-antibodies-if-testing-2.jpgAnti-PAX8 Antibody Picoband® IF analysis of PAX8 using anti-PAX8 antibody (A00943-4) and anti-Beta Tubulin antibody (M01857-3). PAX8 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PAX8 Antibody (A00943-4) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-pcbd1-picoband-trade-antibody-a07264-1-boster.html2026-03-16T09:42:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07264-1-pcbd1-primary-antibodies-wb-testing-1.jpgAnti-PCBD1 Antibody Picoband® Western blot analysis of PCBD1 using anti-PCBD1 antibody (A07264-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: mouse pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCBD1 antigen affinity purified polyclonal antibody (Catalog # A07264-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCBD1 at approximately 12 kDa. The expected band size for PCBD1 is at 12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07264-1-pcbd1-primary-antibodies-if-testing-2.jpgAnti-PCBD1 Antibody Picoband® IF analysis of PCBD1 using anti-PCBD1 antibody (A07264-1) and anti-Beta Tubulin antibody (M01857-3). PCBD1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PCBD1 Antibody (A07264-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-acvr2a-picoband-trade-antibody-a04770-2-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04770-2-acvr2a-primary-antibodies-wb-testing-1.jpgAnti-ACVR2A Antibody Picoband® Western blot analysis of ACVR2A using anti-ACVR2A antibody (A04770-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACVR2A antigen affinity purified polyclonal antibody (Catalog # A04770-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACVR2A at approximately 58 kDa. The expected band size for ACVR2A is at 58 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-aqp2-picoband-trade-antibody-a00935-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00935-aqp2-primary-antibodies-wb-testing-1.jpgAnti-Aqp2 Antibody Picoband® Western blot analysis of Aqp2 using anti-Aqp2 antibody (A00935). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Aqp2 antigen affinity purified polyclonal antibody (Catalog # A00935) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Aqp2 at approximately 26 kDa. The expected band size for Aqp2 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00935-aqp2-primary-antibodies-fcm-testing-2.pngAnti-Aqp2 Antibody Picoband® Flow Cytometry analysis of RAW264.7 cells using anti-Aqp2 antibody (A00935). Overlay histogram showing RAW264.7 cells stained with A00935 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Aqp2 Antibody (A00935, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pde8a-picoband-trade-antibody-a05304-1-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05304-1-pde8a-primary-antibodies-wb-testing-1.jpgAnti-PDE8A Antibody Picoband® Western blot analysis of PDE8A using anti-PDE8A antibody (A05304-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDE8A antigen affinity purified polyclonal antibody (Catalog # A05304-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDE8A at approximately 93 kDa. The expected band size for PDE8A is at 93 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05304-1-pde8a-primary-antibodies-fcm-testing-2.pngAnti-PDE8A Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PDE8A antibody (A05304-1). Overlay histogram showing SH-SY5Y cells stained with A05304-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDE8A Antibody (A05304-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pdpr-picoband-trade-antibody-a12185-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12185-pdpr-primary-antibodies-wb-testing-1.jpgAnti-PDPR Antibody Picoband® Western blot analysis of PDPR using anti-PDPR antibody (A12185). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDPR antigen affinity purified polyclonal antibody (Catalog # A12185) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDPR at approximately 99 kDa. The expected band size for PDPR is at 99 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12185-pdpr-primary-antibodies-fcm-testing-2.pngAnti-PDPR Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PDPR antibody (A12185). Overlay histogram showing JK cells stained with A12185 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDPR Antibody (A12185, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pepd-picoband-trade-antibody-a03417-1-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03417-1-pepd-primary-antibodies-wb-testing-1.jpgAnti-PEPD Antibody Picoband® Western blot analysis of PEPD using anti-PEPD antibody (A03417-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat small intestine tissue lysates, Lane 6: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PEPD antigen affinity purified polyclonal antibody (Catalog # A03417-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PEPD at approximately 60 kDa. The expected band size for PEPD is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03417-1-pepd-primary-antibodies-if-testing-2.jpgAnti-PEPD Antibody Picoband® IF analysis of PEPD using anti-PEPD antibody (A03417-1) and anti-Beta Tubulin antibody (M01857-3). PEPD was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PEPD Antibody (A03417-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03417-1-pepd-primary-antibodies-fcm-testing-3.pngAnti-PEPD Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PEPD antibody (A03417-1). Overlay histogram showing 293T cells stained with A03417-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PEPD Antibody (A03417-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-plekhb1-picoband-trade-antibody-a11037-1-boster.html2026-03-16T09:42:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11037-1-plekhb1-primary-antibodies-wb-testing-1.jpgAnti-PLEKHB1 Antibody Picoband® Western blot analysis of PLEKHB1 using anti-PLEKHB1 antibody (A11037-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: monkey RF/6A whole cell lysates, Lane 5: rat eye tissue lysates, Lane 6: mouse eye tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLEKHB1 antigen affinity purified polyclonal antibody (Catalog # A11037-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLEKHB1 at approximately 27 kDa. The expected band size for PLEKHB1 is at 27 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-pfkfb4-picoband-trade-antibody-a07028-1-boster.html2026-03-17T05:15:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07028-1-pfkfb4-primary-antibodies-wb-testing-1.jpgAnti-PFKFB4 Antibody Picoband® Western blot analysis of PFKFB4 using anti-PFKFB4 antibody (A07028-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PFKFB4 antigen affinity purified polyclonal antibody (Catalog # A07028-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PFKFB4 at approximately 54 kDa. The expected band size for PFKFB4 is at 54 kDa. https://www.bosterbio.com/products/primary-antibodies/anti-pmm2-picoband-trade-antibody-a03146-1-boster.html2026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03146-1-pmm2-primary-antibodies-wb-testing-1.jpgAnti-PMM2 Antibody Picoband® Western blot analysis of PMM2 using anti-PMM2 antibody (A03146-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat small intestines tissue lysates, Lane 5: mouse small intestines tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PMM2 antigen affinity purified polyclonal antibody (Catalog # A03146-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PMM2 at approximately 28 kDa. The expected band size for PMM2 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03146-1-pmm2-primary-antibodies-if-testing-2.jpgAnti-PMM2 Antibody Picoband® IF analysis of PMM2 using anti-PMM2 antibody (A03146-1) and anti-Beta Tubulin antibody (M01857-3). PMM2 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PMM2 Antibody (A03146-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03146-1-pmm2-primary-antibodies-fcm-testing-3.pngAnti-PMM2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-PMM2 antibody (A03146-1). Overlay histogram showing HEL cells stained with A03146-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PMM2 Antibody (A03146-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-pancreatic-lipase-pnlip-picoband-trade-antibody-a04935-1-boster.html2026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04935-1-pnlip-primary-antibodies-wb-testing-1.jpgAnti-Pancreatic Lipase/PNLIP Antibody Picoband® Western blot analysis of Pancreatic Lipase/PNLIP using anti-Pancreatic Lipase/PNLIP antibody (A04935-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat pancreas tissue lysates, Lane 2: mouse pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Pancreatic Lipase/PNLIP antigen affinity purified polyclonal antibody (Catalog # A04935-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Pancreatic Lipase/PNLIP at approximately 51 kDa. The expected band size for Pancreatic Lipase/PNLIP is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04935-1-pnlip-primary-antibodies-if-testing-2.jpgAnti-Pancreatic Lipase/PNLIP Antibody Picoband® IF analysis of Pancreatic Lipase/PNLIP using anti-Pancreatic Lipase/PNLIP antibody (A04935-1). Pancreatic Lipase/PNLIP was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Pancreatic Lipase/PNLIP Antibody (A04935-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04935-1-pnlip-primary-antibodies-fcm-testing-3.pngAnti-Pancreatic Lipase/PNLIP Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-Pancreatic Lipase/PNLIP antibody (A04935-1). Overlay histogram showing U251 cells stained with A04935-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Pancreatic Lipase/PNLIP Antibody (A04935-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/primary-antibodies/anti-integrin-alpha-9-itga9-picoband-trade-antibody-a06851-1-boster.html2026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06851-1-itga9-primary-antibodies-wb-testing-1.jpgAnti-Integrin alpha-9/ITGA9 Antibody Picoband® Western blot analysis of Integrin Alpha-9/ITGA9 using anti-Integrin Alpha-9/ITGA9 antibody (A06851-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Integrin Alpha-9/ITGA9 antigen affinity purified polyclonal antibody (Catalog # A06851-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Integrin Alpha-9/ITGA9 at approximately 120 kDa. The expected band size for Integrin Alpha-9/ITGA9 is at 115 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06851-1-itga9-primary-antibodies-fcm-testing-2.pngAnti-Integrin alpha-9/ITGA9 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-Integrin Alpha-9/ITGA9 antibody (A06851-1). Overlay histogram showing SH-SY5Y cells stained with A06851-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Integrin Alpha-9/ITGA9 Antibody (A06851-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256282026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2269.jpgHuman NUDT5 ELISA Kit PicoKine®Human NUDT5 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256292026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2270.pngHuman OSCAR ELISA Kit PicoKine®Human OSCAR PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256302026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2271.jpgRat CD25/IL2RA ELISA Kit PicoKine®Rat CD25 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256312026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2272.jpgHuman Olfactomedin-2/Noelin-2 ELISA Kit PicoKine®Human Olfactomedin-2/Noelin-2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256322026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2273.pngHuman Nidogen2 ELISA Kit PicoKine®Human Nidogen2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256332026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2274.pngHuman MFAP5 ELISA Kit PicoKine®Human MFAP5 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256342026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2275.jpgHuman NOTCH3 ELISA Kit PicoKine®Human NOTCH3 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256352026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2276.pngHuman NPTXR ELISA Kit PicoKine®Human NPTXR PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256362026-03-10T04:37:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2277.pngHuman NQO1 ELISA Kit PicoKine®Human NQO1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1256382026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07690-1-pgm2-primary-antibodies-wb-testing-1.jpgAnti-PGM2 Antibody Picoband® Western blot analysis of PGM2 using anti-PGM2 antibody (A07690-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGM2 antigen affinity purified polyclonal antibody (Catalog # A07690-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGM2 at approximately 75 kDa. The expected band size for PGM2 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07690-1-pgm2-primary-antibodies-if-testing-2.jpgAnti-PGM2 Antibody Picoband® IF analysis of PGM2 using anti-PGM2 antibody (A07690-1). PGM2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PGM2 Antibody (A07690-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07690-1-pgm2-primary-antibodies-fcm-testing-3.pngAnti-PGM2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-PGM2 antibody (A07690-1). Overlay histogram showing HEL cells stained with A07690-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PGM2 Antibody (A07690-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256392026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16087-1-phf24-primary-antibodies-wb-testing-1.jpgAnti-PHF24 Antibody Picoband® Western blot analysis of PHF24 using anti-PHF24 antibody (A16087-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF24 antigen affinity purified polyclonal antibody (Catalog # A16087-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHF24 at approximately 45 kDa. The expected band size for PHF24 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16087-1-phf24-primary-antibodies-fcm-testing-2.pngAnti-PHF24 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PHF24 antibody (A16087-1). Overlay histogram showing SH-SY5Y cells stained with A16087-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHF24 Antibody (A16087-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256402026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00988-2-pnp-primary-antibodies-wb-testing-1.jpgAnti-PNP Antibody Picoband® Western blot analysis of PNP using anti-PNP antibody (A00988-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human U-937 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse ANA-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PNP antigen affinity purified polyclonal antibody (Catalog # A00988-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PNP at approximately 32 kDa. The expected band size for PNP is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00988-2-pnp-primary-antibodies-fcm-testing-2.pngAnti-PNP Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PNP antibody (A00988-2). Overlay histogram showing JK cells stained with A00988-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PNP Antibody (A00988-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256412026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09557-1-pnpla1-primary-antibodies-wb-testing-1.jpgAnti-PNPLA1 Antibody Picoband® Western blot analysis of PNPLA1 using anti-PNPLA1 antibody (A09557-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PNPLA1 antigen affinity purified polyclonal antibody (Catalog # A09557-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PNPLA1 at approximately 58 kDa. The expected band size for PNPLA1 is at 58 kDa. https://www.bosterbio.com/catalog/product/view/id/1256432026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12979-1-nt5m-primary-antibodies-wb-testing-1.jpgAnti-NT5M Antibody Picoband® Western blot analysis of NT5M using anti-NT5M antibody (A12979-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NT5M antigen affinity purified polyclonal antibody (Catalog # A12979-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NT5M at approximately 26 kDa. The expected band size for NT5M is at 26 kDa. https://www.bosterbio.com/catalog/product/view/id/1256442026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15642-perm1-primary-antibodies-wb-testing-1.jpgAnti-PERM1 Antibody Picoband® Western blot analysis of PERM1 using anti-PERM1 antibody (A15642). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PERM1 antigen affinity purified polyclonal antibody (Catalog # A15642) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PERM1 at approximately 75 kDa. The expected band size for PERM1 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15642-perm1-primary-antibodies-if-testing-2.jpgAnti-PERM1 Antibody Picoband® IF analysis of PERM1 using anti-PERM1 antibody (A15642) and anti-Beta Tubulin antibody (M01857-3). PERM1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PERM1 Antibody (A15642) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127)(B) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133)(D) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI(C). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15642-perm1-primary-antibodies-fcm-testing-3.pngAnti-PERM1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PERM1 antibody (A15642). Overlay histogram showing MCF-7 cells stained with A15642 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PERM1 Antibody (A15642, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256452026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06841-phpt1-primary-antibodies-wb-testing-1.jpgAnti-PHPT1 Antibody Picoband® Western blot analysis of PHPT1 using anti-PHPT1 antibody (A06841). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHPT1 antigen affinity purified polyclonal antibody (Catalog # A06841) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHPT1 at approximately 14 kDa. The expected band size for PHPT1 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06841-phpt1-primary-antibodies-ihc-testing-2.jpgAnti-PHPT1 Antibody Picoband® IHC analysis of PHPT1 using anti-PHPT1 antibody (A06841). PHPT1 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHPT1 Antibody (A06841) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06841-phpt1-primary-antibodies-ihc-testing-3.jpgAnti-PHPT1 Antibody Picoband® IHC analysis of PHPT1 using anti-PHPT1 antibody (A06841). PHPT1 was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHPT1 Antibody (A06841) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06841-phpt1-primary-antibodies-fcm-testing-4.pngAnti-PHPT1 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-PHPT1 antibody (A06841). Overlay histogram showing THP-1 cells stained with A06841 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHPT1 Antibody (A06841, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256462026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07451-1-pid1-primary-antibodies-wb-testing-1.jpgAnti-PID1 Antibody Picoband® Western blot analysis of PID1 using anti-PID1 antibody (A07451-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat brain tissue lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PID1 antigen affinity purified polyclonal antibody (Catalog # A07451-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PID1 at approximately 28 kDa. The expected band size for PID1 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07451-1-pid1-primary-antibodies-fcm-testing-2.pngAnti-PID1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-PID1 antibody (A07451-1). Overlay histogram showing U251 cells stained with A07451-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PID1 Antibody (A07451-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256472026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-wb-testing-1.jpgAnti-PITHD1 Antibody Picoband® Western blot analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat thymus tissue lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PITHD1 antigen affinity purified polyclonal antibody (Catalog # A15347-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PITHD1 at approximately 24 kDa. The expected band size for PITHD1 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-2.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human ganglioneuroma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-3.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human ganglioneuroma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-4.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-5.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-6.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-7.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-8.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human rectum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-9.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human rectum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-10.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-11.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-12.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-ihc-testing-13.jpgAnti-PITHD1 Antibody Picoband® IHC analysis of PITHD1 using anti-PITHD1 antibody (A15347-1). PITHD1 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PITHD1 Antibody (A15347-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-if-testing-14.jpgAnti-PITHD1 Antibody Picoband® IF analysis of PITHD1 using anti-PITHD1 antibody (A15347-1) and anti-Beta Tubulin antibody (M01857-3). PITHD1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PITHD1 Antibody (A15347-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15347-1-pithd-primary-antibodies-fcm-testing-15.pngAnti-PITHD1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-PITHD1 antibody (A15347-1). Overlay histogram showing HEL cells stained with A15347-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PITHD1 Antibody (A15347-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256482026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-wb-testing-1.jpgAnti-TNS3 Antibody Picoband® Western blot analysis of TNS3 using anti-TNS3 antibody (A07345-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNS3 antigen affinity purified polyclonal antibody (Catalog # A07345-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TNS3 at approximately 200 kDa. The expected band size for TNS3 is at 155 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-ihc-testing-2.jpgAnti-TNS3 Antibody Picoband® IHC analysis of TNS3 using anti-TNS3 antibody (A07345-1). TNS3 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNS3 Antibody (A07345-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-ihc-testing-3.jpgAnti-TNS3 Antibody Picoband® IHC analysis of TNS3 using anti-TNS3 antibody (A07345-1). TNS3 was detected in a paraffin-embedded section of human endometrioid adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNS3 Antibody (A07345-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-ihc-testing-4.jpgAnti-TNS3 Antibody Picoband® IHC analysis of TNS3 using anti-TNS3 antibody (A07345-1). TNS3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNS3 Antibody (A07345-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-ihc-testing-5.jpgAnti-TNS3 Antibody Picoband® IHC analysis of TNS3 using anti-TNS3 antibody (A07345-1). TNS3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNS3 Antibody (A07345-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-ihc-testing-6.jpgAnti-TNS3 Antibody Picoband® IHC analysis of TNS3 using anti-TNS3 antibody (A07345-1). TNS3 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNS3 Antibody (A07345-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-ihc-testing-7.jpgAnti-TNS3 Antibody Picoband® IHC analysis of TNS3 using anti-TNS3 antibody (A07345-1). TNS3 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TNS3 Antibody (A07345-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-if-testing-8.jpgAnti-TNS3 Antibody Picoband® IF analysis of TNS3 using anti-TNS3 antibody (A07345-1). TNS3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TNS3 Antibody (A07345-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-fcm-testing-9.pngAnti-TNS3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-TNS3 antibody (A07345-1). Overlay histogram showing U251 cells stained with A07345-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TNS3 Antibody (A07345-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07345-1-tns3-primary-antibodies-ip-testing-10.jpgAnti-TNS3 Antibody Picoband® Immunoprecipitating TNS3 in U251 whole cell lysate . Western blot analysis of TNS3 using anti-TNS3 antibody (A07345-1). Lane 1: U251 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-TNS3 antibody in U251 whole cell lysate, Lane 3: anti-TNS3 antibody (2μg) + U251 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TNS3 antigen affinity purified polyclonal antibody (A07345-1) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for TNS3 at approximately 200 kDa. The expected band size for TNS3 is at 155 kDa. https://www.bosterbio.com/catalog/product/view/id/1256492026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09089-1-tnrc6c-primary-antibodies-wb-testing-1.jpgAnti-TNRC6C Antibody Picoband® Western blot analysis of TNRC6C using anti-TNRC6C antibody (A09089-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TNRC6C antigen affinity purified polyclonal antibody (Catalog # A09089-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TNRC6C at approximately 210 kDa. The expected band size for TNRC6C is at 176 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09089-1-tnrc6c-primary-antibodies-if-testing-2.jpgAnti-TNRC6C Antibody Picoband® IF analysis of TNRC6C using anti-TNRC6C antibody (A09089-1) and anti-Beta Tubulin antibody (M01857-3). TNRC6C was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TNRC6C Antibody (A09089-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127)(B) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133)(D) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI(C). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09089-1-tnrc6c-primary-antibodies-fcm-testing-3.pngAnti-TNRC6C Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-TNRC6C antibody (A09089-1). Overlay histogram showing HEL cells stained with A09089-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TNRC6C Antibody (A09089-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256502026-03-17T05:15:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-wb-testing-1.jpgAnti-PLBD2 Antibody Picoband® Western blot analysis of PLBD2 using anti-PLBD2 antibody (A12971). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLBD2 antigen affinity purified polyclonal antibody (Catalog # A12971) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLBD2 at approximately 75 kDa. The expected band size for PLBD2 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-2.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-3.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-4.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human rectum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-5.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human rectum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-6.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-7.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-8.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-ihc-testing-9.jpgAnti-PLBD2 Antibody Picoband® IHC analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-if-testing-10.jpgAnti-PLBD2 Antibody Picoband® IF analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-fcm-testing-11.pngAnti-PLBD2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PLBD2 antibody (A12971). Overlay histogram showing HepG2 cells stained with A12971 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PLBD2 Antibody (A12971, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12971-plbd2-primary-antibodies-if-testing-12.jpgAnti-PLBD2 Antibody Picoband® IF analysis of PLBD2 using anti-PLBD2 antibody (A12971). PLBD2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PLBD2 Antibody (A12971) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256512026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10941-1-plxnc1-primary-antibodies-wb-testing-1.jpgAnti-PLXNC1 Antibody Picoband® Western blot analysis of PLXNC1 using anti-PLXNC1 antibody (A10941-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLXNC1 antigen affinity purified polyclonal antibody (Catalog # A10941-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLXNC1 at approximately 220 kDa. The expected band size for PLXNC1 is at 176 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10941-1-plxnc1-primary-antibodies-fcm-testing-2.pngAnti-PLXNC1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PLXNC1 antibody (A10941-1). Overlay histogram showing HepG2 cells stained with A10941-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PLXNC1 Antibody (A10941-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256522026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05782-2-mapre3-primary-antibodies-wb-testing-1_1.jpgAnti-EB3/MAPRE3 Antibody Picoband®Western blot analysis of EB3/MAPRE3 using anti-EB3/MAPRE3 antibody (A05782-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EB3/MAPRE3 antigen affinity purified polyclonal antibody (Catalog # A05782-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EB3/MAPRE3 at approximately 35 kDa. The expected band size for EB3/MAPRE3 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05782-2-mapre3-primary-antibodies-fcm-testing-1.jpgAnti-EB3/MAPRE3 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-EB3/MAPRE3 antibody (A05782-2). Overlay histogram showing 293T cells stained with A05782-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EB3/MAPRE3 Antibody (A05782-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1256532026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06022-mmd-primary-antibodies-wb-testing-1.jpgAnti-MMD Antibody Picoband® Western blot analysis of MMD using anti-MMD antibody (A06022). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MMD antigen affinity purified polyclonal antibody (Catalog # A06022) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MMD at approximately 28 kDa. The expected band size for MMD is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06022-fimmu-15-1422497-g006.jpgAnti-MMD Antibody Picoband®Differential expression and ROC curve of OFGs of ferroptosis. (A) The expression difference of ACO1 between TAO and Normal. (B) The expression difference of HCRA1 between TAO and Normal. (C) The expression difference of MMD between TAO and Normal. (D) The predictive value of ACO1 in TAO from the ROC curve. (E) The predictive value of HCRA1 in TAO from the ROC curve. (F) The predictive value of MMD in TAO from the ROC curve. Each panel displayed the AUC under the curve and 95% CI. ROC, ROC curve; AUC, area under the curve; CI, confidence interval. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1422497/full'>39735537</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06022-fimmu-15-1422497-g007.jpgAnti-MMD Antibody Picoband®GSEA analysis of OFGs for ferroptosis in TAO. (A) GSEA analysis of ACO1. (B) GSEA analysis of HCRA1. (C) GSEA analysis of MMD. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/immunology/articles/10.3389/fimmu.2024.1422497/full'>39735537</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06022-mmd-primary-antibodies-fcm-testing-2.pngAnti-MMD Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-MMD antibody (A06022). Overlay histogram showing SH-SY5Y cells stained with A06022 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MMD Antibody (A06022, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256542026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09516-2-mobp-primary-antibodies-wb-testing-1.jpgAnti-MOBP Antibody Picoband® Western blot analysis of MOBP using anti-MOBP antibody (A09516-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOBP antigen affinity purified polyclonal antibody (Catalog # A09516-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOBP at approximately 21 kDa. The expected band size for MOBP is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09516-2-mobp-primary-antibodies-fcm-testing-2.pngAnti-MOBP Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-MOBP antibody (A09516-2). Overlay histogram showing SH-SY5Y cells stained with A09516-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOBP Antibody (A09516-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256552026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03553-1-rnase1-primary-antibodies-wb-testing-1.jpgAnti-RNASE1 Antibody Picoband® Western blot analysis of RNASE1 using anti-RNASE1 antibody (A03553-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat pancreas tissue lysates, Lane 2: mouse pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RNASE1 antigen affinity purified polyclonal antibody (Catalog # A03553-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RNASE1 at approximately 18 kDa. The expected band size for RNASE1 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03553-1-rnase1-primary-antibodies-fcm-testing-2.pngAnti-RNASE1 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-RNASE1 antibody (A03553-1). Overlay histogram showing U20S cells stained with A03553-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RNASE1 Antibody (A03553-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256562026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00133-1-abl1-primary-antibodies-wb-testing-1.jpgAnti-ABL1 Antibody Picoband® Western blot analysis of ABL1 using anti-ABL1 antibody (A00133-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human MDA-MB-453 whole cell lysates, Lane 4: human Raji whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABL1 antigen affinity purified polyclonal antibody (Catalog # A00133-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ABL1 at approximately 143 kDa. The expected band size for ABL1 is at 133 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00133-1-abl1-primary-antibodies-if-testing-2.jpgAnti-ABL1 Antibody Picoband® IF analysis of ABL1 using anti-ABL1 antibody (A00133-1) and anti-Beta Tubulin antibody (M01857-3). ABL1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ABL1 Antibody (A00133-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00133-1-abl1-primary-antibodies-fcm-testing-3.pngAnti-ABL1 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-ABL1 antibody (A00133-1). Overlay histogram showing PC-3 cells stained with A00133-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABL1 Antibody (A00133-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00133-1-abl1-primary-antibodies-fcm-testing-4.pngAnti-ABL1 Antibody Picoband® Flow Cytometry analysis of PC-12 cells using anti-ABL1 antibody (A00133-1). Overlay histogram showing PC-12 cells stained with A00133-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABL1 Antibody (A00133-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00133-1-abl1-primary-antibodies-fcm-testing-5.pngAnti-ABL1 Antibody Picoband® Flow Cytometry analysis of RAW264.7 cells using anti-ABL1 antibody (A00133-1). Overlay histogram showing RAW264.7 cells stained with A00133-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABL1 Antibody (A00133-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256582026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01487-2-arhgef5-primary-antibodies-wb-testing-1.jpgAnti-ARHGEF5 Antibody Picoband® Western blot analysis of ARHGEF5 using anti-ARHGEF5 antibody (A01487-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARHGEF5 antigen affinity purified polyclonal antibody (Catalog # A01487-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARHGEF5 at approximately 250 kDa. The expected band size for ARHGEF5 is at 177 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01487-2-arhgef5-primary-antibodies-wb-testing-2.jpgAnti-ARHGEF5 Antibody Picoband® Western blot analysis of ARHGEF5 using anti-ARHGEF5 antibody (A01487-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat NRK whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARHGEF5 antigen affinity purified polyclonal antibody (Catalog # A01487-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARHGEF5 at approximately 250 kDa. The expected band size for ARHGEF5 is at 177 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01487-2-arhgef5-primary-antibodies-fcm-testing-3.pngAnti-ARHGEF5 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-ARHGEF5 antibody (A01487-2). Overlay histogram showing PC-3 cells stained with A01487-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARHGEF5 Antibody (A01487-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01487-2-arhgef5-primary-antibodies-fcm-testing-4.pngAnti-ARHGEF5 Antibody Picoband® Flow Cytometry analysis of PC-12 cells using anti-ARHGEF5 antibody (A01487-2). Overlay histogram showing PC-12 cells stained with A01487-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARHGEF5 Antibody (A01487-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01487-2-arhgef5-primary-antibodies-fcm-testing-5.pngAnti-ARHGEF5 Antibody Picoband® Flow Cytometry analysis of RAW264.7 cells using anti-ARHGEF5 antibody (A01487-2). Overlay histogram showing RAW264.7 cells stained with A01487-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARHGEF5 Antibody (A01487-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256602026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00756-3-ace2-primary-antibodies-wb-testing-1.jpgAnti-ACE2 Antibody Picoband® Western blot analysis of ACE2 using anti-ACE2 antibody (A00756-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACE2 antigen affinity purified polyclonal antibody (Catalog # A00756-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACE2 at approximately 120 kDa. The expected band size for ACE2 is at 93 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00756-3-ace2-primary-antibodies-fcm-testing-2.pngAnti-ACE2 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-ACE2 antibody (A00756-3). Overlay histogram showing SH-SY5Y cells stained with A00756-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ACE2 Antibody (A00756-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256612026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08872-1-bpifb1-primary-antibodies-wb-testing-1.jpgAnti-BPIFB1 Antibody Picoband® Western blot analysis of BPIFB1 using anti-BPIFB1 antibody (A08872-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BPIFB1 antigen affinity purified polyclonal antibody (Catalog # A08872-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BPIFB1 at approximately 52 kDa. The expected band size for BPIFB1 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08872-1-bpifb1-primary-antibodies-fcm-testing-2.pngAnti-BPIFB1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-BPIFB1 antibody (A08872-1). Overlay histogram showing HepG2 cells stained with A08872-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-BPIFB1 Antibody (A08872-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256632026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-wb-testing-1.jpgAnti-ASH2L Antibody Picoband® Western blot analysis of ASH2L using anti-ASH2L antibody (A06129-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ASH2L antigen affinity purified polyclonal antibody (Catalog # A06129-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ASH2L at approximately 69,80 kDa. The expected band size for ASH2L is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-2.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-3.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-4.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-5.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-6.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-7.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-8.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human rectum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-9.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human rectum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-10.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-11.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-12.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-13.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-14.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-15.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-16.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-17.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-18.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-ihc-testing-19.jpgAnti-ASH2L Antibody Picoband® IHC analysis of ASH2L using anti-ASH2L antibody (A06129-1). ASH2L was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASH2L Antibody (A06129-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-if-testing-20.jpgAnti-ASH2L Antibody Picoband® IF analysis of ASH2L using anti-ASH2L antibody (A06129-1) and anti-Beta Tubulin antibody (M01857-3). ASH2L was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ASH2L Antibody (A06129-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127)(B) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133)(D) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI(C). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06129-1-ash2l-primary-antibodies-fcm-testing-21.pngAnti-ASH2L Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-ASH2L antibody (A06129-1). Overlay histogram showing U20S cells stained with A06129-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ASH2L Antibody (A06129-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256642026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04553-1-cnepe-primary-antibodies-wb-testing-1.jpgAnti-Cenpe Antibody Picoband® Western blot analysis of Cenpe using anti-Cenpe antibody (A04553-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cenpe antigen affinity purified polyclonal antibody (Catalog # A04553-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cenpe at approximately 300 kDa. The expected band size for Cenpe is at 316 kDa. https://www.bosterbio.com/catalog/product/view/id/1256662026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04884-3-cnot7-primary-antibodies-wb-testing-1.jpgAnti-CNOT7 Antibody Picoband® Western blot analysis of CNOT7 using anti-CNOT7 antibody (A04884-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human MOLT-4 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CNOT7 antigen affinity purified polyclonal antibody (Catalog # A04884-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CNOT7 at approximately 33 kDa. The expected band size for CNOT7 is at 33 kDa. https://www.bosterbio.com/catalog/product/view/id/1256672026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-wb-testing-1.jpgAnti-ARHGEF7 Antibody Picoband® Western blot analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse skeletal muscle lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARHGEF7 antigen affinity purified polyclonal antibody (Catalog # A02764-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARHGEF7 at approximately 80 kDa. The expected band size for ARHGEF7 is at 90 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-2.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-3.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-4.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-5.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-6.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-7.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-8.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-9.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-10.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-ihc-testing-11.jpgAnti-ARHGEF7 Antibody Picoband® IHC analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-if-testing-12.jpgAnti-ARHGEF7 Antibody Picoband® IF analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-fcm-testing-13.pngAnti-ARHGEF7 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-ARHGEF7 antibody (A02764-2). Overlay histogram showing THP-1 cells stained with A02764-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARHGEF7 Antibody (A02764-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-if-testing-14.jpgAnti-ARHGEF7 Antibody Picoband® IF analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02764-2-arhgef7-primary-antibodies-if-testing-15.jpgAnti-ARHGEF7 Antibody Picoband® IF analysis of ARHGEF7 using anti-ARHGEF7 antibody (A02764-2). ARHGEF7 was detected in a paraffin-embedded section of human prostste cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ARHGEF7 Antibody (A02764-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256682026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02855-2-xrn1-primary-antibodies-wb-testing-1.jpgAnti-XRN1 Antibody Picoband® Western blot analysis of XRN1 using anti-XRN1 antibody (A02855-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-XRN1 antigen affinity purified polyclonal antibody (Catalog # A02855-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for XRN1 at approximately 200 kDa. The expected band size for XRN1 is at 194 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02855-2-xrn1-primary-antibodies-if-testing-2.jpgAnti-XRN1 Antibody Picoband® IF analysis of XRN1 using anti-XRN1 antibody (A02855-2). XRN1 was detected in an immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-XRN1 Antibody (A02855-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256692026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06073-2-atp6v1b1-primary-antibodies-wb-testing-1.jpgAnti-ATP6V1B1 Antibody Picoband® Western blot analysis of ATP6V1B1 using anti-ATP6V1B1 antibody (A06073-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP6V1B1 antigen affinity purified polyclonal antibody (Catalog # A06073-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP6V1B1 at approximately 69 kDa. The expected band size for ATP6V1B1 is at 57 kDa. https://www.bosterbio.com/catalog/product/view/id/1256702026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01586-3-ncf1-primary-antibodies-wb-testing-1.jpgAnti-p47 phox/NCF1 Antibody Picoband® Western blot analysis of P47 Phox/NCF1 using anti-P47 Phox/NCF1 antibody (A01586-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human Ramos whole cell lysates, Lane 4: rat spleen tissue lysates, Lane 5: mouse thymus tissue lysates, Lane 6: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P47 Phox/NCF1 antigen affinity purified polyclonal antibody (Catalog # A01586-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for P47 Phox/NCF1 at approximately 40-50 kDa. The expected band size for P47 Phox/NCF1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01586-3-ncf1-primary-antibodies-ihc-testing-2.jpgAnti-p47 phox/NCF1 Antibody Picoband® IHC analysis of P47 Phox/NCF1 using anti-P47 Phox/NCF1 antibody (A01586-3). P47 Phox/NCF1 was detected in a paraffin-embedded section of rat lymph tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-P47 Phox/NCF1 Antibody (A01586-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01586-3-ncf1-primary-antibodies-ihc-testing-3.jpgAnti-p47 phox/NCF1 Antibody Picoband® IHC analysis of P47 Phox/NCF1 using anti-P47 Phox/NCF1 antibody (A01586-3). P47 Phox/NCF1 was detected in a paraffin-embedded section of mouse lymph tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-P47 Phox/NCF1 Antibody (A01586-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01586-3-ncf1-primary-antibodies-fcm-testing-4.pngAnti-p47 phox/NCF1 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-P47 Phox/NCF1 antibody (A01586-3). Overlay histogram showing THP-1 cells stained with A01586-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-P47 Phox/NCF1 Antibody (A01586-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01586-3-ncf1-primary-antibodies-if-testing-5.jpgAnti-p47 phox/NCF1 Antibody Picoband® IF analysis of Phox/NCF1 using anti-Phox/NCF1 antibody (A01586-3). Phox/NCF1 was detected in a paraffin-embedded section of mouse lymph node tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Phox/NCF1 Antibody (A01586-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01586-3-ncf1-primary-antibodies-if-testing-6.jpgAnti-p47 phox/NCF1 Antibody Picoband® IF analysis of Phox/NCF1 using anti-Phox/NCF1 antibody (A01586-3). Phox/NCF1 was detected in a paraffin-embedded section of rat lymph node tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-Phox/NCF1 Antibody (A01586-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256712026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08350-1-capn5-primary-antibodies-wb-testing-1.jpgAnti-CAPN5 Antibody Picoband® Western blot analysis of CAPN5 using anti-CAPN5 antibody (A08350-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CAPN5 antigen affinity purified polyclonal antibody (Catalog # A08350-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CAPN5 at approximately 73 kDa. The expected band size for CAPN5 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08350-1-capn5-primary-antibodies-if-testing-2.jpgAnti-CAPN5 Antibody Picoband® IF analysis of CAPN5 using anti-CAPN5 antibody (A08350-1). CAPN5 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CAPN5 Antibody (A08350-1) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08350-1-capn5-primary-antibodies-fcm-testing-3.pngAnti-CAPN5 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-CAPN5 antibody (A08350-1). Overlay histogram showing U251 cells stained with A08350-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CAPN5 Antibody (A08350-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256722026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01994-2-at1l-primary-antibodies-wb-testing-1_1.jpgAnti-ATL1 Antibody Picoband®Western blot analysis of ATL1 using anti-ATL1 antibody (A01994-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATL1 antigen affinity purified polyclonal antibody (Catalog # A01994-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATL1 at approximately 64 kDa. The expected band size for ATL1 is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01994-2-at1l-primary-antibodies-if-testing-2.jpgAnti-ATL1 Antibody Picoband® IF analysis of ATL1 using anti-ATL1 antibody (A01994-2). ATL1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ATL1 Antibody (A01994-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01994-2-at1l-primary-antibodies-fcm-testing-3.pngAnti-ATL1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-ATL1 antibody (A01994-2). Overlay histogram showing SH-SY5Y cells stained with A01994-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ATL1 Antibody (A01994-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256732026-03-17T05:15:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-wb-testing-1.jpgAnti-LARG/ARHGEF12 Antibody Picoband® Western blot analysis of LARG/ARHGEF12 using anti-LARG/ARHGEF12 antibody (A06802-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LARG/ARHGEF12 antigen affinity purified polyclonal antibody (Catalog # A06802-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LARG/ARHGEF12 at approximately 220 kDa. The expected band size for LARG/ARHGEF12 is at 173 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-ihc-testing-2.jpgAnti-LARG/ARHGEF12 Antibody Picoband® IHC analysis of ARHGEF12L using anti-ARHGEF12L antibody (A06802-3). ARHGEF12L was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF12L Antibody (A06802-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-ihc-testing-3.jpgAnti-LARG/ARHGEF12 Antibody Picoband® IHC analysis of ARHGEF12L using anti-ARHGEF12L antibody (A06802-3). ARHGEF12L was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF12L Antibody (A06802-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-ihc-testing-4.jpgAnti-LARG/ARHGEF12 Antibody Picoband® IHC analysis of ARHGEF12L using anti-ARHGEF12L antibody (A06802-3). ARHGEF12L was detected in a paraffin-embedded section of human parotid acinar cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF12L Antibody (A06802-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-ihc-testing-5.jpgAnti-LARG/ARHGEF12 Antibody Picoband® IHC analysis of ARHGEF12L using anti-ARHGEF12L antibody (A06802-3). ARHGEF12L was detected in a paraffin-embedded section of human squamous cell carcinoma of cervix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF12L Antibody (A06802-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-ihc-testing-6.jpgAnti-LARG/ARHGEF12 Antibody Picoband® IHC analysis of ARHGEF12L using anti-ARHGEF12L antibody (A06802-3). ARHGEF12L was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARHGEF12L Antibody (A06802-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-if-testing-7.jpgAnti-LARG/ARHGEF12 Antibody Picoband® IF analysis of ARHGEF12 using anti-ARHGEF12 antibody (A06802-3) and anti-Beta Tubulin antibody (M01857-3). ARHGEF12 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ARHGEF12 Antibody (A06802-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-fcm-testing-8.pngAnti-LARG/ARHGEF12 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-LARG/ARHGEF12 antibody (A06802-3). Overlay histogram showing HepG2 cells stained with A06802-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LARG/ARHGEF12 Antibody (A06802-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06802-3-arhgef12-primary-antibodies-ip-testing-9.jpgAnti-LARG/ARHGEF12 Antibody Picoband® Immunoprecipitating (IP) LARG/ARHGEF12 in HepG2 whole cell lysate. Western blot analysis of LARG/ARHGEF12 using anti-LARG/ARHGEF12 antibody (A06802-3); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-LARG/ARHGEF12 antibody in HepG2 whole cell lysate; Lane 3: anti-LARG/ARHGEF12 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-LARG/ARHGEF12 antigen affinity purified polyclonal antibody (A06802-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for LARG/ARHGEF12 at approximately 220 kDa. The expected band size for LARG/ARHGEF12 is at 173 kDa. https://www.bosterbio.com/catalog/product/view/id/1256742026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-wb-testing-1.jpgAnti-ME3 Antibody Picoband® Western blot analysis of ME3 using anti-ME3 antibody (A05164-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: monkey COS7 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat heart tissue lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse kidney tissue lysates, Lane 8: mouse heart tissue lysates, Lane 9: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ME3 antigen affinity purified polyclonal antibody (Catalog # A05164-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ME3 at approximately 67 kDa. The expected band size for ME3 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-2.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-3.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-4.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-5.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-6.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-7.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-8.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-9.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-10.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-ihc-testing-11.jpgAnti-ME3 Antibody Picoband® IHC analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-fcm-testing-12.pngAnti-ME3 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-ME3 antibody (A05164-2). Overlay histogram showing HEL cells stained with A05164-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ME3 Antibody (A05164-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-if-testing-13.jpgAnti-ME3 Antibody Picoband® IF analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-if-testing-14.jpgAnti-ME3 Antibody Picoband® IF analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05164-2-me3-primary-antibodies-if-testing-15.jpgAnti-ME3 Antibody Picoband® IF analysis of ME3 using anti-ME3 antibody (A05164-2). ME3 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ME3 Antibody (A05164-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256752026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04862-1-syngap1-primary-antibodies-wb-testing-1.jpgAnti-SYNGAP1 Antibody Picoband® Western blot analysis of SYNGAP1 using anti-SYNGAP1 antibody (A04862-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SYNGAP1 antigen affinity purified polyclonal antibody (Catalog # A04862-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SYNGAP1 at approximately 148 kDa. The expected band size for SYNGAP1 is at 148 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04862-1-syngap1-primary-antibodies-fcm-testing-2.pngAnti-SYNGAP1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-SYNGAP1 antibody (A04862-1). Overlay histogram showing K562 cells stained with A04862-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SYNGAP1 Antibody (A04862-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256762026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02278-1-atp1a3-primary-antibodies-wb-testing-1.jpgAnti-ATP1A3 Antibody Picoband® Western blot analysis of ATP1A3 using anti-ATP1A3 antibody (A02278-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP1A3 antigen affinity purified polyclonal antibody (Catalog # A02278-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP1A3 at approximately 90 kDa. The expected band size for ATP1A3 is at 112 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02278-1-atp1a3-primary-antibodies-ihc-testing-1.jpgAnti-ATP1A3 Antibody Picoband®IHC analysis of ATP1A3 using anti-ATP1A3 antibody (A02278-1). ATP1A3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A3 Antibody (A02278-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02278-1-atp1a3-primary-antibodies-ihc-testing-2.jpgAnti-ATP1A3 Antibody Picoband®IHC analysis of ATP1A3 using anti-ATP1A3 antibody (A02278-1). ATP1A3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A3 Antibody (A02278-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02278-1-atp1a3-primary-antibodies-ihc-testing-3_1.jpgAnti-ATP1A3 Antibody Picoband®IHC analysis of ATP1A3 using anti-ATP1A3 antibody (A02278-1). ATP1A3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A3 Antibody (A02278-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1256782026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02360-1-plce1-primary-antibodies-wb-testing-1.jpgAnti-PLCE1 Antibody Picoband® Western blot analysis of PLCE1 using anti-PLCE1 antibody (A02360-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLCE1 antigen affinity purified polyclonal antibody (Catalog # A02360-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLCE1 at approximately 290 kDa. The expected band size for PLCE1 is at 259 kDa. https://www.bosterbio.com/catalog/product/view/id/1256792026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08678-1-yaf2-primary-antibodies-wb-testing-1.jpgAnti-YAF2 Antibody Picoband® Western blot analysis of YAF2 using anti-YAF2 antibody (A08678-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YAF2 antigen affinity purified polyclonal antibody (Catalog # A08678-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for YAF2 at approximately 25 kDa. The expected band size for YAF2 is at 20 kDa. https://www.bosterbio.com/catalog/product/view/id/1256802026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-2-tas2r10-primary-antibodies-wb-testing-1.jpgAnti-TAS2R10 Antibody Picoband® Western blot analysis of TAS2R10 using anti-TAS2R10 antibody (A10959-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TAS2R10 antigen affinity purified polyclonal antibody (Catalog # A10959-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TAS2R10 at approximately 38 kDa. The expected band size for TAS2R10 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-2-tas2r10-primary-antibodies-ihc-testing-2.jpgAnti-TAS2R10 Antibody Picoband® IHC analysis of TAS2R10 using anti-TAS2R10 antibody (A10959-2). TAS2R10 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TAS2R10 Antibody (A10959-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-2-tas2r10-primary-antibodies-ihc-testing-3.jpgAnti-TAS2R10 Antibody Picoband® IHC analysis of TAS2R10 using anti-TAS2R10 antibody (A10959-2). TAS2R10 was detected in a paraffin-embedded section of human cervix squamous cell carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TAS2R10 Antibody (A10959-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-2-tas2r10-primary-antibodies-fcm-testing-4.pngAnti-TAS2R10 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-TAS2R10 antibody (A10959-2). Overlay histogram showing HEL cells stained with A10959-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TAS2R10 Antibody (A10959-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10959-2-tas2r10-primary-antibodies-if-testing-5.jpgAnti-TAS2R10 Antibody Picoband® IF analysis of TAS2R10 using anti-TAS2R10 antibody (A10959-2). TAS2R10 was detected in a paraffin-embedded section of human cervix cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TAS2R10 Antibody (A10959-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256812026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04405-2-cd3d-primary-antibodies-wb-testing-1.jpgAnti-CD3D Antibody Picoband® Western blot analysis of CD3D using anti-CD3D antibody (A04405-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human CCRF-CEM whole cell lysates, Lane 3: human MOLT-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD3D antigen affinity purified polyclonal antibody (Catalog # A04405-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD3D at approximately 19 kDa. The expected band size for CD3D is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04405-2-cd3d-primary-antibodies-fcm-testing-2.pngAnti-CD3D Antibody Picoband® Flow Cytometry analysis of JK cells using anti-CD3D antibody (A04405-2). Overlay histogram showing JK cells stained with A04405-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD3D Antibody (A04405-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256822026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-2-cd44-primary-antibodies-wb-testing-1.jpgAnti-CD44 Antibody Picoband® Western blot analysis of CD44 using anti-CD44 antibody (A00052-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PANC-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD44 antigen affinity purified polyclonal antibody (Catalog # A00052-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD44 at approximately 85 kDa. The expected band size for CD44 is at 82 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-2-cd44-primary-antibodies-ihc-testing-2.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052-2). CD44 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD44 Antibody (A00052-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-2-cd44-primary-antibodies-ihc-testing-3.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052-2). CD44 was detected in a paraffin-embedded section of mouse lymphaden tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD44 Antibody (A00052-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-2-cd44-primary-antibodies-ihc-testing-4.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052-2). CD44 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD44 Antibody (A00052-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-2-cd44-primary-antibodies-ihc-testing-5.jpgAnti-CD44 Antibody Picoband® IHC analysis of CD44 using anti-CD44 antibody (A00052-2). CD44 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CD44 Antibody (A00052-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-2-cd44-primary-antibodies-if-testing-6.jpgAnti-CD44 Antibody Picoband® IF analysis of CD44 using anti-CD44 antibody (A00052-2). CD44 was detected in an immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CD44 Antibody (A00052-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00052-2-cd44-primary-antibodies-fcm-testing-7.pngAnti-CD44 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-CD44 antibody (A00052-2). Overlay histogram showing MCF-7 cells stained with A00052-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CD44 Antibody (A00052-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256832026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00006-4-pten-primary-antibodies-wb-testing-1.jpgAnti-PTEN Antibody Picoband® Western blot analysis of PTEN using anti-PTEN antibody (A00006-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: monkey COS-7 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat thymus tissue lysates, Lane 6: mouse thymus tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTEN antigen affinity purified polyclonal antibody (Catalog # A00006-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTEN at approximately 47 kDa. The expected band size for PTEN is at 47 kDa. https://www.bosterbio.com/catalog/product/view/id/1256852026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02747-1-cxadr-primary-antibodies-wb-testing-1.jpgAnti-CXADR Antibody Picoband® Western blot analysis of CXADR using anti-CXADR antibody (A02747-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CXADR antigen affinity purified polyclonal antibody (Catalog # A02747-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CXADR at approximately 45 kDa. The expected band size for CXADR is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02747-1-cxadr-primary-antibodies-if-testing-2.jpgAnti-CXADR Antibody Picoband® IF analysis of CXADR using anti-CXADR antibody (A02747-1). CXADR was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CXADR Antibody (A02747-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02747-1-cxadr-primary-antibodies-fcm-testing-3.pngAnti-CXADR Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-CXADR antibody (A02747-1). Overlay histogram showing HepG2 cells stained with A02747-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CXADR Antibody (A02747-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256872026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01061-4-sirt3-primary-antibodies-wb-testing-1.jpgAnti-SIRT3 Antibody Picoband® Western blot analysis of SIRT3 using anti-SIRT3 antibody (A01061-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIRT3 antigen affinity purified polyclonal antibody (Catalog # A01061-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SIRT3 at approximately 28 kDa. The expected band size for SIRT3 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01061-4-sirt3-primary-antibodies-wb-testing-2.jpgAnti-SIRT3 Antibody Picoband® Western blot analysis of SIRT3 using anti-SIRT3 antibody (A01061-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse liver tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIRT3 antigen affinity purified polyclonal antibody (Catalog # A01061-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SIRT3 at approximately 28 kDa. The expected band size for SIRT3 is at 44 kDa. https://www.bosterbio.com/catalog/product/view/id/1256882026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08729-2-tas1r2-primary-antibodies-wb-testing-1.jpgAnti-TAS1R2 Antibody Picoband® Western blot analysis of TAS1R2 using anti-TAS1R2 antibody (A08729-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PANC-1 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human COLO 320 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TAS1R2 antigen affinity purified polyclonal antibody (Catalog # A08729-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TAS1R2 at approximately 100 kDa. The expected band size for TAS1R2 is at 95 kDa. https://www.bosterbio.com/catalog/product/view/id/1256902026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-wb-testing-1.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® Western blot analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse testis tissue lysates, Lane 2: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-E-Cadherin/Cdh1 antigen affinity purified polyclonal antibody (Catalog # A00063-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for E-Cadherin/Cdh1 at approximately 120-130 kDa. The expected band size for E-Cadherin/Cdh1 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-ihc-testing-2.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® IHC analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). E-Cadherin/Cdh1 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-ihc-testing-3.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® IHC analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). E-Cadherin/Cdh1 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-ihc-testing-4.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® IHC analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). E-Cadherin/Cdh1 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-ihc-testing-5.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® IHC analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). E-Cadherin/Cdh1 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-fcm-testing-6.pngAnti-E-cadherin/Cdh1 Antibody Picoband® Flow Cytometry analysis of NIH/3T3 cells using anti-E-Cadherin/Cdh1 antibody (A00063-3). Overlay histogram showing NIH/3T3 cells stained with A00063-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-if-testing-7.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® IF analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). E-Cadherin/Cdh1 was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-if-testing-8.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® IF analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). E-Cadherin/Cdh1 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00063-3-cdh1-primary-antibodies-if-testing-9.jpgAnti-E-cadherin/Cdh1 Antibody Picoband® IF analysis of E-Cadherin/Cdh1 using anti-E-Cadherin/Cdh1 antibody (A00063-3). E-Cadherin/Cdh1 was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-E-Cadherin/Cdh1 Antibody (A00063-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256922026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-wb-testing-1.jpgAnti-MECP2 Antibody Picoband® Western blot analysis of MECP2 using anti-MECP2 antibody (A00047-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MDA-MB-453 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MECP2 antigen affinity purified polyclonal antibody (Catalog # A00047-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MECP2 at approximately 80 kDa. The expected band size for MECP2 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-ihc-testing-1.jpgAnti-MECP2 Antibody Picoband®IHC analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-ihc-testing-2.jpgAnti-MECP2 Antibody Picoband® IHC analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-ihc-testing-3.jpgAnti-MECP2 Antibody Picoband® IHC analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-ihc-testing-4.jpgAnti-MECP2 Antibody Picoband® IHC analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-ihc-testing-5.jpgAnti-MECP2 Antibody Picoband® IHC analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-ihc-testing-6.jpgAnti-MECP2 Antibody Picoband®IHC analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-if-testing-1.jpgAnti-MECP2 Antibody Picoband®IF analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00047-1-mecp2-primary-antibodies-if-testing-2.jpgAnti-MECP2 Antibody Picoband®IF analysis of MECP2 using anti-MECP2 antibody (A00047-1). MECP2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MECP2 Antibody (A00047-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1256942026-03-17T05:15:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00564-3-fn1-primary-antibodies-wb-testing-1.jpgAnti-Fibronectin/FN1 Antibody Picoband® Western blot analysis of Fibronectin/FN1 using anti-Fibronectin/FN1 antibody (A00564-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Fibronectin/FN1 antigen affinity purified polyclonal antibody (Catalog # A00564-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Fibronectin/FN1 at approximately 272 kDa. The expected band size for Fibronectin/FN1 is at 272 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00564-3-fn1-primary-antibodies-fcm-testing-2.pngAnti-Fibronectin/FN1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Fibronectin/FN1 antibody (A00564-3). Overlay histogram showing HepG2 cells stained with A00564-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Fibronectin/FN1 Antibody (A00564-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256952026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02411-1-cdcp1-primary-antibodies-wb-testing-1.jpgAnti-CDCP1 Antibody Picoband® Western blot analysis of CDCP1 using anti-CDCP1 antibody (A02411-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDCP1 antigen affinity purified polyclonal antibody (Catalog # A02411-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDCP1 at approximately 130 kDa. The expected band size for CDCP1 is at 93 kDa. https://www.bosterbio.com/catalog/product/view/id/1256972026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15311-1-pogk-primary-antibodies-wb-testing-1.jpgAnti-POGK Antibody Picoband® Western blot analysis of POGK using anti-POGK antibody (A15311-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POGK antigen affinity purified polyclonal antibody (Catalog # A15311-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POGK at approximately 95 kDa. The expected band size for POGK is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15311-1-pogk-primary-antibodies-if-testing-2.jpgAnti-POGK Antibody Picoband® IF analysis of POGK using anti-POGK antibody (A15311-1) and anti-Beta Tubulin antibody (M01857-3). POGK was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POGK Antibody (A15311-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15311-1-pogk-primary-antibodies-fcm-testing-3.pngAnti-POGK Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-POGK antibody (A15311-1). Overlay histogram showing SH-SY5Y cells stained with A15311-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POGK Antibody (A15311-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256982026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06169-3-pogz-primary-antibodies-wb-testing-1.jpgAnti-POGZ Antibody Picoband® Western blot analysis of POGZ using anti-POGZ antibody (A06169-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POGZ antigen affinity purified polyclonal antibody (Catalog # A06169-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POGZ at approximately 220 kDa. The expected band size for POGZ is at 155 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06169-3-pogz-primary-antibodies-if-testing-2.jpgAnti-POGZ Antibody Picoband® IF analysis of POGZ using anti-POGZ antibody (A06169-3) and anti-Beta Tubulin antibody (M01857-3). POGZ was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POGZ Antibody (A06169-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127)(B) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133)(D) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI(C). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06169-3-pogz-primary-antibodies-fcm-testing-3.pngAnti-POGZ Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-POGZ antibody (A06169-3). Overlay histogram showing HepG2 cells stained with A06169-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POGZ Antibody (A06169-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06169-3-pogz-primary-antibodies-fcm-testing-4.pngAnti-POGZ Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-POGZ antibody (A06169-3). Overlay histogram showing MCF-7 cells stained with A06169-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POGZ Antibody (A06169-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1256992026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05111-2-pold3-primary-antibodies-wb-testing-1.jpgAnti-POLD3 Antibody Picoband® Western blot analysis of POLD3 using anti-POLD3 antibody (A05111-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLD3 antigen affinity purified polyclonal antibody (Catalog # A05111-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLD3 at approximately 70 kDa. The expected band size for POLD3 is at 51 kDa. https://www.bosterbio.com/catalog/product/view/id/1257002026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09581-4-poldip2-primary-antibodies-wb-testing-1.jpgAnti-POLDIP2 Antibody Picoband® Western blot analysis of POLDIP2 using anti-POLDIP2 antibody (A09581-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLDIP2 antigen affinity purified polyclonal antibody (Catalog # A09581-4) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLDIP2 at approximately 36 kDa. The expected band size for POLDIP2 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09581-4-poldip2-primary-antibodies-ip-testing-4.jpgAnti-POLDIP2 Antibody Picoband® Immunoprecipitating POLDIP2 in HepG2 whole cell lysate. Western blot analysis of POLDIP2 using anti-POLDIP2 antibody (A09581-4); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-POLDIP2 antibody in HepG2 whole cell lysate; Lane 3: anti-POLDIP2 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-POLDIP2 antigen affinity purified polyclonal antibody (A09581-4) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for POLDIP2 at approximately 38 kDa. The expected band size for POLDIP2 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09581-4-poldip2-primary-antibodies-if-testing-2.jpgAnti-POLDIP2 Antibody Picoband® IF analysis of POLDIP2 using anti-POLDIP2 antibody (A09581-4). POLDIP2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POLDIP2 Antibody (A09581-4) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09581-4-poldip2-primary-antibodies-if-testing-1.jpgAnti-POLDIP2 Antibody Picoband®IF analysis of POLDIP2 using anti-POLDIP2 antibody (A09581-4). POLDIP2 was detected in an immunocytochemical section of human SK-HEP-1 cells. Cells were permeabilized with Triton X-100 (AR0205) for 10 minutes. The cells were blocked with 10% goat serum. And then incubated with 10 μg/mL rabbit anti-POLDIP2 Antibody (A09581-4) overnight at 4°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127), Cy3 conjugated goat anti-mouse IgG (BA1031) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09581-4-poldip2-primary-antibodies-fcm-testing-3.pngAnti-POLDIP2 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-POLDIP2 antibody (A09581-4). Overlay histogram showing U251 cells stained with A09581-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POLDIP2 Antibody (A09581-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257012026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09182-2-pole2-primary-antibodies-wb-testing-1.jpgAnti-POLE2 Antibody Picoband® Western blot analysis of POLE2 using anti-POLE2 antibody (A09182-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLE2 antigen affinity purified polyclonal antibody (Catalog # A09182-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLE2 at approximately 65 kDa. The expected band size for POLE2 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09182-2-pole2-primary-antibodies-fcm-testing-2.pngAnti-POLE2 Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-POLE2 antibody (A09182-2). Overlay histogram showing U20S cells stained with A09182-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POLE2 Antibody (A09182-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257022026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12720-1-polr3f-primary-antibodies-wb-testing-1.jpgAnti-POLR3F Antibody Picoband® Western blot analysis of POLR3F using anti-POLR3F antibody (A12720-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLR3F antigen affinity purified polyclonal antibody (Catalog # A12720-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLR3F at approximately 36 kDa. The expected band size for POLR3F is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12720-1-polr3f-primary-antibodies-if-testing-2.jpgAnti-POLR3F Antibody Picoband® IF analysis of POLR3F using anti-POLR3F antibody (A12720-1) and anti-Beta Tubulin antibody (M01857-3). POLR3F was detected in immunocytochemical section of MCF-7 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POLR3F Antibody (A12720-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127)(B) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133)(D) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI(C). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12720-1-polr3f-primary-antibodies-fcm-testing-3.pngAnti-POLR3F Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-POLR3F antibody (A12720-1). Overlay histogram showing A431 cells stained with A12720-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POLR3F Antibody (A12720-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257032026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03489-1-pomgnt1-primary-antibodies-wb-testing-1.jpgAnti-POMGNT1 Antibody Picoband® Western blot analysis of POMGNT1 using anti-POMGNT1 antibody (A03489-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POMGNT1 antigen affinity purified polyclonal antibody (Catalog # A03489-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POMGNT1 at approximately 75 kDa. The expected band size for POMGNT1 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03489-1-pomgnt1-primary-antibodies-ihc-testing-4.jpgAnti-POMGNT1 Antibody Picoband®IHC analysis of POMGNT1 using anti-POMGNT1 antibody (A03489-1). POMGNT1 was detected in a paraffin-embedded section of human heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POMGNT1 Antibody (A03489-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03489-1-pomgnt1-primary-antibodies-ihc-testing-2.jpgAnti-POMGNT1 Antibody Picoband® IHC analysis of POMGNT1 using anti-POMGNT1 antibody (A03489-1). POMGNT1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POMGNT1 Antibody (A03489-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03489-1-pomgnt1-primary-antibodies-ihc-testing-3.jpgAnti-POMGNT1 Antibody Picoband® IHC analysis of POMGNT1 using anti-POMGNT1 antibody (A03489-1). POMGNT1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POMGNT1 Antibody (A03489-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03489-1-pomgnt1-primary-antibodies-fcm-testing-4.pngAnti-POMGNT1 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-POMGNT1 antibody (A03489-1). Overlay histogram showing PC-3 cells stained with A03489-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POMGNT1 Antibody (A03489-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257042026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01291-2-cnr1-primary-antibodies-wb-testing-1.jpgAnti-Cannabinoid receptor 1/CNR1 Antibody Picoband® Western blot analysis of Cannabinoid Receptor 1/CNR1 using anti-Cannabinoid Receptor 1/CNR1 antibody (A01291-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cannabinoid Receptor 1/CNR1 antigen affinity purified polyclonal antibody (Catalog # A01291-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cannabinoid Receptor 1/CNR1 at approximately 53 kDa. The expected band size for Cannabinoid Receptor 1/CNR1 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01291-2-cnr1-primary-antibodies-fcm-testing-2.pngAnti-Cannabinoid receptor 1/CNR1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-Cannabinoid Receptor 1/CNR1 antibody (A01291-2). Overlay histogram showing U251 cells stained with A01291-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cannabinoid Receptor 1/CNR1 Antibody (A01291-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257052026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-wb-testing-1.jpgAnti-ATP4B Antibody Picoband® Western blot analysis of ATP4B using anti-ATP4B antibody (A08719-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat stomach tissue lysates, Lane 2: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP4B antigen affinity purified polyclonal antibody (Catalog # A08719-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP4B at approximately 75 kDa. The expected band size for ATP4B is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-wb-testing-2.pngAnti-ATP4B Antibody Picoband® Western blot analysis of ATP4B using anti-ATP4B antibody (A08719-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1:Normal group-rat colon tissue lysates, Lane 2:Model group-rat colon tissue lysates, Lane 3:Traditional Chinese medicine treatment (low concentration)-rat colon tissue lysates, Lane 4:Traditional Chinese medicine treatment (medium concentration)-rat colon tissue lysates, Lane 5:Traditional Chinese medicine treatment (High concentration)-rat colon tissue lysates, Lane 6:Western medicine treatment-rat colon tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP4B antigen affinity purified polyclonal antibody (Catalog # A08719-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with ChemiDoc MP system. A specific band was detected for ATP4B at approximately 70 kDa. The expected band size for ATP4B is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-ihc-testing-1.jpgAnti-ATP4B Antibody Picoband®IHC analysis of ATP4B using anti-ATP4B antibody (A08719-2). ATP4B was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP4B Antibody (A08719-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-ihc-testing-2.jpgAnti-ATP4B Antibody Picoband® IHC analysis of ATP4B using anti-ATP4B antibody (A08719-2). ATP4B was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP4B Antibody (A08719-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-ihc-testing-3.jpgAnti-ATP4B Antibody Picoband® IHC analysis of ATP4B using anti-ATP4B antibody (A08719-2). ATP4B was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP4B Antibody (A08719-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-ihc-testing-4.jpgAnti-ATP4B Antibody Picoband® IHC analysis of ATP4B using anti-ATP4B antibody (A08719-2). ATP4B was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP4B Antibody (A08719-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-ihc-testing-5.jpgAnti-ATP4B Antibody Picoband® IHC analysis of ATP4B using anti-ATP4B antibody (A08719-2). ATP4B was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP4B Antibody (A08719-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-fcm-testing-6.pngAnti-ATP4B Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ATP4B antibody (A08719-2). Overlay histogram showing HepG2 cells stained with A08719-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ATP4B Antibody (A08719-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-if-testing-7.jpgAnti-ATP4B Antibody Picoband® IF analysis of ATP4B using anti-ATP4B antibody (A08719-2). ATP4B was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ATP4B Antibody (A08719-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08719-2-atp4b-primary-antibodies-if-testing-8.jpgAnti-ATP4B Antibody Picoband® IF analysis of ATP4B using anti-ATP4B antibody (A08719-2). ATP4B was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ATP4B Antibody (A08719-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1257062026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07808-1-polr1d-primary-antibodies-wb-testing-1.jpgAnti-POLR1D Antibody Picoband® Western blot analysis of POLR1D using anti-POLR1D antibody (A07808-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLR1D antigen affinity purified polyclonal antibody (Catalog # A07808-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLR1D at approximately 20 kDa. The expected band size for POLR1D is at 15 kDa. https://www.bosterbio.com/catalog/product/view/id/1257072026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11611-2-polr3d-primary-antibodies-wb-testing-1.jpgAnti-POLR3D Antibody Picoband® Western blot analysis of POLR3D using anti-POLR3D antibody (A11611-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLR3D antigen affinity purified polyclonal antibody (Catalog # A11611-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLR3D at approximately 44 kDa. The expected band size for POLR3D is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11611-2-polr3d-primary-antibodies-ihc-testing-1.jpgAnti-POLR3D Antibody Picoband®IHC analysis of POLR3D using anti-POLR3D antibody (A11611-2). POLR3D was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POLR3D Antibody (A11611-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11611-2-polr3d-primary-antibodies-if-testing-2.jpgAnti-POLR3D Antibody Picoband® IF analysis of POLR3D using anti-POLR3D antibody (A11611-2) and anti-Beta Tubulin antibody (M01857-3). POLR3D was detected in immunocytochemical section of MCF-7 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POLR3D Antibody (A11611-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127)(B) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133)(D) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI(C). Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11611-2-polr3d-primary-antibodies-fcm-testing-3.pngAnti-POLR3D Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-POLR3D antibody (A11611-2). Overlay histogram showing 293T cells stained with A11611-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POLR3D Antibody (A11611-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257082026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11074-1-ppef1-primary-antibodies-wb-testing-1.jpgAnti-PPEF1 Antibody Picoband® Western blot analysis of PPEF1 using anti-PPEF1 antibody (A11074-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPEF1 antigen affinity purified polyclonal antibody (Catalog # A11074-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPEF1 at approximately 76 kDa. The expected band size for PPEF1 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11074-1-ppef1-primary-antibodies-if-testing-2.jpgAnti-PPEF1 Antibody Picoband® IF analysis of PPEF1 using anti-PPEF1 antibody (A11074-1). PPEF1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PPEF1 Antibody (A11074-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11074-1-ppef1-primary-antibodies-fcm-testing-3.pngAnti-PPEF1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PPEF1 antibody (A11074-1). Overlay histogram showing 293T cells stained with A11074-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPEF1 Antibody (A11074-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257092026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14650-1-ppp1r16a-primary-antibodies-wb-testing-1.jpgAnti-PPP1R16A Antibody Picoband® Western blot analysis of PPP1R16A using anti-PPP1R16A antibody (A14650-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP1R16A antigen affinity purified polyclonal antibody (Catalog # A14650-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPP1R16A at approximately 69 kDa. The expected band size for PPP1R16A is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14650-1-ppp1r16a-primary-antibodies-fcm-testing-2.pngAnti-PPP1R16A Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-PPP1R16A antibody (A14650-1). Overlay histogram showing U20S cells stained with A14650-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PPP1R16A Antibody (A14650-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257102026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14507-1-ppp1r37-primary-antibodies-wb-testing-1.jpgAnti-PPP1R37 Antibody Picoband® Western blot analysis of PPP1R37 using anti-PPP1R37 antibody (A14507-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP1R37 antigen affinity purified polyclonal antibody (Catalog # A14507-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPP1R37 at approximately 75 kDa. The expected band size for PPP1R37 is at 78 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14507-1-ppp1r37-primary-antibodies-fcm-testing-2.pngAnti-PPP1R37 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PPP1R37 antibody (A14507-1). Overlay histogram showing MCF-7 cells stained with A14507-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPP1R37 Antibody (A14507-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257112026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10833-1-ppp6r3-primary-antibodies-wb-testing-1.jpgAnti-SAPS3/PPP6R3 Antibody Picoband® Western blot analysis of SAPS3/PPP6R3 using anti-SAPS3/PPP6R3 antibody (A10833-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U-87MG whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat NRK whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SAPS3/PPP6R3 antigen affinity purified polyclonal antibody (Catalog # A10833-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SAPS3/PPP6R3 at approximately 144 kDa. The expected band size for SAPS3/PPP6R3 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10833-1-ppp6r3-primary-antibodies-if-testing-2.jpgAnti-SAPS3/PPP6R3 Antibody Picoband® IF analysis of PPP6R3 using anti-PPP6R3 antibody (A10833-1) and anti-Beta Tubulin antibody (M01857-3). PPP6R3 was detected in immunocytochemical section of MCF-7 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PPP6R3 Antibody (A10833-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10833-1-ppp6r3-primary-antibodies-fcm-testing-3.pngAnti-SAPS3/PPP6R3 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-SAPS3/PPP6R3 antibody (A10833-1). Overlay histogram showing Hela cells stained with A10833-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SAPS3/PPP6R3 Antibody (A10833-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257122026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14649-1-prox2-primary-antibodies-wb-testing-1.jpgAnti-PROX2 Antibody Picoband® Western blot analysis of PROX2 using anti-PROX2 antibody (A14649-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PROX2 antigen affinity purified polyclonal antibody (Catalog # A14649-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PROX2 at approximately 66 kDa. The expected band size for PROX2 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14649-1-prox2-primary-antibodies-if-testing-2.jpgAnti-PROX2 Antibody Picoband® IF analysis of PROX2 using anti-PROX2 antibody (A14649-1) and anti-Beta Tubulin antibody (M01857-3). PROX2 was detected in immunocytochemical section of MCF-7 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PROX2 Antibody (A14649-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14649-1-prox2-primary-antibodies-fcm-testing-3.pngAnti-PROX2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-PROX2 antibody (A14649-1). Overlay histogram showing HEL cells stained with A14649-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PROX2 Antibody (A14649-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257132026-03-17T05:15:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07461-1-ppp3cc-primary-antibodies-wb-testing-1.jpgAnti-PPP3CC Antibody Picoband® Western blot analysis of PPP3CC using anti-PPP3CC antibody (A07461-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: rat brain tissue lysates, Lane 5: rat skeletal muscle tissue lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPP3CC antigen affinity purified polyclonal antibody (Catalog # A07461-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PPP3CC at approximately 65 kDa. The expected band size for PPP3CC is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07461-1-ppp3cc-primary-antibodies-fcm-testing-2.pngAnti-PPP3CC Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PPP3CC antibody (A07461-1). Overlay histogram showing HepG2 cells stained with A07461-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PPP3CC Antibody (A07461-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257142026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11016-1-ndufb4-primary-antibodies-wb-testing-1.jpgAnti-NDUFB4 Antibody Picoband® Western blot analysis of NDUFB4 using anti-NDUFB4 antibody (A11016-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFB4 antigen affinity purified polyclonal antibody (Catalog # A11016-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NDUFB4 at approximately 15 kDa. The expected band size for NDUFB4 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11016-1-ndufb4-primary-antibodies-if-testing-2.jpgAnti-NDUFB4 Antibody Picoband® IF analysis of NDUFB4 using anti-NDUFB4 antibody (A11016-1). NDUFB4 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NDUFB4 Antibody (A11016-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11016-1-ndufb4-primary-antibodies-fcm-testing-3.pngAnti-NDUFB4 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-NDUFB4 antibody (A11016-1). Overlay histogram showing THP-1 cells stained with A11016-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NDUFB4 Antibody (A11016-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257152026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07499-1-psma5-primary-antibodies-wb-testing-1.jpgAnti-PSMA5 Antibody Picoband® Western blot analysis of PSMA5 using anti-PSMA5 antibody (A07499-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSMA5 antigen affinity purified polyclonal antibody (Catalog # A07499-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSMA5 at approximately 26 kDa. The expected band size for PSMA5 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07499-1-psma5-primary-antibodies-ihc-testing-1.jpgAnti-PSMA5 Antibody Picoband®IHC analysis of PSMA5 using anti-PSMA5 antibody (A07499-1). PSMA5 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSMA5 Antibody (A07499-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07499-1-psma5-primary-antibodies-if-testing-2.jpgAnti-PSMA5 Antibody Picoband® IF analysis of PSMA5 using anti-PSMA5 antibody (A07499-1). PSMA5 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PSMA5 Antibody (A07499-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07499-1-psma5-primary-antibodies-fcm-testing-3.pngAnti-PSMA5 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PSMA5 antibody (A07499-1). Overlay histogram showing Hela cells stained with A07499-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSMA5 Antibody (A07499-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257162026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05555-2-psmc1-primary-antibodies-wb-testing-1.jpgAnti-PSMC1 Antibody Picoband® Western blot analysis of PSMC1 using anti-PSMC1 antibody (A05555-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSMC1 antigen affinity purified polyclonal antibody (Catalog # A05555-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSMC1 at approximately 57 kDa. The expected band size for PSMC1 is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05555-2-psmc1-primary-antibodies-ihc-testing-1.jpgAnti-PSMC1 Antibody Picoband®IHC analysis of PSMC1 using anti-PSMC1 antibody (A05555-2). PSMC1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSMC1 Antibody (A05555-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05555-2-psmc1-primary-antibodies-if-testing-2.jpgAnti-PSMC1 Antibody Picoband® IF analysis of PSMC1 using anti-PSMC1 antibody (A05555-2) and anti-Beta Tubulin antibody (M01857-3). PSMC1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PSMC1 Antibody (A05555-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05555-2-psmc1-primary-antibodies-fcm-testing-3.pngAnti-PSMC1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PSMC1 antibody (A05555-2). Overlay histogram showing JK cells stained with A05555-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSMC1 Antibody (A05555-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257172026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-wb-testing-1.jpgAnti-NXPH3 Antibody Picoband® Western blot analysis of NXPD3 using anti-NXPD3 antibody (A14597-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NXPD3 antigen affinity purified polyclonal antibody (Catalog # A14597-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NXPD3 at approximately 28 kDa. The expected band size for NXPD3 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxph3-primary-antibodies-ihc-testing-6.jpgAnti-NXPH3 Antibody Picoband®IHC analysis of Neurexophilin 3/NXPH3 using anti-Neurexophilin 3/NXPH3 antibody (A14597-3). Neurexophilin 3/NXPH3 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Neurexophilin 3/NXPH3 Antibody (A14597-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-ihc-testing-2.jpgAnti-NXPH3 Antibody Picoband® IHC analysis of NXPD3 using anti-NXPD3 antibody (A14597-3). NXPD3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NXPD3 Antibody (A14597-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-ihc-testing-3.jpgAnti-NXPH3 Antibody Picoband® IHC analysis of NXPD3 using anti-NXPD3 antibody (A14597-3). NXPD3 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NXPD3 Antibody (A14597-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-ihc-testing-4.jpgAnti-NXPH3 Antibody Picoband® IHC analysis of NXPD3 using anti-NXPD3 antibody (A14597-3). NXPD3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NXPD3 Antibody (A14597-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-ihc-testing-5.jpgAnti-NXPH3 Antibody Picoband® IHC analysis of NXPD3 using anti-NXPD3 antibody (A14597-3). NXPD3 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NXPD3 Antibody (A14597-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-if-testing-6.jpgAnti-NXPH3 Antibody Picoband® IF analysis of NXPD3 using anti-NXPD3 antibody (A14597-3) and anti-Beta Tubulin antibody (M01857-3). NXPD3 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NXPD3 Antibody (A14597-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-fcm-testing-7.pngAnti-NXPH3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-NXPH3 antibody (A14597-3). Overlay histogram showing HepG2 cells stained with A14597-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NXPH3 Antibody (A14597-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14597-3-nxpd3-primary-antibodies-fcm-testing-8.pngAnti-NXPH3 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-NXPH3 antibody (A14597-3). Overlay histogram showing K562 cells stained with A14597-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NXPH3 Antibody (A14597-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257182026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09321-1-nrap-primary-antibodies-wb-testing-1.jpgAnti-NRAP Antibody Picoband® Western blot analysis of NRAP using anti-NRAP antibody (A09321-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat H9C2 whole cell lysates, Lane 2: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NRAP antigen affinity purified polyclonal antibody (Catalog # A09321-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NRAP at approximately 250 kDa. The expected band size for NRAP is at 197 kDa. https://www.bosterbio.com/catalog/product/view/id/1257192026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14864-1-nudt19-primary-antibodies-wb-testing-1.jpgAnti-NUDT19 Antibody Picoband® Western blot analysis of NUDT19 using anti-NUDT19 antibody (A14864-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT19 antigen affinity purified polyclonal antibody (Catalog # A14864-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDT19 at approximately 40 kDa. The expected band size for NUDT19 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14864-1-nudt19-primary-antibodies-ihc-testing-2.jpgAnti-NUDT19 Antibody Picoband® IHC analysis of NUDT19 using anti-NUDT19 antibody (A14864-1). NUDT19 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT19 Antibody (A14864-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14864-1-nudt19-primary-antibodies-ihc-testing-3.jpgAnti-NUDT19 Antibody Picoband® IHC analysis of NUDT19 using anti-NUDT19 antibody (A14864-1). NUDT19 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT19 Antibody (A14864-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14864-1-nudt19-primary-antibodies-ihc-testing-4.jpgAnti-NUDT19 Antibody Picoband® IHC analysis of NUDT19 using anti-NUDT19 antibody (A14864-1). NUDT19 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT19 Antibody (A14864-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14864-1-nudt19-primary-antibodies-ihc-testing-5.jpgAnti-NUDT19 Antibody Picoband® IHC analysis of NUDT19 using anti-NUDT19 antibody (A14864-1). NUDT19 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT19 Antibody (A14864-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14864-1-nudt19-primary-antibodies-fcm-testing-6.pngAnti-NUDT19 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NUDT19 antibody (A14864-1). Overlay histogram showing HEL cells stained with A14864-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDT19 Antibody (A14864-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1257212026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-wb-testing-1.jpgAnti-NDUFA9 Antibody Picoband® Western blot analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat RH35 whole cell lysates, Lane 4: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFA9 antigen affinity purified polyclonal antibody (Catalog # A07420-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NDUFA9 at approximately 36 kDa. The expected band size for NDUFA9 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-2.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-3.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-4.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-5.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-6.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-7.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-8.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-9.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-10.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-11.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-12.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-ihc-testing-13.jpgAnti-NDUFA9 Antibody Picoband® IHC analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-if-testing-14.jpgAnti-NDUFA9 Antibody Picoband® IF analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3) and anti-Beta Tubulin antibody (M01857-3). NDUFA9 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NDUFA9 Antibody (A07420-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-fcm-testing-15.pngAnti-NDUFA9 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-NDUFA9 antibody (A07420-3). Overlay histogram showing U87 cells stained with A07420-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NDUFA9 Antibody (A07420-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-if-testing-16.jpgAnti-NDUFA9 Antibody Picoband® IF analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07420-3-ndufa9-primary-antibodies-if-testing-17.jpgAnti-NDUFA9 Antibody Picoband® IF analysis of NDUFA9 using anti-NDUFA9 antibody (A07420-3). NDUFA9 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NDUFA9 Antibody (A07420-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1257222026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08298-mbnl3-primary-antibodies-wb-testing-1.jpgAnti-MBNL3 Antibody Picoband® Western blot analysis of MBNL3 using anti-MBNL3 antibody (A08298). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MBNL3 antigen affinity purified polyclonal antibody (Catalog # A08298) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MBNL3 at approximately 27 kDa. The expected band size for MBNL3 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08298-mbnl3-primary-antibodies-if-testing-2.jpgAnti-MBNL3 Antibody Picoband® IF analysis of MBNL3 using anti-MBNL3 antibody (A08298) and anti-Beta Tubulin antibody (M01857-3). MBNL3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MBNL3 Antibody (A08298) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1257232026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09822-med7-primary-antibodies-wb-testing-1.jpgAnti-MED7 Antibody Picoband® Western blot analysis of MED7 using anti-MED7 antibody (A09822). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED7 antigen affinity purified polyclonal antibody (Catalog # A09822) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED7 at approximately 27 kDa. The expected band size for MED7 is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09822-med7-primary-antibodies-if-testing-2.jpgAnti-MED7 Antibody Picoband® IF analysis of MED7 using anti-MED7 antibody (A09822) and anti-Beta Tubulin antibody (M01857-3). MED7 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MED7 Antibody (A09822) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09822-med7-primary-antibodies-ip-testing-1.jpgAnti-MED7 Antibody Picoband®Immunoprecipitating (IP) MED7 in PC-3 whole cell lysate. Western blot analysis of MED7 using anti-MED7 antibody (A09822); Lane 1: PC-3 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-MED7 antibody in PC-3 whole cell lysate; Lane 3: anti-MED7 antibody (2μg) + PC-3 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MED7 antigen affinity purified polyclonal antibody (A09822) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for MED7 at approximately 27 kDa. The expected band size for MED7 is at 27 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-abcd1-ald-rabbit-monoclonal-antibody-m01205-1-boster.html2026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01205-1-abcd1-primary-antibodies-wb-testing-1.jpgAnti-ABCD1 / ALD Rabbit Monoclonal AntibodyWestern blot analysis of ABCD1 using anti-ABCD1 antibody (M01205-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse liver tissue lysates, Lane 5: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCD1 antigen affinity purified monoclonal antibody (M01205-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ABCD1 at approximately 83 kDa. The expected band size for ABCD1 is at 83 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il18-binding-protein-rabbit-monoclonal-antibody-m07261-1-boster.html2026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07261-1-wb.jpgAnti-IL18 binding protein Rabbit Monoclonal AntibodyWestern blot analysis of IL18 binding protein in HeLa cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl2l15-rabbit-monoclonal-antibody-m14383-boster.html2026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14383-wb7.jpgAnti-BCL2L15 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14383-wb8.jpgAnti-BCL2L15 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14383-wb.jpgAnti-BCL2L15 Rabbit Monoclonal AntibodyWestern blot analysis of BCL2L15 in His-tagged BCL2L15 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rip2-rabbit-monoclonal-antibody-m00818-boster.html2026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00818-wb.jpgAnti-RIP2 Rabbit Monoclonal AntibodyWestern blot analysis of RIP2 in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00818-ripk2-primary-antibodies-ihc-testing-1.jpgAnti-RIP2 Rabbit Monoclonal AntibodyIHC analysis of RIPK2 using anti-RIPK2 antibody (M00818). RIPK2 was detected in a paraffin-embedded section of human colon. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.06, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with rabbit anti-RIPK2 Antibody (M00818) at a dilution of 1:100 overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00818-ripk2-primary-antibodies-ihc-testing-2.jpgAnti-RIP2 Rabbit Monoclonal AntibodyIHC analysis of RIPK2 using anti-RIPK2 antibody (M00818). RIPK2 was detected in a paraffin-embedded section of human colon cancer. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0 6, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with rabbit anti-RIPK2 Antibody (M00818) at a dilution of 1:100 overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd275-rabbit-monoclonal-antibody-m01965-1-boster.html2026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01965-1-wb.jpgAnti-CD275 Rabbit Monoclonal AntibodyWestern blot analysis of CD275 in HUVEC cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rala-rabbit-monoclonal-antibody-m04677-boster.html2026-03-17T05:15:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04677-wb.jpgAnti-RalA Rabbit Monoclonal AntibodyWestern blot analysis of RalA in MCF7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04677-wb7.jpgAnti-RalA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cathepsin-h-rabbit-monoclonal-antibody-m01510-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01510-wb.jpgAnti-Cathepsin H Rabbit Monoclonal AntibodyWestern blot analysis of Cathepsin H in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01510-wb7.jpgAnti-Cathepsin H Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-htra1-rabbit-monoclonal-antibody-m01801-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01801-wb.jpgAnti-htrA1 Rabbit Monoclonal AntibodyWestern blot analysis of htrA1 in MCF7 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il15-rabbit-monoclonal-antibody-m00212-1-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00212-1-wb.jpgAnti-IL15 Rabbit Monoclonal AntibodyWestern blot analysis of IL15 in Recombinant human IL-15 protein cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ube1l-uba7-rabbit-monoclonal-antibody-m08637-2-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08637-2-wb.jpgAnti-Ube1L / UBA7 Rabbit Monoclonal AntibodyWestern blot analysis of Ube1L / UBA7 in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08637-2-wb7.jpgAnti-Ube1L / UBA7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il22-rabbit-monoclonal-antibody-m00963-1-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00963-1-wb.jpgAnti-IL22 Rabbit Monoclonal AntibodyWestern blot analysis of IL22 in Recombinant Human IL22 protein cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il9-rabbit-monoclonal-antibody-m02925-1-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02925-1-wb.jpgAnti-IL9 Rabbit Monoclonal AntibodyWestern blot analysis of IL9 in Recombinant Human IL9 protein cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il26-rabbit-monoclonal-antibody-m07565-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07565-wb.jpgAnti-IL26 Rabbit Monoclonal AntibodyWestern blot analysis of IL26 in His-tagged IL26 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd116-rabbit-monoclonal-antibody-m04432-1-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04432-1-wb.jpgAnti-CD116 Rabbit Monoclonal AntibodyWestern blot analysis of CD116 in 293 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il12b-rabbit-monoclonal-antibody-m01152-3-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01152-3-wb.jpgAnti-IL12B Rabbit Monoclonal AntibodyWestern blot analysis of IL12B in Recombinant Human IL12B protein cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01152-3-wb9.jpgAnti-IL12B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01152-3-wb7.jpgAnti-IL12B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01152-3-wb8.jpgAnti-IL12B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd125-rabbit-monoclonal-antibody-m04243-boster.html2026-03-17T05:15:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04243-wb.jpgAnti-CD125 Rabbit Monoclonal AntibodyWestern blot analysis of CD125 in Human serum cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-s198-rabbit-monoclonal-antibody-m00097s198-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s198-wb7.jpgAnti-Phospho-Tau (S198) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s198-wb.jpgAnti-Phospho-Tau (S198) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Tau (S198) expression in mouse hippocampus cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-jak1-y1034-y1035-rabbit-monoclonal-antibody-m00330y1034y1035-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00330y1034y1035-wb.jpgAnti-Phospho-JAK1 (Y1034 + Y1035) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-JAK1 (Y1034 + Y1035) expression in Ramos treated with pervanadate cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gamma-glutamyl-hydrolase-rabbit-monoclonal-antibody-m03161-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03161-wb7.jpgAnti-Gamma glutamyl hydrolase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03161-wb9.jpgAnti-Gamma glutamyl hydrolase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03161-wb8.jpgAnti-Gamma glutamyl hydrolase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03161-wb.jpgAnti-Gamma glutamyl hydrolase Rabbit Monoclonal AntibodyWestern blot analysis of Gamma glutamyl hydrolase expression in MCF7 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dopamine-beta-hydroxylase-rabbit-monoclonal-antibody-m01110-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01110-wb.jpgAnti-Dopamine beta Hydroxylase Rabbit Monoclonal AntibodyWestern blot analysis of Dopamine beta Hydroxylase expression in SH-SY5Y cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-s199-rabbit-monoclonal-antibody-m00097s199-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s199-wb.jpgAnti-Phospho-Tau (S199) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Tau (S199) expression in mouse hippocampus cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-s404-rabbit-monoclonal-antibody-m00097s404-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s404-p-tau-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Tau (S404) Rabbit Monoclonal AntibodyWestern blot analysis of P-TAU(S404) using anti-P-TAU(S404) antibody (M00097S404). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-TAU(S404) antigen affinity purified monoclonal antibody (M00097S404) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-TAU(S404) at approximately 50 kDa. The expected band size for P-TAU(S404) is at 79 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-s214-rabbit-monoclonal-antibody-m00097s214-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s214-wb7.jpgAnti-Phospho-Tau (S214) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s214-wb8.jpgAnti-Phospho-Tau (S214) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s214-wb.jpgAnti-Phospho-Tau (S214) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Tau (S214) expression in mouse cerebral cortex cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-s202-rabbit-monoclonal-antibody-m00097s202-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s202-wb7.jpgAnti-Phospho-Tau (S202) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s202-wb8.jpgAnti-Phospho-Tau (S202) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097s202-wb.jpgAnti-Phospho-Tau (S202) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Tau (S202) expression in mouse hippocampus cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gas2-rabbit-monoclonal-antibody-m08589-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08589-wb7.jpgAnti-GAS2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08589-wb.jpgAnti-GAS2 Rabbit Monoclonal AntibodyWestern blot analysis of GAS2 expression in Jurkat cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-akt1-akt2-akt3-rabbit-monoclonal-antibody-m00024-7-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00024-7-wb7.jpgAnti-AKT1 + AKT2 + AKT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00024-7-icc2.jpgAnti-AKT1 + AKT2 + AKT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00024-7-wb8.jpgAnti-AKT1 + AKT2 + AKT3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00024-7-icc3.jpgAnti-AKT1 + AKT2 + AKT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00024-7-icc1.jpgAnti-AKT1 + AKT2 + AKT3 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00024-7-wb.jpgAnti-AKT1 + AKT2 + AKT3 Rabbit Monoclonal AntibodyWestern blot analysis of AKT1 + AKT2 + AKT3 expression in (1) Hela cell lysate;(2) A549 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00024-7-ip7.jpgAnti-AKT1 + AKT2 + AKT3 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution) https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-il13-rabbit-monoclonal-antibody-m00077-1-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-1-wb.jpgAnti-IL13 Rabbit Monoclonal AntibodyWestern blot analysis of IL13 expression in human recombinant protein cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-camkii-alpha-t286-rabbit-monoclonal-antibody-m03241t286-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03241t286-wb7.jpgAnti-Phospho-CaMKII alpha (T286) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03241t286-wb8.jpgAnti-Phospho-CaMKII alpha (T286) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03241t286-wb.jpgAnti-Phospho-CaMKII alpha (T286) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-CaMKII alpha (T286) expression in Mouse brain treated with Lambda phosphatase cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hn1-rabbit-monoclonal-antibody-m31925-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31925-wb7.jpgAnti-HN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31925-icc2.jpgAnti-HN1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31925-wb8.jpgAnti-HN1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31925-icc3.jpgAnti-HN1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31925-icc1.jpgAnti-HN1 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31925-wb.jpgAnti-HN1 Rabbit Monoclonal AntibodyWestern blot analysis of HN1 expression in HeLa cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dcr1-cd263-rabbit-monoclonal-antibody-m04218-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04218-wb.jpgAnti-DcR1 / CD263 Rabbit Monoclonal AntibodyWestern blot analysis of DcR1/CD263 expression in Jurkat cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-eif3a-rabbit-monoclonal-antibody-m02339-boster.html2026-03-17T05:15:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02339-icc1.jpgAnti-eIF3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02339-icc4.jpgAnti-eIF3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02339-icc2.jpgAnti-eIF3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02339-wb.jpgAnti-eIF3A Rabbit Monoclonal AntibodyWestern blot analysis of eIF3A expression in Jurkat cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02339-icc3.jpgAnti-eIF3A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ulk1-s556-rabbit-monoclonal-antibody-m00584s556-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584s556-p-ulk1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-ULK1 (S556) Rabbit Monoclonal Antibody Western blot analysis of ULK1 using anti-ULK1 antibody (M00584S556). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ULK1 antigen affinity purified monoclonal antibody (Catalog # M00584S556) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ULK1 at approximately 150 kDa. The expected band size for ULK1 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584s556-icc2.jpgAnti-Phospho-ULK1 (S556) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00584s556-icc1.jpgAnti-Phospho-ULK1 (S556) Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-gsta4-rabbit-monoclonal-antibody-m03699-1-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03699-1-wb.jpgAnti-GSTA4 Rabbit Monoclonal AntibodyWestern blot analysis of GSTA4 expression in 293T cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03699-1-wb7.jpgAnti-GSTA4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sec14l2-tap-rabbit-monoclonal-antibody-m06211-1-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06211-1-wb7.jpgAnti-SEC14L2 / TAP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06211-1-icc3.jpgAnti-SEC14L2 / TAP Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06211-1-icc1.jpgAnti-SEC14L2 / TAP Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06211-1-wb.jpgAnti-SEC14L2 / TAP Rabbit Monoclonal AntibodyWestern blot analysis of SEC14L2 / TAP expression in U87-MG cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06211-1-icc2.jpgAnti-SEC14L2 / TAP Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nfe2-rabbit-monoclonal-antibody-m03765-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03765-wb7.jpgAnti-NFE2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03765-wb.jpgAnti-NFE2 Rabbit Monoclonal AntibodyWestern blot analysis of NFE2 expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03765-wb8.jpgAnti-NFE2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03765-ip7.jpgAnti-NFE2 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03765-icc1.jpgAnti-NFE2 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pdgf-b-rabbit-monoclonal-antibody-m00348-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00348-wb7.jpgAnti-PDGF B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00348-wb.jpgAnti-PDGF B Rabbit Monoclonal AntibodyWestern blot analysis of PDGF B expression in A375 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00348-wb8.jpgAnti-PDGF B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00348-wb9.jpgAnti-PDGF B Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-vimentin-s39-rabbit-monoclonal-antibody-m00235s39-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235s39-wb7.jpgAnti-Phospho-Vimentin (S39) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235s39-wb8.jpgAnti-Phospho-Vimentin (S39) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00235s39-wb.jpgAnti-Phospho-Vimentin (S39) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Vimentin (S39) expression in HeLa treated with Calyculin A cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-rip3-s232-rabbit-monoclonal-antibody-m00202s232-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00202s232-rip3-primary-antibodies-wb-testing-1.jpgAnti-Phospho-RIP3 (S232) Rabbit Monoclonal Antibody Western blot analysis of Phospho-RIP3 (S232) using anti-Phospho-RIP3 (S232) antibody (M00202S232). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat spleen tissue lysates, Lane 2: rat liver tissue lysates, Lane 3: rat heart tissue lysates, Lane 4: rat L6 whole cell lysates, Lane 5: mouse spleen tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse L929 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-RIP3 (S232) antigen affinity purified monoclonal antibody (Catalog # M00202S232) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Phospho-RIP3 (S232) at approximately 50 kDa. The expected band size for Phospho-RIP3 (S232) is at 50 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nr2c2-tr4-rabbit-monoclonal-antibody-m02752-1-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02752-1-wb.jpgAnti-NR2C2 / TR4 Rabbit Monoclonal AntibodyWestern blot analysis of NR2C2/TR4 expression in PC-3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02752-1-wb10.jpgAnti-NR2C2 / TR4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02752-1-wb8.jpgAnti-NR2C2 / TR4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02752-1-wb11.jpgAnti-NR2C2 / TR4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02752-1-wb9.jpgAnti-NR2C2 / TR4 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ptbp2-rabbit-monoclonal-antibody-m05020-3-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-3-wb7.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05020-3-wb.jpgAnti-PTBP2 Rabbit Monoclonal AntibodyWestern blot analysis of PTBP2 expression in Neuro2a cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lunatic-fringe-rabbit-monoclonal-antibody-m04513-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04513-icc1.jpgAnti-Lunatic Fringe Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04513-wb.jpgAnti-Lunatic Fringe Rabbit Monoclonal AntibodyWestern blot analysis of Lunatic Fringe expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04513-icc2.jpgAnti-Lunatic Fringe Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04513-icc3.jpgAnti-Lunatic Fringe Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:500 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-timm22-rabbit-monoclonal-antibody-m15312-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m15312-wb7.jpgAnti-TIMM22 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m15312-wb.jpgAnti-TIMM22 Rabbit Monoclonal AntibodyWestern blot analysis of TIMM22 expression in A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m15312-wb8.jpgAnti-TIMM22 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m15312-wb9.jpgAnti-TIMM22 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hoxc6-rabbit-monoclonal-antibody-m06045-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06045-hoxc6-primary-antibodies-wb-testing-1.jpgAnti-HoxC6 Rabbit Monoclonal Antibody Western blot analysis of HoxC6 using anti-HoxC6 antibody (M06045). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HoxC6 antigen affinity purified monoclonal antibody (Catalog # M06045) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HoxC6 at approximately 26,27 kDa. The expected band size for HoxC6 is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06045-icc1.jpgAnti-HoxC6 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06045-icc2.jpgAnti-HoxC6 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06045-icc3.jpgAnti-HoxC6 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06045-icc4.jpgAnti-HoxC6 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06045-icc5.jpgAnti-HoxC6 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06045-icc6.jpgAnti-HoxC6 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-lrp6-s1490-rabbit-monoclonal-antibody-m00970s1490-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00970s1490-wb.jpgAnti-Phospho-LRP6 (S1490) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-LRP6 (S1490) expression in heLa treated with Calyculin cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-erbb2-y1221-y1222-rabbit-monoclonal-antibody-m00010y1221y1222-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010y1221y1222-wb.jpgAnti-Phospho-ErbB2(Y1221 + Y1222) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-ErbB2(Y1221 + Y1222) expression in SKBR3 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-rb-s780-rabbit-monoclonal-antibody-m00039s780-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039s780-wb7.jpgAnti-Phospho-Rb (S780) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00039s780-wb.jpgAnti-Phospho-Rb (S780) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Rb (S780) expression in K562 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-egfr-y845-rabbit-monoclonal-antibody-m00023y845-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023y845-wb.jpgAnti-Phospho-EGFR (Y845) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-EGFR (Y869) expression in A431 treated with EGF cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-chk1-s280-rabbit-monoclonal-antibody-m01060s280-boster.html2026-03-17T05:15:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01060s280-wb7.jpgAnti-Phospho-Chk1 (S280) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01060s280-wb.jpgAnti-Phospho-Chk1 (S280) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Chk1 (S280) expression in 293T treated with Calyculin A cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-as160-t642-rabbit-monoclonal-antibody-m02004t642-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02004t642-wb.jpgAnti-Phospho-AS160 (T642) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-AS160 (T642) expression in 293T treated with insulin cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hspc150-rabbit-monoclonal-antibody-m05874-1-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05874-1-wb7.jpgAnti-HSPC150 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05874-1-wb.jpgAnti-HSPC150 Rabbit Monoclonal AntibodyWestern blot analysis of HSPC150 expression in HeLa cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-exoc2-rabbit-monoclonal-antibody-m04913-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04913-wb7.jpgAnti-EXOC2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04913-wb8.jpgAnti-EXOC2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04913-wb.jpgAnti-EXOC2 Rabbit Monoclonal AntibodyWestern blot analysis of EXOC2 expression in BxPC-3 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-dut-rabbit-monoclonal-antibody-m04280-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04280-wb7.jpgAnti-DUT Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04280-icc2.jpgAnti-DUT Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04280-wb.jpgAnti-DUT Rabbit Monoclonal AntibodyWestern blot analysis of DUT expression in Ramos cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04280-icc1.jpgAnti-DUT Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rab22a-rabbit-monoclonal-antibody-m05967-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05967-wb7.jpgAnti-RAB22A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05967-icc1.jpgAnti-RAB22A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05967-wb8.jpgAnti-RAB22A Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05967-icc2.jpgAnti-RAB22A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05967-wb.jpgAnti-RAB22A Rabbit Monoclonal AntibodyWestern blot analysis of RAB22A expression in (1) MCF-7 cell lysate; (2) BxPC-3 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05967-icc3.jpgAnti-RAB22A Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05967-ip7.jpgAnti-RAB22A Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution) https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cxcr6-cd186-rabbit-monoclonal-antibody-m02517-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02517-wb7.jpgAnti-CXCR6 / CD186 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02517-wb.jpgAnti-CXCR6 / CD186 Rabbit Monoclonal AntibodyWestern blot analysis of CXCR6/CD186 expression in JAR cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02517-wb8.jpgAnti-CXCR6 / CD186 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02517-wb9.jpgAnti-CXCR6 / CD186 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tfiie-alpha-rabbit-monoclonal-antibody-m11288-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11288-wb7.jpgAnti-TFIIE alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11288-icc1.jpgAnti-TFIIE alpha Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11288-wb8.jpgAnti-TFIIE alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11288-icc2.jpgAnti-TFIIE alpha Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11288-wb.jpgAnti-TFIIE alpha Rabbit Monoclonal AntibodyWestern blot analysis of TFIIE alpha expression in HeLa cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hrpt2-cdc73-rabbit-monoclonal-antibody-m01726-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01726-wb8.jpgAnti-HRPT2 / CDC73 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01726-wb.jpgAnti-HRPT2 / CDC73 Rabbit Monoclonal AntibodyWestern blot analysis of HRPT2/CDC73 expression in 293T cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-palladin-rabbit-monoclonal-antibody-m04005-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04005-wb7.jpgAnti-Palladin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04005-wb8.jpgAnti-Palladin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04005-wb.jpgAnti-Palladin Rabbit Monoclonal AntibodyWestern blot analysis of Palladin expression in PC3 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-desmocollin-1-rabbit-monoclonal-antibody-m03478-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03478-wb7.jpgAnti-Desmocollin 1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03478-wb8.jpgAnti-Desmocollin 1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03478-wb.jpgAnti-Desmocollin 1 Rabbit Monoclonal AntibodyWestern blot analysis of Desmocollin 1 expression in A375 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c1qa-rabbit-monoclonal-antibody-m01955-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01955-c1qa-primary-antibodies-wb-testing-1.jpgAnti-C1QA Rabbit Monoclonal AntibodyWestern blot analysis of C1QA using anti-C1QA antibody (M01955). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HCCT whole cell lysates, Lane 2: human HCCP whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C1QA antigen affinity purified monoclonal antibody (M01955) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for C1QA at approximately 28 kDa. The expected band size for C1QA is at 28 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd223-rabbit-monoclonal-antibody-m02869-3-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-3-icc1.jpgAnti-CD223 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-3-icc2.jpgAnti-CD223 Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:150 dilution. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd163l1-rabbit-monoclonal-antibody-m09845-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09845-cd163l1-primary-antibodies-ihc-testing-1.jpgAnti-CD163L1 Rabbit Monoclonal AntibodyFigure 1. IHC analysis of CD163b/CD163L1 using anti-CD163b/CD163L1 antibody (M09845). CD163b/CD163L1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CD163b/CD163L1 Antibody (M09845) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09845-cd163l1-primary-antibodies-ihc-testing-2.jpgAnti-CD163L1 Rabbit Monoclonal AntibodyFigure 2. IHC analysis of CD163b/CD163L1 using anti-CD163b/CD163L1 antibody (M09845). CD163b/CD163L1 was detected in a paraffin-embedded section of human appendix tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CD163b/CD163L1 Antibody (M09845) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cabp-rabbit-monoclonal-antibody-m04165-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04165-wb7.jpgAnti-CABP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04165-icc1.jpgAnti-CABP Rabbit Monoclonal AntibodyImmunofluorescent analysis using the Antibody at 1:50 dilution.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04165-wb8.jpgAnti-CABP Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04165-wb.jpgAnti-CABP Rabbit Monoclonal AntibodyWestern blot analysis of CABP expression in U-87 MG cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-shb-rabbit-monoclonal-antibody-m02109-boster.html2026-03-17T05:15:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02109-wb.jpgAnti-SHB Rabbit Monoclonal AntibodyWestern blot analysis of SHB expression in K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02109-wb7.jpgAnti-SHB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:8K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ceruloplasmin-rabbit-monoclonal-antibody-m02883-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02883-wb.jpgAnti-Ceruloplasmin Rabbit Monoclonal AntibodyWestern blot analysis of Ceruloplasmin expression in Rat liver cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02883-wb7.jpgAnti-Ceruloplasmin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tbp7-rabbit-monoclonal-antibody-m06099-1-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06099-1-wb.jpgAnti-Tbp7 Rabbit Monoclonal AntibodyWestern blot analysis of Tbp7 expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06099-1-wb7.jpgAnti-Tbp7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06099-1-wb8.jpgAnti-Tbp7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sec62-rabbit-monoclonal-antibody-m05906-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05906-sec62-primary-antibodies-wb-testing-1.jpgAnti-SEC62 Rabbit Monoclonal AntibodyWestern blot analysis of SEC62 using anti-SEC62 antibody (M05906). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human SH-SY5Y whole cell lysates, Lane 6: mouse lung tissue lysates, Lane 7: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SEC62 antigen affinity purified monoclonal antibody (M05906) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SEC62 at approximately 50 kDa. The expected band size for SEC62 is at 50 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lap3-rabbit-monoclonal-antibody-m01921-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01921-wb.jpgAnti-LAP3 Rabbit Monoclonal AntibodyWestern blot analysis of LAP3 expression in 293T cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-psip1-ledgf-rabbit-monoclonal-antibody-m01960-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01960-wb.jpgAnti-PSIP1 / LEDGF Rabbit Monoclonal AntibodyWestern blot analysis of PSIP1 / LEDGF expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01960-wb7.jpgAnti-PSIP1 / LEDGF Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-fetuin-b-rabbit-monoclonal-antibody-m09065-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09065-wb.jpgAnti-Fetuin B Rabbit Monoclonal AntibodyWestern blot analysis of Fetuin B expression in human serum cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-somatostatin-28-rabbit-monoclonal-antibody-m01297-boster.html2026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01297-sst-primary-antibodies-ihc-testing-1.jpgAnti-Somatostatin 28 Rabbit Monoclonal AntibodyIHC analysis of Somatostatin 28 using anti-Somatostatin 28 antibody (M01297). Somatostatin 28 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Somatostatin 28 Antibody (M01297) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01297-sst-primary-antibodies-ihc-testing-2.jpgAnti-Somatostatin 28 Rabbit Monoclonal AntibodyIHC analysis of Somatostatin 28 using anti-Somatostatin 28 antibody (M01297). Somatostatin 28 was detected in a paraffin-embedded section of mouse pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Somatostatin 28 Antibody (M01297) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01297-sst-primary-antibodies-ihc-testing-3.jpgAnti-Somatostatin 28 Rabbit Monoclonal AntibodyIHC analysis of Somatostatin 28 using anti-Somatostatin 28 antibody (M01297). Somatostatin 28 was detected in a paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Somatostatin 28 Antibody (M01297) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hcg-beta-rabbit-monoclonal-antibody-m14647-boster.html2026-03-17T05:15:53+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tripeptidyl-peptidase-ii-rabbit-monoclonal-antibody-m06668-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06668-wb.jpgAnti-Tripeptidyl peptidase II Rabbit Monoclonal AntibodyWestern blot analysis of Tripeptidyl peptidase II expression in HepG2 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-aldh2-rabbit-monoclonal-antibody-m00546-5-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00546-5-wb7.jpgAnti-ALDH2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00546-5-wb.jpgAnti-ALDH2 Rabbit Monoclonal AntibodyWestern blot analysis of ALDH2 expression in HepG2 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00546-5-wb8.jpgAnti-ALDH2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00546-5-wb9.jpgAnti-ALDH2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2b-crotonyl-k12-rabbit-monoclonal-antibody-m07286-4-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-4-wb7.jpgAnti-Histone H2B (crotonyl K12) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-4-wb10.jpgAnti-Histone H2B (crotonyl K12) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-4-wb8.jpgAnti-Histone H2B (crotonyl K12) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-4-wb11.jpgAnti-Histone H2B (crotonyl K12) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-4-wb9.jpgAnti-Histone H2B (crotonyl K12) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-4-wb.jpgAnti-Histone H2B (crotonyl K12) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2B (crotonyl K12) expression in HeLa cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-iba1-rabbit-monoclonal-antibody-m01394-4-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01394-4-4-aif1-primary-antibodies-wb-testing-1.jpgAnti-Iba1 Rabbit Monoclonal AntibodyWestern blot analysis of IBA1/AIF1 using anti-IBA1/AIF1 antibody (M01394-4). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat spleen tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IBA1/AIF1 antigen affinity purified monoclonal antibody (M01394-4) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IBA1/AIF1 at approximately 17 kDa. The expected band size for IBA1/AIF1 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01394-4-aif1-primary-antibodies-ihc-testing-1.jpgAnti-Iba1 Rabbit Monoclonal AntibodyIHC analysis of IBA1/AIF1 using anti-IBA1/AIF1 antibody (M01394-4). IBA1/AIF1 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-IBA1/AIF1 Antibody (M01394-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01394-4-aif1-primary-antibodies-ihc-testing-2.jpgAnti-Iba1 Rabbit Monoclonal AntibodyIHC analysis of IBA1/AIF1 using anti-IBA1/AIF1 antibody (M01394-4). IBA1/AIF1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-IBA1/AIF1 Antibody (M01394-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01394-4-aif1-primary-antibodies-ihc-testing-3.jpgAnti-Iba1 Rabbit Monoclonal AntibodyIHC analysis of IBA1/AIF1 using anti-IBA1/AIF1 antibody (M01394-4). IBA1/AIF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-IBA1/AIF1 Antibody (M01394-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01394-4-aif1-primary-antibodies-ihc-testing-4.jpgAnti-Iba1 Rabbit Monoclonal AntibodyIHC analysis of IBA1/AIF1 using anti-IBA1/AIF1 antibody (M01394-4). IBA1/AIF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-IBA1/AIF1 Antibody (M01394-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01394-4-aif1-primary-antibodies-if-testing-1.pngAnti-Iba1 Rabbit Monoclonal AntibodyIF analysis of Alpha-Smooth Muscle Actin using anti-Alpha-Smooth Muscle Actin antibody (MA1106). Alpha-Smooth Muscle Actin was detected in a paraffin-embedded section of mouse cerebral infarction tissue. tissue . Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 mouse anti-Alpha-Smooth Muscle Actin Antibody (MA1106) overnight at 4°C. Goat Anti-Rabbit IgG (H+L) Secondary Antibody, Fluoro594 Conjugated (BA1142) was used as secondary antibody incubated with 1:500 and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-choline-acetyltransferase-rabbit-monoclonal-antibody-m01192-2-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01192-2-wb7.jpgAnti-Choline Acetyltransferase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01192-2-wb.jpgAnti-Choline Acetyltransferase Rabbit Monoclonal AntibodyWestern blot analysis of Choline Acetyltransferase expression in Mouse brain cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p38-t180-rabbit-monoclonal-antibody-m00176t180-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176t180-wb.jpgAnti-Phospho-p38 (T180) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-p38 (T180) expression in HeLa treated with anisomycin cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00176t180-wb7.jpgAnti-Phospho-p38 (T180) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkc-delta-pkc-theta-rabbit-monoclonal-antibody-m00822-2-boster.html2026-03-17T05:15:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00822-2-prkcd-primary-antibodies-wb-testing-1.jpgAnti-PKC delta + PKC theta Rabbit Monoclonal AntibodyWestern blot analysis of PRKCD using anti-PRKCD antibody (M00822-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat lung tissue lysates, Lane 4: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRKCD antigen affinity purified monoclonal antibody (M00822-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PRKCD at approximately 78 kDa. The expected band size for PRKCD is at 78 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-bcl-xl-rabbit-monoclonal-antibody-m00181-3-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-3-wb.jpgAnti-Bcl-XL Rabbit Monoclonal AntibodyWestern blot analysis of Bcl-XL expression in (1) Ramos cell lysate; (2) K562 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-3-wb9.jpgAnti-Bcl-XL Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-3-wb7.jpgAnti-Bcl-XL Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00181-3-wb8.jpgAnti-Bcl-XL Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-alpha-tubulin-acetyl-k40-rabbit-monoclonal-antibody-m08382-6-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-6-wb.jpgAnti-alpha Tubulin (acetyl K40) Rabbit Monoclonal AntibodyWestern blot analysis of alpha Tubulin (acetyl K40) expression in Mouse spleen cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-6-wb7.jpgAnti-alpha Tubulin (acetyl K40) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08382-6-wb8.jpgAnti-alpha Tubulin (acetyl K40) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-k27-linkage-specific-ubiquitin-rabbit-monoclonal-antibody-m02848-5-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02848-5-wb.jpgAnti-K27-linkage Specific Ubiquitin Rabbit Monoclonal AntibodyWestern blot analysis of K27-linkage Specific Ubiquitin expression in HeLa cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h4-mono-methyl-k20-rabbit-monoclonal-antibody-m14495-13-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-13-wb.jpgAnti-Histone H4 (mono methyl K20) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H4 (mono methyl K20) expression in Hela cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-13-wb7.jpgAnti-Histone H4 (mono methyl K20) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-13-wb8.jpgAnti-Histone H4 (mono methyl K20) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-histone-h3-s10-rabbit-monoclonal-antibody-m12477s10-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477s10-wb.jpgAnti-Phospho-Histone H3 (S10) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Histone H3 (S10) expression in HeLa treated Colcemid cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-symmetric-di-methyl-r17-rabbit-monoclonal-antibody-m12477-17-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-17-wb.jpgAnti-Histone H3 (symmetric di methyl R17) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (symmetric di methyl R17) expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-17-wb7.jpgAnti-Histone H3 (symmetric di methyl R17) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-di-methyl-k79-rabbit-monoclonal-antibody-m12477-18-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-18-wb.jpgAnti-Histone H3 (di methyl K79) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (di methyl K79) expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-18-wb7.jpgAnti-Histone H3 (di methyl K79) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-18-wb8.jpgAnti-Histone H3 (di methyl K79) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2a-mono-methyl-k118-rabbit-monoclonal-antibody-m16777-5-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-5-wb.jpgAnti-Histone H2A (mono methyl K118) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2A (mono methyl K118) expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m16777-5-wb7.jpgAnti-Histone H2A (mono methyl K118) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-apc6-cdc16-rabbit-monoclonal-antibody-m04573-1-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04573-1-wb7.jpgAnti-Apc6 / CDC16 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:4K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04573-1-wb.jpgAnti-Apc6 / CDC16 Rabbit Monoclonal AntibodyWestern blot analysis of Apc6 / CDC16 expression in HepG2 cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hsp70-rabbit-monoclonal-antibody-m01024-4-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-4-hsc70-primary-antibodies-wb-testing-1.jpgAnti-Hsp70 Rabbit Monoclonal Antibody Western blot analysis of Hsp70 using anti-Hsp70 antibody (M01024-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Hsp70 antigen affinity purified monoclonal antibody (Catalog # M01024-4) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Hsp70 at approximately 70 kDa. The expected band size for Hsp70 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01024-4-ip7.jpgAnti-Hsp70 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution) https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-hif-1-alpha-rabbit-monoclonal-antibody-m00013-4-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00013-4-hif-1_-primary-antibodies-wb-testing-1.jpgAnti-HIF-1-alpha Rabbit Monoclonal Antibody Western blot analysis of HIF-1-Alpha using anti-HIF-1-Alpha antibody (M00013-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HIF-1-Alpha antigen affinity purified monoclonal antibody (Catalog # M00013-4) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HIF-1-Alpha at approximately 110 kDa. The expected band size for HIF-1-Alpha is at 110 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00013-4-wb7.jpgAnti-HIF-1-alpha Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00013-4-40752108-figure-2.jpgAnti-HIF-1-alpha Rabbit Monoclonal Antibody(H) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, 4EBP1, FLAG, and HIF-1α in liver tissues analyzed using western blotting. (I) Immunofluorescence double staining of α-SMA and HIF-1α in the liver sections of mice (×100 magnification). The arrow heads represent colocalization of staining. (J) Relative quantification of α-SMA, HIF-1α, and colocalization of α-SMA and HIF-1α. EV, AAV2/8-scramble; OE, AAV2/8-4ebp1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; AAV, adeno-associated virus; ALT, alanine aminotransferase; AST, aspartate aminotransferase; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin and eosin; HIF-1α, hypoxia inducible factor 1 subunit alpha; IL-6, interleukin 6; RT-qPCR, quantitative reverse transcription polymerase chain reaction; TGF-β1, transforming growth factor beta 1. Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00013-4-40752108-figure-3.jpgAnti-HIF-1-alpha Rabbit Monoclonal Antibody(F) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, 4EBP1, FLAG, and HIF-1α in liver tissues was analyzed using western blotting. (G) Immunofluorescence double staining of α-SMA and HIF-1α in the liver sections of mice (×100 magnification). The arrowheads represent colocalization of staining. (H) Relative quantification of α-SMA, HIF-1α, and colocalization of α-SMA and HIF-1α. EV, AAV2/8-scramble; OE, AAV2/8-4ebp1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; AAV, adeno-associated virus; ALT, alanine aminotransferase; AST, aspartate aminotransferase; BDL, bile duct ligation; DAPI, 4′,6-diamidino-2-phenylindole; DBIL, direct bilirubin; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; H&E, hematoxylin-eosin; HIF-1α, hypoxia inducible factor 1 subunit alpha; IL-6, Interleukin 6; TBIL, total bilirubin; TGF-β1, transforming growth factor beta 1. Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00013-4-40752108-figure-5.jpgAnti-HIF-1-alpha Rabbit Monoclonal Antibody(I) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, 4EBP1, FLAG, and HIF-1α in LX-2 cells analyzed using western blotting. (J) Immunofluorescence double staining of α-SMA and HIF-1α in vehicle or TGF-β1-stimulated LX-2 cells transducted with LV-empty or LV-4EBP1-4A-3xflag (×400 magnification). (M and N) (M) The apoptosis of vehicle or TGF-β1-stimulated LX-2 cells transducted with LV-empty or LV-4EBP1-4A-3xflag determined using flow cytometry and (N) percentages of apoptotic cells (early and late apoptotic cells). EV, LV-empty; OE, LV-4EBP1-4A-3xflag. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HIF-1α, hypoxia inducible factor 1 subunit alpha; LV, lentivirus; PI, propidium iodide; RT-qPCR, quantitative reverse transcription polymerase chain reaction; TGF-β1, transforming growth factor beta 1. Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00013-4-40752108-figure-6.jpgAnti-HIF-1-alpha Rabbit Monoclonal Antibody(H) The protein expression of α-SMA, COL1α1, vimentin, fibronectin, E-cadherin, and HIF-1α in LX-2 cells was analyzed using western blotting. (I) Immunofluorescence double staining of α-SMA and HIF-1α in TGF-β1-stimulated and DMSO or AZD8055-treated LX-2 cells transducted with LV-control-shRNA or LV-4EBP1-shRNA (×400 magnification). (L and M) (L) The apoptosis of LX-2 cells determined using flow cytometry and (M) percentages of apoptotic cells (early and late apoptotic cells). NC, LV-control-shRNA; KD, LV-4EBP1-shRNA. Values are the mean ± SD (unpaired two-sample Student’s t test). ∗∗p < 0.01, ∗∗∗p < 0.001, and ∗∗∗∗p < 0.0001; ns, not significant. α-SMA, alpha-smooth muscle actin; DAPI, 4′,6-diamidino-2-phenylindole; GAPDH, glyceraldehyde-3-phosphate dehydrogenase; HIF-1α, hypoxia inducible factor 1 subunit alpha; LV, lentivirus; PI, propidium iodide; TGF-β1, transforming growth factor beta 1. Index in iScience under a CC BY license. DOI: <a href='https://www.cell.com/iscience/fulltext/S2589-0042(25)01673-6'>10.1016/j.isci.2025.113412</a> https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-delta-2-catenin-rabbit-monoclonal-antibody-m04447-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04447-wb.jpgAnti-delta 2 Catenin Rabbit Monoclonal AntibodyWestern blot analysis of delta 2 Catenin expression in Mouse brain cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04447-wb7.jpgAnti-delta 2 Catenin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-acetyl-k36-rabbit-monoclonal-antibody-m12477-19-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-19-wb.jpgAnti-Histone H3 (acetyl K36) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (acetyl K36) expression in HeLa treated with Sodium butyrate cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-19-wb7.jpgAnti-Histone H3 (acetyl K36) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-19-wb8.jpgAnti-Histone H3 (acetyl K36) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkc-rabbit-monoclonal-antibody-m00743-2-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-2-wb7.jpgAnti-PKC-gamma Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-2-wb.jpgAnti-PKC-gamma Rabbit Monoclonal AntibodyWestern blot analysis of PKC expression in (1) HeLa cell lysate; (2) A431 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-2-wb8.jpgAnti-PKC-gamma Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-2-ip7.jpgAnti-PKC-gamma Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-2-wb9.jpgAnti-PKC-gamma Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-methyl-k79-rabbit-monoclonal-antibody-m12477-20-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-20-wb.jpgAnti-Histone H3 (mono methyl K79) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (mono methyl K79) expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-20-wb9.jpgAnti-Histone H3 (mono methyl K79) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-20-wb7.jpgAnti-Histone H3 (mono methyl K79) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-20-wb8.jpgAnti-Histone H3 (mono methyl K79) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-caspase-6-rabbit-monoclonal-antibody-m02631-4-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb7.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb10.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb8.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb11.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb9.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb12.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyWestern blot analysis of Caspase-6 expression in (1) Mouse spleen lysate; (2) Rat kidney cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb13.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02631-4-wb14.jpgAnti-Caspase-6 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2b-formyl-k116-rabbit-monoclonal-antibody-m07286-5-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-5-wb.jpgAnti-Histone H2B (formyl K116) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2B (formyl K116) expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-5-wb7.jpgAnti-Histone H2B (formyl K116) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-5-wb8.jpgAnti-Histone H2B (formyl K116) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-cdk2-t160-cdk1-t161-rabbit-monoclonal-antibody-m00209t160t161-boster.html2026-03-17T05:15:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209t160t161-p-cdk1-2-primary-antibodies-wb-testing-1_1.jpgAnti-Phospho-CDK2(T160)+CDK1(T161) Rabbit Monoclonal AntibodyFigure 1. Western blot analysis of CDK2(Phospho-T160)/CDK1(Phospho-T161) using anti-CDK2(Phospho-T160)/CDK1(Phospho-T161) antibody (M00209T160T161). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: human K562 whole cell lysates, Lane 6: human PC-3 whole cell lysates, Lane 7: human U251 whole cell lysates, Lane 8: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDK2(Phospho-T160)/CDK1(Phospho-T161) antigen affinity purified monoclonal antibody (M00209T160T161) at a dilution of 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CDK2(Phospho-T160)/CDK1(Phospho-T161) at approximately 32-34 kDa. The expected band size for CDK2(Phospho-T160)/CDK1(Phospho-T161) is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209t160t161-p-cdk1-2-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-CDK2(T160)+CDK1(T161) Rabbit Monoclonal AntibodyFigure 2. IHC analysis of CDK2(Phospho-T160)/CDK1(Phospho-T161) using anti-CDK2(Phospho-T160)/CDK1(Phospho-T161) antibody (M00209T160T161). CDK2(Phospho-T160)/CDK1(Phospho-T161) was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK2(Phospho-T160)/CDK1(Phospho-T161) Antibody (M00209T160T161) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00209t160t161-p-cdk1-2-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-CDK2(T160)+CDK1(T161) Rabbit Monoclonal AntibodyFigure 3. IHC analysis of CDK2(Phospho-T160)/CDK1(Phospho-T161) using anti-CDK2(Phospho-T160)/CDK1(Phospho-T161) antibody (M00209T160T161). CDK2(Phospho-T160)/CDK1(Phospho-T161) was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-CDK2(Phospho-T160)/CDK1(Phospho-T161) Antibody (M00209T160T161) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h2b-acetyl-k16-rabbit-monoclonal-antibody-m07286-6-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-6-wb.jpgAnti-Histone H2B (acetyl K16) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H2B (acetyl K16) expression in HeLa treated with Trichostatin A cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-6-wb9.jpgAnti-Histone H2B (acetyl K16) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-6-wb7.jpgAnti-Histone H2B (acetyl K16) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-6-wb8.jpgAnti-Histone H2B (acetyl K16) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ppar-gamma-rabbit-monoclonal-antibody-m00449-2-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00449-2-wb.jpgAnti-PPAR gamma Rabbit Monoclonal AntibodyWestern blot analysis of PPAR gamma expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00449-2-fgene-16-1529797-g001.jpgAnti-PPAR gamma Rabbit Monoclonal AntibodyH19 and PPARγ are upregulated in the femoral head and BMSCs of patients with SONFH. (A, B) X-ray photo and pathological structure of the femoral head from an ARCO stage V SONFH patient. The images show alterations in the morphology of the femoral head, characterized by collapse and flattening, as well as radiographic signs indicative of hip osteoarthritis. (C) Morphology of BMSCs from a patient with SONFH. (D, E) Expression levels of H19 and PPARγ in the femoral head and BMSCs from a patient with SONFH. All experimental procedures were performed in triplicate with internal normalization to GAPDH expression levels. The relative expression levels of each gene were analyzed using the 2 −△△Ct method (n = 8, all data are shown as the mean ± SD of three independent experiments, *p < 0.05, **p < 0.01). Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2025.1529797/full'>40259926</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00449-2-fgene-16-1529797-g002.jpgAnti-PPAR gamma Rabbit Monoclonal AntibodyH19 participates in increased adipogenesis of BMSCs and positively regulates PPARγ expression in SONFH. (A) Expression level of H19 in BMSCs after transfection with sh-H19. (B) Oil Red O staining (200×) of BMSCs after transfection with sh-H19. (C, D) Quantification of Oil Red O staining (200×) of BMSCs after transfection with sh-H19. (E, F) The expression of fatty acid-binding protein 4 (FABP4) was detected by qRT-PCR and Western blot after knocking-down of H19. (G) The expression levels of H19 and PPARγ 1 week following the knockdown of H19. (n = 3, all data are shown as the mean ± SD of three independent experiments, *p < 0.05, **p < 0.01). Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2025.1529797/full'>40259926</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00449-2-fgene-16-1529797-g003.jpgAnti-PPAR gamma Rabbit Monoclonal AntibodyH19 modulates PPARγ expression through miR-130b-3p. (A) Three databases, StarBase, DIANA tools, and miRWalk, were used to predict candidate micro (mi)RNAs as shown in the Venn diagram. (B) Expression levels of three candidate miRNAs (miR-301b-3p, miR-130b-3p, and miR-130a-3p) after knockdown of H19. (C) The binding sites of miR-130b-3p with H19 and PPARγ. (D) Effect of miR-130b-3p on the luciferase activity of wild-type (WT)-H19 and mutant (MT)-H19 reporter systems. (E) Effect of miR-130b-3p on the luciferase activity of WT-FABP4 and MT-FABP4 reporter systems was detected via luciferase reporter assay. (F, G) The expression of PPARγ is significantly decreased upon knocking down H19. This reduction could be reversed through co-transfection with a miR-130b-3p inhibitor. (H, I) The expression of PPARγ was significantly augmented when H19 was upregulated. This elevation in PPARγ expression could be counteracted by co-transfecting with a miR-130b-3p mimic. (n = 3, all data are shown as the mean ± SD of three independent experiments, **p < 0.01, ***p < 0.001). Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/journals/genetics/articles/10.3389/fgene.2025.1529797/full'>40259926</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00449-2-wb7.jpgAnti-PPAR gamma Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-mono-methyl-k14-rabbit-monoclonal-antibody-m12477-21-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-21-wb.jpgAnti-Histone H3 (mono methyl K14) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (mono methyl K14) expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-21-wb7.jpgAnti-Histone H3 (mono methyl K14) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-21-wb8.jpgAnti-Histone H3 (mono methyl K14) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-di-methyl-k4-rabbit-monoclonal-antibody-m12477-22-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-22-wb.jpgAnti-Histone H3 (di methyl K4) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (di methyl K4) expression in HeLa cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-22-wb7.jpgAnti-Histone H3 (di methyl K4) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-22-wb8.jpgAnti-Histone H3 (di methyl K4) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pkc-alpha-t497-rabbit-monoclonal-antibody-m00497t497-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00497t497-wb.jpgAnti-Phospho-PKC alpha (T497) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-PKC alpha (T497) expression in HeLa treated with Calyculin A cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00497t497-wb9.jpgAnti-Phospho-PKC alpha (T497) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00497t497-wb7.jpgAnti-Phospho-PKC alpha (T497) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00497t497-wb8.jpgAnti-Phospho-PKC alpha (T497) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-src-y529-rabbit-monoclonal-antibody-m00107y529-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107y529-wb.jpgAnti-Phospho-Src (Y529) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-Src (Y529) expression in A431 cell treated with EGF lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107y529-wb7.jpgAnti-Phospho-Src (Y529) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00107y529-wb8.jpgAnti-Phospho-Src (Y529) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-tri-methyl-k27-rabbit-monoclonal-antibody-m12477-23-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01762-1-nme2-primary-antibodies-wb-testing-1_1.jpgAnti-Histone H3 (tri methyl K27) Rabbit Monoclonal AntibodyWestern blot analysis of NME2 using anti-NME2 antibody (M01762-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human LNCAP whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NME2 antigen affinity purified monoclonal antibody (M01762-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NME2 at approximately 15 kDa. The expected band size for NME2 is at 15 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-bcar1-y410-rabbit-monoclonal-antibody-m00960y410-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00960y410-wb.jpgAnti-Phospho-BCAR1 (Y410) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-BCAR1 (Y410) expression in HeLa treated with pervanadate cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-p70-s6-kinase-beta-s371-rabbit-monoclonal-antibody-m05845s371-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05845s371-wb.jpgAnti-Phospho-P70 S6 Kinase beta (S371) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-P70 S6 Kinase beta (S371) expression in 293 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05845s371-wb7.jpgAnti-Phospho-P70 S6 Kinase beta (S371) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05845s371-wb8.jpgAnti-Phospho-P70 S6 Kinase beta (S371) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-phospholipase-c-gamma-1-plc-gamma-1-y1253-rabbit-monoclonal-antibody-m00677y1253-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00677y1253-wb.jpgAnti-phospho-Phospholipase C gamma 1/PLC-gamma-1 (Y1253) Rabbit Monoclonal AntibodyWestern blot analysis of phospho-Phospholipase C gamma 1/PLC-gamma-1 (Y1253) expression in Jurkat treated with Pervanadate lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-acetyl-coenzyme-a-carboxylase-rabbit-monoclonal-antibody-m01802-2-boster.html2026-03-17T05:15:55+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-frg1-rabbit-monoclonal-antibody-m04940-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04940-wb7.jpgAnti-FRG1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04940-wb8.jpgAnti-FRG1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-crkl-y207-rabbit-monoclonal-antibody-m02100y207-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100y207-wb7.jpgAnti-Phospho-CrkL (Y207) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100y207-wb8.jpgAnti-Phospho-CrkL (Y207) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100y207-wb9.jpgAnti-Phospho-CrkL (Y207) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-histone-h3-s28-rabbit-monoclonal-antibody-m12477s28-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477s28-wb7.jpgAnti-Phospho-Histone H3 (S28) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-crmp2-t514-rabbit-monoclonal-antibody-m02860t514-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02860t514-wb7.jpgAnti-Phospho-CRMP2 (T514) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02860t514-wb8.jpgAnti-Phospho-CRMP2 (T514) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02860t514-wb9.jpgAnti-Phospho-CRMP2 (T514) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-syk-y323-rabbit-monoclonal-antibody-m00490y323-boster.html2026-03-17T05:15:55+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-acbd3-rabbit-monoclonal-antibody-m05645-1-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05645-1-wb7.jpgAnti-ACBD3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myeloperoxidase-rabbit-monoclonal-antibody-m00372-2-boster.html2026-03-17T05:15:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00372-2-wb7.jpgAnti-Myeloperoxidase Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd163-rabbit-monoclonal-antibody-m00812-4-boster.html2026-03-17T05:15:55+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-cd163-rabbit-monoclonal-antibody-m00812-5-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00812-5-wb.jpgAnti-CD163 Rabbit Monoclonal AntibodyWestern blot analysis of CD163 expression in Human fetal liver cell lysate. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-icam1-cd54-rabbit-monoclonal-antibody-m00171-5-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-5-icam1-primary-antibodies-wb-testing-1.jpgAnti-ICAM1 / CD54 Rabbit Monoclonal AntibodyWestern blot analysis of ICAM1 using anti-ICAM1 antibody (M00171-5). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse liver tissue lysates, Lane 2: mouse spleen tissue lysates, Lane 3: mouse kidney tissue lysates, Lane 4: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ICAM1 antigen affinity purified monoclonal antibody (M00171-5) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ICAM1 at approximately 100 kDa. The expected band size for ICAM1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-5-icam1-primary-antibodies-ihc-testing-3.jpgAnti-ICAM1 / CD54 Rabbit Monoclonal AntibodyIHC analysis of ICAM1 using anti-ICAM1 antibody (M00171-5). ICAM1 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ICAM1 Antibody (M00171-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-5-icam1-primary-antibodies-ihc-testing-2.jpgAnti-ICAM1 / CD54 Rabbit Monoclonal AntibodyIHC analysis of ICAM1 using anti-ICAM1 antibody (M00171-5). ICAM1 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ICAM1 Antibody (M00171-5) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sypl1-rabbit-monoclonal-antibody-m12424-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12424-wb7.jpgAnti-SYPL1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-usp5-rabbit-monoclonal-antibody-m04550-3-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04550-3-wb7.jpgAnti-USP5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04550-3-wb10.jpgAnti-USP5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04550-3-wb8.jpgAnti-USP5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04550-3-wb.jpgAnti-USP5 Rabbit Monoclonal AntibodyWestern blot analysis of USP5 expression in MCF-7 cell lysate.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04550-3-wb9.jpgAnti-USP5 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-rac3-rabbit-monoclonal-antibody-m03252-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03252-wb7.jpgAnti-RAC3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03252-wb8.jpgAnti-RAC3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ubf1-rabbit-monoclonal-antibody-m05134-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05134-wb7.jpgAnti-UBF1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05134-wb8.jpgAnti-UBF1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ubf1-s484-rabbit-monoclonal-antibody-m05134s484-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05134s484-wb7.jpgAnti-Phospho-UBF1 (S484) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05134s484-wb8.jpgAnti-Phospho-UBF1 (S484) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-acetyl-k9-rabbit-monoclonal-antibody-m12477-24-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-24-histone-h3-primary-antibodies-wb-testing-1.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal AntibodyFigure 1. Western blot analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-24). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H3 (acetyl K9) antigen affinity purified monoclonal antibody (M12477-24) at a dilution of 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H3 (acetyl K9) at approximately 17 kDa. The expected band size for Histone H3 (acetyl K9) is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-24-histone-h3-primary-antibodies-ihc-testing-2.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal AntibodyFigure 2. IHC analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-24). Histone H3 (acetyl K9) was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K9) Antibody (M12477-24) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-24-histone-h3-primary-antibodies-ihc-testing-3.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal AntibodyFigure 3. IHC analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-24). Histone H3 (acetyl K9) was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Histone H3 (acetyl K9) Antibody (M12477-24) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-histone-h3-acetyl-k9-rabbit-monoclonal-antibody-m12477-25-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-histone-h3-primary-antibodies-wb-testing-1.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal Antibody Western blot analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-25). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human T98G whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: human K562 whole cell lysates, Lane 6: human SH-SY5Y whole cell lysates, Lane 7: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Histone H3 (acetyl K9) antigen affinity purified monoclonal antibody (M12477-25) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Histone H3 (acetyl K9) at approximately 15 kDa. The expected band size for Histone H3 (acetyl K9) is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-wb7_1.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-wb8_1.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-wb_1.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal AntibodyWestern blot analysis of Histone H3 (acetyl K9) expression in C6 cell lysate treated with Trichostatin A.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-histone_h3-primary-antibodies-ihc-testing-2.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-25). Histone H3 (acetyl K9) was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 (acetyl K9) Antibody (M12477-25) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-histone_h3-primary-antibodies-ihc-testing-3.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-25). Histone H3 (acetyl K9) was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 (acetyl K9) Antibody (M12477-25) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-histone_h3-primary-antibodies-ihc-testing-4.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-25). Histone H3 (acetyl K9) was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 (acetyl K9) Antibody (M12477-25) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-histone_h3-primary-antibodies-ihc-testing-5.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-25). Histone H3 (acetyl K9) was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 (acetyl K9) Antibody (M12477-25) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-25-histone_h3-primary-antibodies-ihc-testing-6.jpgAnti-Histone H3 (acetyl K9) Rabbit Monoclonal Antibody IHC analysis of Histone H3 (acetyl K9) using anti-Histone H3 (acetyl K9) antibody (M12477-25). Histone H3 (acetyl K9) was detected in a paraffin-embedded section of human breast tissue tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Histone H3 (acetyl K9) Antibody (M12477-25) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erp27-rabbit-monoclonal-antibody-m12307-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12307-wb7.jpgAnti-ERP27 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sdhb-rabbit-monoclonal-antibody-m01090-4-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01090-4-wb7.jpgAnti-SDHB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01090-4-ip7.jpgAnti-SDHB Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01090-4-wb8.jpgAnti-SDHB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01090-4-wb9.jpgAnti-SDHB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-sdhc-rabbit-monoclonal-antibody-m02725-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02725-wb7.jpgAnti-SDHC Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02725-wb8.jpgAnti-SDHC Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:6K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pkc-delta-y311-rabbit-monoclonal-antibody-m00822y311-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00822y311-wb7.jpgAnti-Phospho-PKC delta (Y311) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkc-rabbit-monoclonal-antibody-m00743-3-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-3-wb7.jpgAnti-PKC Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-3-wb8.jpgAnti-PKC Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-3-wb9.jpgAnti-PKC Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-vapa-rabbit-monoclonal-antibody-m05329-2-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05329-2-wb7.jpgAnti-VAPA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05329-2-wb8.jpgAnti-VAPA Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-picalm-rabbit-monoclonal-antibody-m02053-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02053-wb7.jpgAnti-PICALM Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-acadvl-vlcad-rabbit-monoclonal-antibody-m02607-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02607-wb7.jpgAnti-ACADVL/VLCAD Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02607-wb8.jpgAnti-ACADVL/VLCAD Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-ribophorin-i-rabbit-monoclonal-antibody-m05063-1-boster.html2026-03-17T05:15:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05063-1-wb7.jpgAnti-Ribophorin I Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05063-1-wb8.jpgAnti-Ribophorin I Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ctnnd1-y228-rabbit-monoclonal-antibody-m02333y228-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02333y228-phospho-ctnnd1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-CTNND1 (Y228) Rabbit Monoclonal AntibodyWestern blot analysis of Phospho-CTNND1 using anti-Phospho-CTNND1 antibody (M02333Y228). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 μg of sample under reducing conditions. Lane 1: A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phospho-CTNND1 antigen affinity purified monoclonal antibody (M02333Y228) at 0.5 μg/ml overnight at 4°C, then washed with TBS-0.1%Tween-20 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. The expected band size for ANO1 is at 108 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-glut4-s488-rabbit-monoclonal-antibody-m00528s488-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00528s488-wb7.jpgAnti-Phospho-GLUT4 (S488) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00528s488-wb8.jpgAnti-Phospho-GLUT4 (S488) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tuberin-t1462-rabbit-monoclonal-antibody-m00229t1462-boster.html2026-03-17T05:15:57+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-map2-s136-rabbit-monoclonal-antibody-m01201s136-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01201s136-wb7.jpgAnti-Phospho-MAP2 (S136) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-syvn1-hrd1-rabbit-monoclonal-antibody-m02670-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02670-syvn1-primary-antibodies-wb-testing-1.jpgAnti-SYVN1 / HRD1 Rabbit Monoclonal AntibodyWestern blot analysis of HRD1/SYVN1 using anti-HRD1/SYVN1 antibody (M02670). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HRD1/SYVN1 antigen affinity purified monoclonal antibody (M02670) at 1: 500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HRD1/SYVN1 at approximately 65 kDa. The expected band size for HRD1/SYVN1 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02670-syvn1-primary-antibodies-ihc-testing-1.jpgAnti-SYVN1 / HRD1 Rabbit Monoclonal AntibodyIHC analysis of HRD1/SYVN1 using anti-HRD1/SYVN1 antibody (M02670). HRD1/SYVN1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 50 rabbit anti-HRD1/SYVN1 Antibody (M02670) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02670-ip7.jpgAnti-SYVN1 / HRD1 Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution) https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-lyn-rabbit-monoclonal-antibody-m01424-1-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01424-1-wb7.jpgAnti-Lyn Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01424-1-wb8.jpgAnti-Lyn Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ampa-receptor-1-s831-rabbit-monoclonal-antibody-m02677s831-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02677s831-wb7.jpgAnti-Phospho-AMPA Receptor 1 (S831) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02677s831-wb8.jpgAnti-Phospho-AMPA Receptor 1 (S831) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pka-c-thr197-rabbit-monoclonal-antibody-m00743t197-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743t197-wb7.jpgAnti-Phospho-PKA C (Thr197) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743t197-p-prkacg-primary-antibodies-wb-testing-1.jpgAnti-Phospho-PKA C (Thr197) Rabbit Monoclonal AntibodyWestern blot analysis of P-PRKACG using anti-P-PRKACG antibody (M00743T197). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-PRKACG antigen affinity purified monoclonal antibody (M00743T197) at 1:500 overnight at 4°C, then washed with TBS-10%%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-PRKACG at approximately 38 kDa. The expected band size for P-PRKACG is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743t197-wb.jpgAnti-Phospho-PKA C (Thr197) Rabbit Monoclonal AntibodyWestern blot analysis of extracts from HeLa cells, using ADCY1 antibody. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-snap25-rabbit-monoclonal-antibody-m01625-3-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01625-3-wb7.jpgAnti-SNAP25 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-vasp-s156-rabbit-monoclonal-antibody-m00303s156-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00303s156-wb7.jpgAnti-Phospho-VASP (S156) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-c-reactive-protein-rabbit-monoclonal-antibody-m00249-2-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00249-2-wb7.jpgAnti-C Reactive Protein Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00249-2-wb8.jpgAnti-C Reactive Protein Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-integrin-beta-7-rabbit-monoclonal-antibody-m05433-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05433-wb7.jpgAnti-Integrin beta 7 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05433-itgb7-primary-antibodies-ihc-testing-4.jpgAnti-Integrin beta 7 Rabbit Monoclonal AntibodyIHC analysis of ITGB7 using anti-ITGB7 antibody (M05433). ITGB7 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGB7 Antibody (M05433) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05433-itgb7-primary-antibodies-ihc-testing-3.jpgAnti-Integrin beta 7 Rabbit Monoclonal AntibodyIHC analysis of ITGB7 using anti-ITGB7 antibody (M05433). ITGB7 was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGB7 Antibody (M05433) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05433-itgb7-primary-antibodies-ihc-testing-1.jpgAnti-Integrin beta 7 Rabbit Monoclonal AntibodyIHC analysis of ITGB7 using anti-ITGB7 antibody (M05433). ITGB7 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGB7 Antibody (M05433) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05433-itgb7-primary-antibodies-ihc-testing-2.jpgAnti-Integrin beta 7 Rabbit Monoclonal AntibodyIHC analysis of ITGB7 using anti-ITGB7 antibody (M05433). ITGB7 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-ITGB7 Antibody (M05433) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-fak-y576-y577-rabbit-monoclonal-antibody-m00151y576y577-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00151y576y577-wb7.jpgAnti-Phospho-FAK (Y576 + Y577) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-mst1-mst2-t183-t180-rabbit-monoclonal-antibody-m02224t183t180-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02224t183t180-wb7.jpgAnti-Phospho-MST1/MST2 (T183 + T180) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02224t183t180-wb8.jpgAnti-Phospho-MST1/MST2 (T183 + T180) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-eif4ebp1-t70-rabbit-monoclonal-antibody-m00968t70-boster.html2026-03-17T05:15:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00968t70-p-eif4ebp1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-eIF4EBP1 (T70) Rabbit Monoclonal AntibodyWestern blot analysis of P-EIF4EBP1 using anti-P-EIF4EBP1 antibody (M00968T70). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-EIF4EBP1 antigen affinity purified monoclonal antibody (M00968T70) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-EIF4EBP1 at approximately 17 kDa. The expected band size for P-EIF4EBP1 is at 17 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-caveolin-1-y14-rabbit-monoclonal-antibody-m00179y14-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-phospho-pkr-t45-rabbit-monoclonal-antibody-m01384t451-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pdgfr-beta-y1009-rabbit-monoclonal-antibody-m00096y1009-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-eif4ebp1-2-3-t46-t46-t32-rabbit-monoclonal-antibody-m00968t46t32-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00968t46t32-p-4ebp1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-eIF4EBP1/2/3 (T46+T46+T32) Rabbit Monoclonal Antibody Western blot analysis of 4EBP1/EIF4EBP1/2/3(Phospho-T46/T46/T32) using anti-4EBP1/EIF4EBP1/2/3(Phospho-T46/T46/T32) antibody (M00968T46T32). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-4EBP1/EIF4EBP1/2/3(Phospho-T46/T46/T32) antigen affinity purified monoclonal antibody (M00968T46T32) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for 4EBP1/EIF4EBP1/2/3(Phospho-T46/T46/T32) at approximately 18 kDa. The expected band size for 4EBP1/EIF4EBP1/2/3(Phospho-T46/T46/T32) is at 18 kDa. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tau-s356-rabbit-monoclonal-antibody-m00097s356-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pleiotrophin-rabbit-monoclonal-antibody-m01368-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01368-wb7.jpgAnti-Pleiotrophin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01368-ptn-primary-antibodies-ihc-testing-1.jpgAnti-Pleiotrophin Rabbit Monoclonal AntibodyIHC analysis of PTN using anti-PTN antibody (M01368). PTN was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PTN Antibody (M01368) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01368-ptn-primary-antibodies-ihc-testing-2.jpgAnti-Pleiotrophin Rabbit Monoclonal AntibodyIHC analysis of PTN using anti-PTN antibody (M01368). PTN was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PTN Antibody (M01368) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01368-wb8.jpgAnti-Pleiotrophin Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-phospholamban-s16-rabbit-monoclonal-antibody-m01395s16-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01395s16-wb7.jpgAnti-Phospho-Phospholamban (S16) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01395s16-wb8.jpgAnti-Phospho-Phospholamban (S16) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-ikb-alpha-y42-rabbit-monoclonal-antibody-m01139y42-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-plcb3-s537-rabbit-monoclonal-antibody-m04226s537-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04226s537-wb7.jpgAnti-Phospho-PLCB3 (S537) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-protein-kinase-d2-s876-rabbit-monoclonal-antibody-m04056s876-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pdgf-receptor-beta-cd140b-y1021-rabbit-monoclonal-antibody-m00096y1021-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-beta-arrestin-1-s412-rabbit-monoclonal-antibody-m02185s412-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02185s412-wb7.jpgAnti-Phospho-beta Arrestin 1 (S412) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02185s412-wb8.jpgAnti-Phospho-beta Arrestin 1 (S412) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-grb2-rabbit-monoclonal-antibody-m00351-2-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00351-2-wb7.jpgAnti-GRB2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00351-2-wb8.jpgAnti-GRB2 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-rsk1-p90-t573-rabbit-monoclonal-antibody-m01058t573-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-crkl-rabbit-monoclonal-antibody-m02100-2-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100-2-crkl-primary-antibodies-wb-testing-1.jpgAnti-CrkL Rabbit Monoclonal AntibodyWestern blot analysis of CRKL using anti-CRKL antibody (M02100-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Raji whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse spleen tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CRKL antigen affinity purified monoclonal antibody (M02100-2) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CRKL at approximately 37 kDa. The expected band size for CRKL is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100-2-crkl-primary-antibodies-ihc-testing-1.jpgAnti-CrkL Rabbit Monoclonal AntibodyIHC analysis of CRKL using anti-CRKL antibody (M02100-2). CRKL was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CRKL Antibody (M02100-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100-2-crkl-primary-antibodies-ihc-testing-2.jpgAnti-CrkL Rabbit Monoclonal AntibodyIHC analysis of CRKL using anti-CRKL antibody (M02100-2). CRKL was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CRKL Antibody (M02100-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100-2-crkl-primary-antibodies-ihc-testing-3.jpgAnti-CrkL Rabbit Monoclonal AntibodyIHC analysis of CRKL using anti-CRKL antibody (M02100-2). CRKL was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CRKL Antibody (M02100-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100-2-crkl-primary-antibodies-ihc-testing-4.jpgAnti-CrkL Rabbit Monoclonal AntibodyIHC analysis of CRKL using anti-CRKL antibody (M02100-2). CRKL was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-CRKL Antibody (M02100-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02100-2-ip7.jpgAnti-CrkL Rabbit Monoclonal AntibodyImmunoprecipitate (IP) analysis using the Antibody at 1:50 dilution. (wb at 1:1K dilution) https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-erbb-3-y1289-rabbit-monoclonal-antibody-m00539y1289-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-alpha-synuclein-y125-rabbit-monoclonal-antibody-m00215y125-boster.html2026-03-17T05:15:58+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-chk2-s33-s35-rabbit-monoclonal-antibody-m00277s33s35-boster.html2026-03-17T05:15:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00277s33s35-wb7.jpgAnti-Phospho-Chk2 (S33 + S35) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1k dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-myh2-rabbit-monoclonal-antibody-m05048-boster.html2026-03-17T05:15:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pras40-t246-rabbit-monoclonal-antibody-m03629t246-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03629t246-wb7.jpgAnti-Phospho-PRAS40 (T246) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03629t246-wb8.jpgAnti-Phospho-PRAS40 (T246) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03629t246-wb9.jpgAnti-Phospho-PRAS40 (T246) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-beta-catenin-t41-s45-rabbit-monoclonal-antibody-m00004t41s45-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004t41s45-wb7.jpgAnti-Phospho-beta Catenin (T41 + S45) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00004t41s45-wb8.jpgAnti-Phospho-beta Catenin (T41 + S45) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-tuberin-s939-rabbit-monoclonal-antibody-m00229s939-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229s939-p-tuberin-primary-antibodies-wb-testing-1_1.jpgAnti-Phospho-Tuberin (S939) Rabbit Monoclonal AntibodyFigure 1. Western blot analysis of Tuberin/TSC2 (Phospho-S939) using anti-Tuberin/TSC2 (Phospho-S939) antibody (M00229S939). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tuberin/TSC2 (Phospho-S939) antigen affinity purified monoclonal antibody (M00229S939) at a dilution of 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Tuberin/TSC2 (Phospho-S939) at approximately 240 kDa. The expected band size for Tuberin/TSC2 (Phospho-S939) is at 201 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229s939-p-tsc2-primary-antibodies-wb-testing-2_1.jpgAnti-Phospho-Tuberin (S939) Rabbit Monoclonal AntibodyWestern blot analysis of Tuberin/TSC2 using anti-Tuberin/TSC2 antibody (M00229S939). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tuberin/TSC2 antigen affinity purified monoclonal antibody (M00229S939) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Tuberin/TSC2 at approximately 240 kDa. The expected band size for Tuberin/TSC2 is at 201 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229s939-p-tsc2-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-Tuberin (S939) Rabbit Monoclonal AntibodyIHC analysis of Tuberin/TSC2 using anti-Tuberin/TSC2 antibody (M00229S939). Tuberin/TSC2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Tuberin/TSC2 Antibody (M00229S939) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229s939-p-tuberin-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-Tuberin (S939) Rabbit Monoclonal AntibodyFigure 2. IHC analysis of Tuberin/TSC2 (Phospho-S939) using anti-Tuberin/TSC2 (Phospho-S939) antibody (M00229S939). Tuberin/TSC2 (Phospho-S939) was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Tuberin/TSC2 (Phospho-S939) Antibody (M00229S939) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229s939-p-tuberin-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-Tuberin (S939) Rabbit Monoclonal AntibodyFigure 3. IHC analysis of Tuberin/TSC2 (Phospho-S939) using anti-Tuberin/TSC2 (Phospho-S939) antibody (M00229S939). Tuberin/TSC2 (Phospho-S939) was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with a dilution of 1:50 rabbit anti-Tuberin/TSC2 (Phospho-S939) Antibody (M00229S939) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00229s939-p-tsc2-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-Tuberin (S939) Rabbit Monoclonal AntibodyIHC analysis of Tuberin/TSC2 using anti-Tuberin/TSC2 antibody (M00229S939). Tuberin/TSC2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-Tuberin/TSC2 Antibody (M00229S939) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-nucleophosmin-s125-rabbit-monoclonal-antibody-m00450s125-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-wb-testing-1.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyWestern blot analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human SH-SY5Y whole cell lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P-NPM1 antigen affinity purified monoclonal antibody (M00450S125) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for P-NPM1 at approximately 38 kDa. The expected band size for P-NPM1 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-1.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-2.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-3.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-4.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-5.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-6.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-7.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-8.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-9.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-10.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-11.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00450s125-p-npm1-primary-antibodies-ihc-testing-12.jpgAnti-Phospho-Nucleophosmin (S125) Rabbit Monoclonal AntibodyIHC analysis of P-NPM1 using anti-P-NPM1 antibody (M00450S125). P-NPM1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-P-NPM1 Antibody (M00450S125) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-tim50-rabbit-monoclonal-antibody-m10056-2-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10056-2-wb7.jpgAnti-TIM50 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10056-2-wb8.jpgAnti-TIM50 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10056-2-wb9.jpgAnti-TIM50 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-osteocalcin-rabbit-monoclonal-antibody-m03269-1-boster.html2026-03-17T05:15:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pkc-delta-t507-rabbit-monoclonal-antibody-m00743t507-boster.html2026-03-17T05:15:59+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-phospho-pkc-s729-rabbit-monoclonal-antibody-m00743s729-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743s729-wb7.jpgAnti-Phospho-PKC (S729) Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/catalog/product/view/id/1259012026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-4-wb7.jpgAnti-PKC Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-4-wb8.jpgAnti-PKC Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-pkc-rabbit-monoclonal-antibody-m00743-5-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-5-wb7.jpgAnti-PKC-beta Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-5-wb8.jpgAnti-PKC-beta Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00743-5-wb9.jpgAnti-PKC-beta Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:5K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mrpl11-rabbit-monoclonal-antibody-m11059-2-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11059-2-wb7.jpgAnti-MRPL11 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-erp72-rabbit-monoclonal-antibody-m07267-4-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07267-4-wb7.jpgAnti-ERp72 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:1W dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-nelfb-rabbit-monoclonal-antibody-m31150-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31150-wb7.jpgAnti-NELFB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31150-wb8.jpgAnti-NELFB Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:3K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-btf-rabbit-monoclonal-antibody-m04100-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04100-wb7.jpgAnti-BTF Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-mtor-rabbit-monoclonal-antibody-m00003-3-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00003-3-wb7.jpgAnti-mTOR Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:500 dilution for 1 hour at room temperature. https://www.bosterbio.com/products/primary-antibodies/recombinant-antibodies/anti-klc3-rabbit-monoclonal-antibody-m09860-boster.html2026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09860-wb7.jpgAnti-KLC3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09860-wb8.jpgAnti-KLC3 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2W dilution for 1 hour at room temperature. https://www.bosterbio.com/catalog/product/view/id/1259092026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00722-1-wb7.jpgAnti-ROCK1 Rabbit Monoclonal AntibodyAll lanes use the Antibody at 1:2K dilution for 1 hour at room temperature. https://www.bosterbio.com/catalog/product/view/id/1259102026-03-17T05:15:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13516-dcaf13-primary-antibodies-wb-testing-1.jpgAnti-DCAF13 Rabbit Monoclonal Antibody Western blot analysis of DCAF13 using anti-DCAF13 antibody (M13516). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whoel cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DCAF13 antigen affinity purified monoclonal antibody (M13516) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:500 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DCAF13 at approximately 48 kDa. The expected band size for DCAF13 is at 51 kDa. https://www.bosterbio.com/catalog/product/view/id/1259112026-03-25T05:24:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2278.pngHuman MEGF9 ELISA Kit PicoKine®Human MEGF9 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1259122026-03-10T04:37:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2279.pngHuman MEPE ELISA Kit PicoKine®Human MEPE PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1259132026-03-10T04:37:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2280.jpgHuman MD2 ELISA Kit PicoKine®Human MD2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1259212026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03602-2-slc7a7-primary-antibodies-wb-testing-1.jpgAnti-SLC7A7 Antibody Picoband® Western blot analysis of SLC7A7 using anti-SLC7A7 antibody (A03602-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLC7A7 antigen affinity purified polyclonal antibody (Catalog # A03602-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLC7A7 at approximately 60 kDa. The expected band size for SLC7A7 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03602-2-slc7a7-primary-antibodies-ihc-testing-2.jpgAnti-SLC7A7 Antibody Picoband® IHC analysis of SLC7A7 using anti-SLC7A7 antibody (A03602-2). SLC7A7 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC7A7 Antibody (A03602-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03602-2-slc7a7-primary-antibodies-ihc-testing-3.jpgAnti-SLC7A7 Antibody Picoband® IHC analysis of SLC7A7 using anti-SLC7A7 antibody (A03602-2). SLC7A7 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLC7A7 Antibody (A03602-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03602-2-slc7a7-primary-antibodies-if-testing-4.jpgAnti-SLC7A7 Antibody Picoband® IF analysis of SLC7A7 using anti-SLC7A7 antibody (A03602-2). SLC7A7 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-SLC7A7 Antibody (A03602-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/primary-antibodies/anti-african-malaria-mosquito-spz3-dz41444-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-oryzias-latipes-keratin-type-i-cytoskeletal-13-dz41497-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-zebrafish-otpa-dz41502-boster.html2026-03-17T05:16:00+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-zebrafish-opta-dz41503-boster.html2026-03-17T05:16:00+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-l2efl-cryab-dz41507-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-wolbachia-wtpre-pifa-dz41517-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-spc25-dz41521-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-african-malaria-mosquito-spz1-dz41524-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-sea-anemone-nv-haaf-dz41528-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-sea-anemone-nve7852-fbcd1-like10-dz41530-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-chlamydomonas-smithii-sag1-ha-plus-agglutinin-dz41531-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-nuf2-dz41533-boster.html2026-03-10T04:37:19+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-hiv-1-vif-dz41534-boster.html2026-03-10T04:37:20+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-herpesvirus-4-bdlf1-dz41535-boster.html2026-03-10T04:37:20+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-polychaete-worm-tdp-43-dz41541-boster.html2026-03-10T04:37:20+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1259582026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00122-2-prap1-primary-antibodies-wb-testing-1.jpgAnti-PARP1 Antibody Picoband® Western blot analysis of PARP1 using anti-PARP1 antibody (A00122-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PARP1 antigen affinity purified polyclonal antibody (Catalog # A00122-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PARP1 at approximately 113 kDa. The expected band size for PARP1 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00122-2-parp1-primary-antibodies-wb-testing-2.jpgAnti-PARP1 Antibody Picoband® Western blot analysis of PARP1 using anti-PARP1 antibody (A00122-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela- WT whole cell lysates, Lane 2: human Hela-GPX4 KO whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. Then the membrane was incubated with rabbit anti-PARP1 antigen affinity purified polyclonal antibody (A00122-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PARP1 at approximately 118 kDa. The expected band size for PARP1 is at 118 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00122-2-prap1-primary-antibodies-if-testing-3.jpgAnti-PARP1 Antibody Picoband® IF analysis of PARP1 using anti-PARP1 antibody (A00122-2) and anti-Beta Tubulin antibody (M01857-3). PARP1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PARP1 Antibody (A00122-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00122-2-prap1-primary-antibodies-fcm-testing-4.pngAnti-PARP1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PARP1 antibody (A00122-2). Overlay histogram showing JK cells stained with A00122-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PARP1 Antibody (A00122-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259592026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09882-1-psmd13-primary-antibodies-wb-testing-1.jpgAnti-PSMD13 Antibody Picoband® Western blot analysis of PSMD13 using anti-PSMD13 antibody (A09882-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse lung tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSMD13 antigen affinity purified polyclonal antibody (Catalog # A09882-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSMD13 at approximately 43 kDa. The expected band size for PSMD13 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09882-1-psmd13-primary-antibodies-fcm-testing-2.pngAnti-PSMD13 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PSMD13 antibody (A09882-1). Overlay histogram showing Hela cells stained with A09882-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSMD13 Antibody (A09882-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09882-1-psmd13-primary-antibodies-ip-testing-1.jpgAnti-PSMD13 Antibody Picoband®Immunoprecipitating (IP) PSMD13 in HepG2 whole cell lysate. Western blot analysis of PSMD13 using anti-PSMD13 antibody (A09882-1); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-PSMD13 antibody in HepG2 whole cell lysate; Lane 3: anti-PSMD13 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PSMD13 antigen affinity purified polyclonal antibody (A09882-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PSMD13 at approximately 43 kDa. The expected band size for PSMD13 is at 43 kDa. https://www.bosterbio.com/catalog/product/view/id/1259602026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04844-1-pstpip1-primary-antibodies-wb-testing-1.jpgAnti-PSTPIP1 Antibody Picoband® Western blot analysis of PSTPIP1 using anti-PSTPIP1 antibody (A04844-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSTPIP1 antigen affinity purified polyclonal antibody (Catalog # A04844-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSTPIP1 at approximately 45 kDa. The expected band size for PSTPIP1 is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04844-1-pstpip1-primary-antibodies-fcm-testing-2.pngAnti-PSTPIP1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PSTPIP1 antibody (A04844-1). Overlay histogram showing JK cells stained with A04844-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSTPIP1 Antibody (A04844-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259612026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-wb-testing-1.jpgAnti-PTCD1 Antibody Picoband® Western blot analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTCD1 antigen affinity purified polyclonal antibody (Catalog # A13208-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTCD1 at approximately 79 kDa. The expected band size for PTCD1 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-2.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-3.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-4.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-5.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-6.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-7.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-8.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-ihc-testing-9.jpgAnti-PTCD1 Antibody Picoband® IHC analysis of PTCD1 using anti-PTCD1 antibody (A13208-1). PTCD1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTCD1 Antibody (A13208-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13208-1-ptcd1-primary-antibodies-fcm-testing-10.pngAnti-PTCD1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-PTCD1 antibody (A13208-1). Overlay histogram showing 293T cells stained with A13208-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PTCD1 Antibody (A13208-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259622026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02548-1-ptger3-primary-antibodies-wb-testing-1.jpgAnti-PTGER3 Antibody Picoband® Western blot analysis of PTGER3 using anti-PTGER3 antibody (A02548-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTGER3 antigen affinity purified polyclonal antibody (Catalog # A02548-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTGER3 at approximately 48 kDa. The expected band size for PTGER3 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02548-1-ptger3-primary-antibodies-fcm-testing-2.pngAnti-PTGER3 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-PTGER3 antibody (A02548-1). Overlay histogram showing THP-1 cells stained with A02548-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PTGER3 Antibody (A02548-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259632026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08739-1-nap1l4-primary-antibodies-wb-testing-1.jpgAnti-NAP1L4 Antibody Picoband® Western blot analysis of NAP1L4 using anti-NAP1L4 antibody (A08739-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAP1L4 antigen affinity purified polyclonal antibody (Catalog # A08739-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAP1L4 at approximately 65 kDa. The expected band size for NAP1L4 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08739-1-nap1l4-primary-antibodies-fcm-testing-2.pngAnti-NAP1L4 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NAP1L4 antibody (A08739-1). Overlay histogram showing 293T cells stained with A08739-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAP1L4 Antibody (A08739-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259642026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07040-1-nelfa-primary-antibodies-wb-testing-1.jpgAnti-NELFA Antibody Picoband® Western blot analysis of NELFA using anti-NELFA antibody (A07040-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NELFA antigen affinity purified polyclonal antibody (Catalog # A07040-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NELFA at approximately 57 kDa. The expected band size for NELFA is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07040-1-nelfa-primary-antibodies-fcm-testing-2.pngAnti-NELFA Antibody Picoband® Flow Cytometry analysis of JK cells using anti-NELFA antibody (A07040-1). Overlay histogram showing JK cells stained with A07040-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NELFA Antibody (A07040-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259652026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08303-1-neto1-primary-antibodies-wb-testing-1.jpgAnti-NETO1 Antibody Picoband® Western blot analysis of NETO1 using anti-NETO1 antibody (A08303-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse RM-1 whole cell lysates, Lane 8: mouse SP2/0 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NETO1 antigen affinity purified polyclonal antibody (Catalog # A08303-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NETO1 at approximately 70 kDa. The expected band size for NETO1 is at 60 kDa. https://www.bosterbio.com/catalog/product/view/id/1259662026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09555-1-neto2-primary-antibodies-wb-testing-1.jpgAnti-NETO2 Antibody Picoband® Western blot analysis of NETO2 using anti-NETO2 antibody (A09555-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SIHA whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NETO2 antigen affinity purified polyclonal antibody (Catalog # A09555-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NETO2 at approximately 65 kDa. The expected band size for NETO2 is at 59 kDa. https://www.bosterbio.com/catalog/product/view/id/1259672026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05061-1-nfs1-primary-antibodies-wb-testing-1.jpgAnti-NFS1 Antibody Picoband® Western blot analysis of NFS1 using anti-NFS1 antibody (A05061-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse HEPA1-6 whole cell lysates, Lane 8: mouse B16-F10 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFS1 antigen affinity purified polyclonal antibody (Catalog # A05061-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NFS1 at approximately 45 kDa. The expected band size for NFS1 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05061-1-nfs1-primary-antibodies-fcm-testing-2.pngAnti-NFS1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NFS1 antibody (A05061-1). Overlay histogram showing HEL cells stained with A05061-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFS1 Antibody (A05061-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05061-1-nfs1-primary-antibodies-ip-testing-3.jpgAnti-NFS1 Antibody Picoband® Immunoprecipitating NFS1 in HepG2 whole cell lysate. Western blot analysis of NFS1 using anti-NFS1 antibody (A05061-1); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-NFS1 antibody in HepG2 whole cell lysate; Lane 3: anti-NFS1 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NFS1 antigen affinity purified polyclonal antibody (A05061-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NFS1 at approximately 45 kDa. The expected band size for NFS1 is at 50 kDa. https://www.bosterbio.com/catalog/product/view/id/1259682026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02676-2-nnmt-primary-antibodies-wb-testing-1_1.jpgAnti-NNMT Antibody Picoband®Western blot analysis of NNMT using anti-NNMT antibody (A02676-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NNMT antigen affinity purified polyclonal antibody (Catalog # A02676-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NNMT at approximately 30 kDa. The expected band size for NNMT is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02676-2-nnmt-primary-antibodies-if-testing-1.jpgAnti-NNMT Antibody Picoband®IF analysis of NNMT using anti-NNMT antibody (A02676-2). NNMT was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NNMT Antibody (A02676-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02676-2-nnmt-primary-antibodies-ip-testing-1.jpgAnti-NNMT Antibody Picoband®Immunoprecipitating (IP) NNMT in Hela whole cell lysate. Western blot analysis of NNMT using anti-NNMT antibody (A02676-2); Lane 1: Hela whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-NNMT antibody in Hela whole cell lysate; Lane 3: anti-NNMT antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NNMT antigen affinity purified polyclonal antibody (A02676-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NNMT at approximately 30 kDa. The expected band size for NNMT is at 30 kDa. https://www.bosterbio.com/catalog/product/view/id/1259692026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02817-1-plcb1-primary-antibodies-wb-testing-1.jpgAnti-PLCB1 Antibody Picoband® Western blot analysis of PLCB1 using anti-PLCB1 antibody (A02817-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLCB1 antigen affinity purified polyclonal antibody (Catalog # A02817-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLCB1 at approximately 150 kDa. The expected band size for PLCB1 is at 138 kDa. https://www.bosterbio.com/catalog/product/view/id/1259702026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-wb-testing-1.jpgAnti-PTRHD1 Antibody Picoband® Western blot analysis of PTRHD1 using anti-PTRHD1 antibody (A17455). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293Tt whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTRHD1 antigen affinity purified polyclonal antibody (Catalog # A17455) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTRHD1 at approximately 16 kDa. The expected band size for PTRHD1 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-ihc-testing-6.jpgAnti-PTRHD1 Antibody Picoband®IHC analysis of C2orf79/PTRHD1 using anti-C2orf79/PTRHD1 antibody (A17455). C2orf79/PTRHD1 was detected in a paraffin-embedded section of human cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C2orf79/PTRHD1 Antibody (A17455) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-ihc-testing-2.jpgAnti-PTRHD1 Antibody Picoband® IHC analysis of PTRHD1 using anti-PTRHD1 antibody (A17455). PTRHD1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTRHD1 Antibody (A17455) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-ihc-testing-3.jpgAnti-PTRHD1 Antibody Picoband® IHC analysis of PTRHD1 using anti-PTRHD1 antibody (A17455). PTRHD1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTRHD1 Antibody (A17455) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-ihc-testing-4.jpgAnti-PTRHD1 Antibody Picoband® IHC analysis of PTRHD1 using anti-PTRHD1 antibody (A17455). PTRHD1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTRHD1 Antibody (A17455) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-ihc-testing-5.jpgAnti-PTRHD1 Antibody Picoband® IHC analysis of PTRHD1 using anti-PTRHD1 antibody (A17455). PTRHD1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PTRHD1 Antibody (A17455) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-if-testing-6.jpgAnti-PTRHD1 Antibody Picoband® IF analysis of PTRHD1 using anti-PTRHD1 antibody (A17455) and anti-Beta Tubulin antibody (M01857-3). PTRHD1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PTRHD1 Antibody (A17455) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17455-ptrhd1-primary-antibodies-fcm-testing-7.pngAnti-PTRHD1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PTRHD1 antibody (A17455). Overlay histogram showing RT4 cells stained with A17455 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PTRHD1 Antibody (A17455, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259712026-03-17T05:16:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03331-3-nrih3-primary-antibodies-wb-testing-1.jpgAnti-NR1H3 Antibody Picoband® Western blot analysis of NR1H3 using anti-NR1H3 antibody (A03331-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NR1H3 antigen affinity purified polyclonal antibody (Catalog # A03331-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NR1H3 at approximately 50 kDa. The expected band size for NR1H3 is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03331-3-nrih3-primary-antibodies-fcm-testing-2.pngAnti-NR1H3 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-NR1H3 antibody (A03331-3). Overlay histogram showing RT4 cells stained with A03331-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NR1H3 Antibody (A03331-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259722026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-wb-testing-1.jpgAnti-MED4 Antibody Picoband® Western blot analysis of MED4 using anti-MED4 antibody (A06467-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MOLT-4 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: rat NRK whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates, Lane 7: mouse ANA-1 whole cell lysates, Lane 8: mouse EL-4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED4 antigen affinity purified polyclonal antibody (Catalog # A06467-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED4 at approximately 37 kDa. The expected band size for MED4 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-ihc-testing-2.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-3). MED4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED4 Antibody (A06467-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-ihc-testing-3.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-3). MED4 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED4 Antibody (A06467-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-ihc-testing-4.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-3). MED4 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED4 Antibody (A06467-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-ihc-testing-5.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-3). MED4 was detected in a paraffin-embedded section of human rectum adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED4 Antibody (A06467-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-ihc-testing-6.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-3). MED4 was detected in a paraffin-embedded section of human spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED4 Antibody (A06467-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-ihc-testing-7.jpgAnti-MED4 Antibody Picoband® IHC analysis of MED4 using anti-MED4 antibody (A06467-3). MED4 was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MED4 Antibody (A06467-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-if-testing-8.jpgAnti-MED4 Antibody Picoband® IF analysis of MED4 using anti-MED4 antibody (A06467-3) and anti-Beta Tubulin antibody (M01857-3). MED4 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MED4 Antibody (A06467-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06467-3-med4-primary-antibodies-fcm-testing-9.pngAnti-MED4 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MED4 antibody (A06467-3). Overlay histogram showing JK cells stained with A06467-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED4 Antibody (A06467-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259732026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-wb-testing-1.jpgAnti-MELTF Antibody Picoband® Western blot analysis of MELTF using anti-MELTF antibody (A12988-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MELTF antigen affinity purified polyclonal antibody (Catalog # A12988-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MELTF at approximately 90 kDa. The expected band size for MELTF is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-wb-testing-2.jpgAnti-MELTF Antibody Picoband® Western blot analysis of MELTF using anti-MELTF antibody (A12988-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skin tissue lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse skin tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MELTF antigen affinity purified polyclonal antibody (Catalog # A12988-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MELTF at approximately 90 kDa. The expected band size for MELTF is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-ihc-testing-3.jpgAnti-MELTF Antibody Picoband® IHC analysis of MELTF using anti-MELTF antibody (A12988-1). MELTF was detected in a paraffin-embedded section of human melanoma cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELTF Antibody (A12988-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-ihc-testing-4.jpgAnti-MELTF Antibody Picoband® IHC analysis of MELTF using anti-MELTF antibody (A12988-1). MELTF was detected in a paraffin-embedded section of human melanoma cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELTF Antibody (A12988-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-ihc-testing-5.jpgAnti-MELTF Antibody Picoband® IHC analysis of MELTF using anti-MELTF antibody (A12988-1). MELTF was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELTF Antibody (A12988-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-ihc-testing-6.jpgAnti-MELTF Antibody Picoband® IHC analysis of MELTF using anti-MELTF antibody (A12988-1). MELTF was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELTF Antibody (A12988-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-ihc-testing-7.jpgAnti-MELTF Antibody Picoband® IHC analysis of MELTF using anti-MELTF antibody (A12988-1). MELTF was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELTF Antibody (A12988-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12988-1-meltf-primary-antibodies-ihc-testing-8.jpgAnti-MELTF Antibody Picoband® IHC analysis of MELTF using anti-MELTF antibody (A12988-1). MELTF was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MELTF Antibody (A12988-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1259742026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06392-1-mep1b-primary-antibodies-wb-testing-1_1.jpgAnti-MEP1B Antibody Picoband® Western blot analysis of MEP1B using anti-MEP1B antibody (A06392-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat small intestine tissue lysates, Lane 2: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEP1B antigen affinity purified polyclonal antibody (Catalog # A06392-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MEP1B at approximately 97 kDa. The expected band size for MEP1B is at 80 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06392-1-mep1b-primary-antibodies-ihc-testing-2_1.jpgAnti-MEP1B Antibody Picoband® IHC analysis of MEP1B using anti-MEP1B antibody (A06392-1). MEP1B was detected in a paraffin-embedded section of mouse intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MEP1B Antibody (A06392-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06392-1-mep1b-primary-antibodies-ihc-testing-3_1.jpgAnti-MEP1B Antibody Picoband® IHC analysis of MEP1B using anti-MEP1B antibody (A06392-1). MEP1B was detected in a paraffin-embedded section of rat intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MEP1B Antibody (A06392-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06392-1-mep1b-primary-antibodies-if-testing-4.jpgAnti-MEP1B Antibody Picoband® IF analysis of MEP1B using anti-MEP1B antibody (A06392-1). MEP1B was detected in paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MEP1B Antibody (A06392-1) overnight at 4°C. Dylight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06392-1-mep1b-primary-antibodies-if-testing-5.jpgAnti-MEP1B Antibody Picoband® IF analysis of MEP1B using anti-MEP1B antibody (A06392-1). MEP1B was detected in paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5μg/mL rabbit anti-MEP1B Antibody (A06392-1) overnight at 4°C. Dylight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1259752026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07241-1-mest-primary-antibodies-wb-testing-1.jpgAnti-MEST Antibody Picoband® Western blot analysis of MEST using anti-MEST antibody (A07241-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEST antigen affinity purified polyclonal antibody (Catalog # A07241-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MEST at approximately 43 kDa. The expected band size for MEST is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07241-1-mest-primary-antibodies-ihc-testing-2.jpgAnti-MEST Antibody Picoband® IHC analysis of MEST using anti-MEST antibody (A07241-1). MEST was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MEST Antibody (A07241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07241-1-mest-primary-antibodies-ihc-testing-3.jpgAnti-MEST Antibody Picoband® IHC analysis of MEST using anti-MEST antibody (A07241-1). MEST was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MEST Antibody (A07241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07241-1-mest-primary-antibodies-ihc-testing-4.jpgAnti-MEST Antibody Picoband® IHC analysis of MEST using anti-MEST antibody (A07241-1). MEST was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MEST Antibody (A07241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1259762026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11383-1-metrnl-primary-antibodies-wb-testing-1.jpgAnti-METRNL Antibody Picoband® Western blot analysis of Meteorin-like/METRNL using anti-Meteorin-like/METRNL antibody (A11383-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Meteorin-like/METRNL antigen affinity purified polyclonal antibody (Catalog # A11383-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Meteorin-like/METRNL at approximately 34 kDa. The expected band size for Meteorin-like/METRNL is at 34 kDa. https://www.bosterbio.com/catalog/product/view/id/1259772026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08611-2-med28-primary-antibodies-wb-testing-1.jpgAnti-MED28 Antibody Picoband® Western blot analysis of MED28 using anti-MED28 antibody (A08611-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MED28 antigen affinity purified polyclonal antibody (Catalog # A08611-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MED28 at approximately 24 kDa. The expected band size for MED28 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08611-2-med28-primary-antibodies-fcm-testing-2.pngAnti-MED28 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-MED28 antibody (A08611-2). Overlay histogram showing THP-1 cells stained with A08611-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MED28 Antibody (A08611-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08611-2-med28-primary-antibodies-ip-testing-3..jpgAnti-MED28 Antibody Picoband® Immunoprecipitating MED28 in HepG2 whole cell lysate. Western blot analysis of MED28 using anti-MED28 antibody (A08611-2); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-MED28 antibody in HepG2 whole cell lysate; Lane 3: anti-MED28 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MED28 antigen affinity purified polyclonal antibody (A08611-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for MED28 at approximately 24 kDa. The expected band size for MED28 is at 20 kDa. https://www.bosterbio.com/catalog/product/view/id/1259782026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12581-mfap3l-primary-antibodies-wb-testing-1.jpgAnti-MFAP3L Antibody Picoband® Western blot analysis of MFAP3L using anti-MFAP3L antibody (A12581). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MFAP3L antigen affinity purified polyclonal antibody (Catalog # A12581) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MFAP3L at approximately 45 kDa. The expected band size for MFAP3L is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12581-mfap3l-primary-antibodies-if-testing-2.jpgAnti-MFAP3L Antibody Picoband® IF analysis of MFAP3L using anti-MFAP3L antibody (A12581). MFAP3L was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MFAP3L Antibody (A12581) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1259792026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16307-1-lmntd1-primary-antibodies-wb-testing-1.jpgAnti-LMNTD1 Antibody Picoband® Western blot analysis of IFTLD1/LMNTD1 using anti-IFTLD1/LMNTD1 antibody (A16307-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFTLD1/LMNTD1 antigen affinity purified polyclonal antibody (Catalog # A16307-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFTLD1/LMNTD1 at approximately 43 kDa. The expected band size for IFTLD1/LMNTD1 is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16307-1-lmntd1-primary-antibodies-fcm-testing-2.pngAnti-LMNTD1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-IFTLD1/LMNTD1 antibody (A16307-1). Overlay histogram showing RT4 cells stained with A16307-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFTLD1/LMNTD1 Antibody (A16307-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16307-1-lmntd1-primary-antibodies-fcm-testing-3.pngAnti-LMNTD1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-IFTLD1/LMNTD1 antibody (A16307-1). Overlay histogram showing SH-SY5Y cells stained with A16307-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFTLD1/LMNTD1 Antibody (A16307-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259802026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32469-1-mettl26-primary-antibodies-wb-testing-1.jpgAnti-METTL26 Antibody Picoband® Western blot analysis of METTL26 using anti-METTL26 antibody (A32469-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METTL26 antigen affinity purified polyclonal antibody (Catalog # A32469-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METTL26 at approximately 23 kDa. The expected band size for METTL26 is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32469-1-mettl26-primary-antibodies-fcm-testing-2.pngAnti-METTL26 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-METTL26 antibody (A32469-1). Overlay histogram showing THP-1 cells stained with A32469-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-METTL26 Antibody (A32469-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259812026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16078-1-mfsd4a-primary-antibodies-wb-testing-1.jpgAnti-MFSD4A Antibody Picoband® Western blot analysis of MFSD4A using anti-MFSD4A antibody (A16078-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human HepG2 whole cell lysates After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MFSD4A antigen affinity purified polyclonal antibody (Catalog # A16078-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MFSD4A at approximately 68 kDa. The expected band size for MFSD4A is at 56 kDa. https://www.bosterbio.com/catalog/product/view/id/1259822026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08089-mical3-primary-antibodies-wb-testing-1.jpgAnti-MICAL3 Antibody Picoband® Western blot analysis of MICAL3 using anti-MICAL3 antibody (A08089). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MICAL3 antigen affinity purified polyclonal antibody (Catalog # A08089) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MICAL3 at approximately 224-280 kDa. The expected band size for MICAL3 is at 224 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08089-mical3-primary-antibodies-fcm-testing-2.pngAnti-MICAL3 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-MICAL3 antibody (A08089). Overlay histogram showing U251 cells stained with A08089 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MICAL3 Antibody (A08089, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259832026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-wb-testing-1.jpgAnti-MICALL1 Antibody Picoband® Western blot analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MICALL1 antigen affinity purified polyclonal antibody (Catalog # A09767-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MICALL1 at approximately 145 kDa. The expected band size for MICALL1 is at 93 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-2.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-3.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-4_1.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-5_1.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-6.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-7.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-8.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-9.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-10.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-11.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-12.jpgAnti-MICALL1 Antibody Picoband® IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-ihc-testing-13_1.jpgAnti-MICALL1 Antibody Picoband®IHC analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-if-testing-1.jpgAnti-MICALL1 Antibody Picoband®IF analysis of MICALL1 using anti-MICALL1 antibody (A09767-1). MICALL1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MICALL1 Antibody (A09767-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09767-1-micall1-primary-antibodies-fcm-testing-14.pngAnti-MICALL1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MICALL1 antibody (A09767-1). Overlay histogram showing MCF-7 cells stained with A09767-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MICALL1 Antibody (A09767-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259842026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06957-miox-primary-antibodies-wb-testing-1.jpgAnti-MIOX Antibody Picoband® Western blot analysis of MIOX using anti-MIOX antibody (A06957). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIOX antigen affinity purified polyclonal antibody (Catalog # A06957) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIOX at approximately 36 kDa. The expected band size for MIOX is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06957-miox-primary-antibodies-ihc-testing-5.jpgAnti-MIOX Antibody Picoband®IHC analysis of MIOX using anti-MIOX antibody (A06957). MIOX was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIOX Antibody (A06957) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06957-miox-primary-antibodies-wb-testing-2.jpgAnti-MIOX Antibody Picoband® Western blot analysis of MIOX using anti-MIOX antibody (A06957). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MIOX antigen affinity purified polyclonal antibody (Catalog # A06957) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MIOX at approximately 36 kDa. The expected band size for MIOX is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06957-miox-primary-antibodies-ihc-testing-3.jpgAnti-MIOX Antibody Picoband® IHC analysis of MIOX using anti-MIOX antibody (A06957). MIOX was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIOX Antibody (A06957) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06957-miox-primary-antibodies-ihc-testing-4.jpgAnti-MIOX Antibody Picoband® IHC analysis of MIOX using anti-MIOX antibody (A06957). MIOX was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MIOX Antibody (A06957) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06957-miox-primary-antibodies-fcm-testing-5.pngAnti-MIOX Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MIOX antibody (A06957). Overlay histogram showing JK cells stained with A06957 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MIOX Antibody (A06957, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259852026-03-17T05:16:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06081-3-mlph-primary-antibodies-wb-testing-1.jpgAnti-MLPH Antibody Picoband® Western blot analysis of Melanophilin/MLPH using anti-Melanophilin/MLPH antibody (A06081-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Melanophilin/MLPH antigen affinity purified polyclonal antibody (Catalog # A06081-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Melanophilin/MLPH at approximately 85 kDa. The expected band size for Melanophilin/MLPH is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06081-3-mlph-primary-antibodies-if-testing-2.jpgAnti-MLPH Antibody Picoband® IF analysis of Melanophilin/MLPH using anti-Melanophilin/MLPH antibody (A06081-3). Melanophilin/MLPH was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Melanophilin/MLPH Antibody (A06081-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1259862026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00659-3-foxm1-primary-antibodies-wb-testing-1.jpgAnti-FOXM1 Antibody Picoband® Western blot analysis of FOXM1 using anti-FOXM1 antibody (A00659-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human DLD-1 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human U2OS whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOXM1 antigen affinity purified polyclonal antibody (Catalog # A00659-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FOXM1 at approximately 110 kDa. The expected band size for FOXM1 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00659-3-foxm1-primary-antibodies-if-testing-2.jpgAnti-FOXM1 Antibody Picoband® IF analysis of FOXM1 using anti-FOXM1 antibody (A00659-3) and anti-Beta Tubulin antibody (M01857-3). FOXM1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-FOXM1 Antibody (A00659-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00659-3-foxm1-primary-antibodies-fcm-testing-3.pngAnti-FOXM1 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-FOXM1 antibody (A00659-3). Overlay histogram showing Hela cells stained with A00659-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FOXM1 Antibody (A00659-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259872026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09180-1-mylk3-primary-antibodies-wb-testing-1.jpgAnti-MYLK3 Antibody Picoband® Western blot analysis of MYLK3 using anti-MYLK3 antibody (A09180-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYLK3 antigen affinity purified polyclonal antibody (Catalog # A09180-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYLK3 at approximately 100 kDa. The expected band size for MYLK3 is at 88 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09180-1-mylk3-primary-antibodies-fcm-testing-2.pngAnti-MYLK3 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-MYLK3 antibody (A09180-1). Overlay histogram showing HEL cells stained with A09180-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYLK3 Antibody (A09180-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259882026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04663-2-myot-primary-antibodies-wb-testing-1.jpgAnti-MYOT Antibody Picoband® Western blot analysis of MYOT using anti-MYOT antibody (A04663-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat skeletal muscle tissue lysates, Lane 6: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYOT antigen affinity purified polyclonal antibody (Catalog # A04663-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYOT at approximately 55 kDa. The expected band size for MYOT is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04663-2-myot-primary-antibodies-ihc-testing-2.jpgAnti-MYOT Antibody Picoband® IHC analysis of MYOT using anti-MYOT antibody (A04663-2). MYOT was detected in a paraffin-embedded section of human skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYOT Antibody (A04663-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04663-2-myot-primary-antibodies-if-testing-3.jpgAnti-MYOT Antibody Picoband® IF analysis of MYOT using anti-MYOT antibody (A04663-2). MYOT was detected in an immunocytochemical section of GES-1 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MYOT Antibody (A04663-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04663-2-myot-primary-antibodies-fcm-testing-4.jpgAnti-MYOT Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MYOT antibody (A04663-2). Overlay histogram showing JK cells stained with A04663-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYOT Antibody (A04663-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1259892026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00621-1-lgals3-primary-antibodies-wb-testing-1.jpgAnti-LGALS3 Antibody Picoband® Western blot analysis of Galectin-3/LGALS3 using anti-Galectin-3/LGALS3 antibody (A00621-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat stomach tissue lysates, Lane 6: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Galectin-3/LGALS3 antigen affinity purified polyclonal antibody (Catalog # A00621-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Galectin-3/LGALS3 at approximately 29 kDa. The expected band size for Galectin-3/LGALS3 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00621-1-lgals3-primary-antibodies-if-testing-2.jpgAnti-LGALS3 Antibody Picoband® IF analysis of Galectin-3/LGALS3 using anti-Galectin-3/LGALS3 antibody (A00621-1). Galectin-3/LGALS3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Galectin-3/LGALS3 Antibody (A00621-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1259902026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02938-2-lgals3bp-primary-antibodies-wb-testing-1.jpgAnti-LGALS3BP Antibody Picoband® Western blot analysis of LGALS3BP using anti-LGALS3BP antibody (A02938-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human COLO 320 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LGALS3BP antigen affinity purified polyclonal antibody (Catalog # A02938-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LGALS3BP at approximately 70-90 kDa. The expected band size for LGALS3BP is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02938-2-lgals3bp-primary-antibodies-if-testing-2.jpgAnti-LGALS3BP Antibody Picoband® IF analysis of LGALS3BP using anti-LGALS3BP antibody (A02938-2). LGALS3BP was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LGALS3BP Antibody (A02938-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02938-2-lgals3bp-primary-antibodies-fcm-testing-3.pngAnti-LGALS3BP Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-LGALS3BP antibody (A02938-2). Overlay histogram showing HepG2 cells stained with A02938-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LGALS3BP Antibody (A02938-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259912026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12658-1-lingo2-primary-antibodies-wb-testing-1.jpgAnti-LINGO2 Antibody Picoband® Western blot analysis of LINGO2 using anti-LINGO2 antibody (A12658-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LINGO2 antigen affinity purified polyclonal antibody (Catalog # A12658-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LINGO2 at approximately 68 kDa. The expected band size for LINGO2 is at 68 kDa. https://www.bosterbio.com/catalog/product/view/id/1259922026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08503-1-llgl2-primary-antibodies-wb-testing-1.jpgAnti-LLGL2 Antibody Picoband® Western blot analysis of LLGL2 using anti-LLGL2 antibody (A08503-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LLGL2 antigen affinity purified polyclonal antibody (Catalog # A08503-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LLGL2 at approximately 120 kDa. The expected band size for LLGL2 is at 113 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08503-1-llgl2-primary-antibodies-fcm-testing-2.pngAnti-LLGL2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-LLGL2 antibody (A08503-1). Overlay histogram showing HepG2 cells stained with A08503-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LLGL2 Antibody (A08503-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259932026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06721-1-lpar5-primary-antibodies-wb-testing-1.jpgAnti-LPAR5 Antibody Picoband® Western blot analysis of GPR92/LPAR5 using anti-GPR92/LPAR5 antibody (A06721-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GPR92/LPAR5 antigen affinity purified polyclonal antibody (Catalog # A06721-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GPR92/LPAR5 at approximately 41 kDa. The expected band size for GPR92/LPAR5 is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06721-1-lpar5-primary-antibodies-fcm-testing-2.pngAnti-LPAR5 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-GPR92/LPAR5 antibody (A06721-1). Overlay histogram showing K562 cells stained with A06721-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GPR92/LPAR5 Antibody (A06721-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259942026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17988-1-lrrc71-primary-antibodies-wb-testing-1.jpgAnti-LRRC71 Antibody Picoband® Western blot analysis of C1orf92/LRRC71 using anti-C1orf92/LRRC71 antibody (A17988-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human U2OS whole cell lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C1orf92/LRRC71 antigen affinity purified polyclonal antibody (Catalog # A17988-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C1orf92/LRRC71 at approximately 62 kDa. The expected band size for C1orf92/LRRC71 is at 62 kDa. https://www.bosterbio.com/catalog/product/view/id/1259952026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02992-2-lsp1-primary-antibodies-wb-testing-1.jpgAnti-LSP1 Antibody Picoband® Western blot analysis of LSP1 using anti-LSP1 antibody (A02992-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HL-60 whole cell lysates, Lane 2: human U-937 whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human Daudi whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: rat thymus tissue lysates, Lane 7: mouse spleen tissue lysates, Lane 8: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LSP1 antigen affinity purified polyclonal antibody (Catalog # A02992-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LSP1 at approximately 52 kDa. The expected band size for LSP1 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02992-2-lsp1-primary-antibodies-fcm-testing-2.pngAnti-LSP1 Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-LSP1 antibody (A02992-2). Overlay histogram showing U937 cells stained with A02992-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LSP1 Antibody (A02992-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259962026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00942-2-ltbr-primary-antibodies-wb-testing-1.jpgAnti-LTBR Antibody Picoband® Western blot analysis of LTBR using anti-LTBR antibody (A00942-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Hut-78 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LTBR antigen affinity purified polyclonal antibody (Catalog # A00942-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LTBR at approximately 55-60 kDa. The expected band size for LTBR is at 47 kDa. https://www.bosterbio.com/catalog/product/view/id/1259972026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12616-1-luzp1-primary-antibodies-wb-testing-1.jpgAnti-LUZP1 Antibody Picoband® Western blot analysis of LUZP1 using anti-LUZP1 antibody (A12616-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LUZP1 antigen affinity purified polyclonal antibody (Catalog # A12616-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LUZP1 at approximately 120 kDa. The expected band size for LUZP1 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12616-1-luzp1-primary-antibodies-ihc-testing-1.jpgAnti-LUZP1 Antibody Picoband®IHC analysis of LUZP1 using anti-LUZP1 antibody (A12616-1). LUZP1 was detected in a paraffin-embedded section of human cerebral cortex tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LUZP1 Antibody (A12616-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12616-1-luzp1-primary-antibodies-if-testing-2.jpgAnti-LUZP1 Antibody Picoband® IF analysis of LUZP1 using anti-LUZP1 antibody (A12616-1) and anti-Beta Tubulin antibody (M01857-3). LUZP1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LUZP1 Antibody (A12616-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12616-1-luzp1-primary-antibodies-fcm-testing-3.pngAnti-LUZP1 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-LUZP1 antibody (A12616-1). Overlay histogram showing A431 cells stained with A12616-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LUZP1 Antibody (A12616-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1259982026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09680-ly6d-primary-antibodies-wb-testing-1.jpgAnti-LY6D Antibody Picoband® Western blot analysis of LY6D using anti-LY6D antibody (A09680). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LY6D antigen affinity purified polyclonal antibody (Catalog # A09680) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LY6D at approximately 16 kDa. The expected band size for LY6D is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09680-ly6d-primary-antibodies-ihc-testing-2.jpgAnti-LY6D Antibody Picoband® IHC analysis of LY6D using anti-LY6D antibody (A09680). LY6D was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LY6D Antibody (A09680) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1259992026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09986-2-lyar-primary-antibodies-wb-testing-1.jpgAnti-LYAR Antibody Picoband® Western blot analysis of LYAR using anti-LYAR antibody (A09986-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat RH-35 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LYAR antigen affinity purified polyclonal antibody (Catalog # A09986-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LYAR at approximately 44 kDa. The expected band size for LYAR is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09986-2-lyar-primary-antibodies-if-testing-2.jpgAnti-LYAR Antibody Picoband® IF analysis of LYAR using anti-LYAR antibody (A09986-2) and anti-Beta Tubulin antibody (M01857-3). LYAR was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LYAR Antibody (A09986-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09986-2-lyar-primary-antibodies-ip-testing-1.jpgAnti-LYAR Antibody Picoband®Immunoprecipitating (IP) LYAR in K562 whole cell lysate. Western blot analysis of LYAR using anti-LYAR antibody (A09986-2); Lane 1: K562 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-LYAR antibody in K562 whole cell lysate; Lane 3: anti-LYAR antibody (2μg) + K562 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-LYAR antigen affinity purified polyclonal antibody (A09986-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for LYAR at approximately 44 kDa. The expected band size for LYAR is at 44 kDa. https://www.bosterbio.com/catalog/product/view/id/1260002026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07611-1-jade1-primary-antibodies-wb-testing-1.jpgAnti-JADE1 Antibody Picoband® Western blot analysis of PHF17/JADE1 using anti-PHF17/JADE1 antibody (A07611-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHF17/JADE1 antigen affinity purified polyclonal antibody (Catalog # A07611-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHF17/JADE1 at approximately 96 kDa. The expected band size for PHF17/JADE1 is at 96 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07611-1-jade1-primary-antibodies-if-testing-2.jpgAnti-JADE1 Antibody Picoband® IF analysis of PHF17/JADE1 using anti-PHF17/JADE1 antibody (A07611-1) and anti-Beta Tubulin antibody (M01857-3). PHF17/JADE1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PHF17/JADE1 Antibody (A07611-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07611-1-jade1-primary-antibodies-fcm-testing-3.pngAnti-JADE1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-PHF17/JADE1 antibody (A07611-1). Overlay histogram showing K562 cells stained with A07611-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHF17/JADE1 Antibody (A07611-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260012026-03-17T05:16:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05754-4-ifi30-primary-antibodies-wb-testing-1.jpgAnti-IFI30 Antibody Picoband® Western blot analysis of IFI30 using anti-IFI30 antibody (A05754-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat spleen tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFI30 antigen affinity purified polyclonal antibody (Catalog # A05754-4) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFI30 at approximately 23 kDa. The expected band size for IFI30 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05754-4-ifi30-primary-antibodies-fcm-testing-2.pngAnti-IFI30 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-IFI30 antibody (A05754-4). Overlay histogram showing HepG2 cells stained with A05754-4 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-IFI30 Antibody (A05754-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260022026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04613-2-lrig1-primary-antibodies-wb-testing-1.jpgAnti-LRIG1 Antibody Picoband® Western blot analysis of LRIG1 using anti-LRIG1 antibody (A04613-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRIG1 antigen affinity purified polyclonal antibody (Catalog # A04613-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRIG1 at approximately 145 kDa. The expected band size for LRIG1 is at 119 kDa. https://www.bosterbio.com/catalog/product/view/id/1260032026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08957-trim2-primary-antibodies-wb-testing-1.jpgAnti-TRIM2 Antibody Picoband® Western blot analysis of TRIM2 using anti-TRIM2 antibody (A08957). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIM2 antigen affinity purified polyclonal antibody (Catalog # A08957) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRIM2 at approximately 82 kDa. The expected band size for TRIM2 is at 82 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08957-trim2-primary-antibodies-ihc-testing-2.jpgAnti-TRIM2 Antibody Picoband® IHC analysis of TRIM2 using anti-TRIM2 antibody (A08957). TRIM2 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM2 Antibody (A08957) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08957-trim2-primary-antibodies-ihc-testing-3.jpgAnti-TRIM2 Antibody Picoband® IHC analysis of TRIM2 using anti-TRIM2 antibody (A08957). TRIM2 was detected in a paraffin-embedded section of human glioblastoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM2 Antibody (A08957) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08957-trim2-primary-antibodies-ihc-testing-4.jpgAnti-TRIM2 Antibody Picoband® IHC analysis of TRIM2 using anti-TRIM2 antibody (A08957). TRIM2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM2 Antibody (A08957) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08957-trim2-primary-antibodies-ihc-testing-5.jpgAnti-TRIM2 Antibody Picoband® IHC analysis of TRIM2 using anti-TRIM2 antibody (A08957). TRIM2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM2 Antibody (A08957) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1260042026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09301-1-lyrm4-primary-antibodies-wb-testing-1.jpgAnti-LYRM4 Antibody Picoband® Western blot analysis of LYRM4 using anti-LYRM4 antibody (A09301-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LYRM4 antigen affinity purified polyclonal antibody (Catalog # A09301-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LYRM4 at approximately 15 kDa. The expected band size for LYRM4 is at 11 kDa. https://www.bosterbio.com/catalog/product/view/id/1260052026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02886-2-gamt-primary-antibodies-wb-testing-1.jpgAnti-GAMT Antibody Picoband® Western blot analysis of GAMT using anti-GAMT antibody (A02886-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAMT antigen affinity purified polyclonal antibody (Catalog # A02886-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAMT at approximately 26 kDa. The expected band size for GAMT is at 26 kDa. https://www.bosterbio.com/catalog/product/view/id/1260062026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09568-pglyrp2-primary-antibodies-wb-testing-1.jpgAnti-PGLYRP2 Antibody Picoband® Western blot analysis of PGLYRP2 using anti-PGLYRP2 antibody (A09568). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH-35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGLYRP2 antigen affinity purified polyclonal antibody (Catalog # A09568) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGLYRP2 at approximately 74 kDa. The expected band size for PGLYRP2 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09568-pglyrp2-primary-antibodies-fcm-testing-2.pngAnti-PGLYRP2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-PGLYRP2 antibody (A09568). Overlay histogram showing K562 cells stained with A09568 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PGLYRP2 Antibody (A09568, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260072026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06581-lpxn-primary-antibodies-wb-testing-1.jpgAnti-LPXN Antibody Picoband® Western blot analysis of LPXN using anti-LPXN antibody (A06581). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human U-87 MG whole cell lysates, Lane 4: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LPXN antigen affinity purified polyclonal antibody (Catalog # A06581) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LPXN at approximately 43 kDa. The expected band size for LPXN is at 43 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06581-lpxn-primary-antibodies-if-testing-2.jpgAnti-LPXN Antibody Picoband® IF analysis of LPXN using anti-LPXN antibody (A06581). LPXN was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LPXN Antibody (A06581) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06581-lpxn-primary-antibodies-fcm-testing-3.pngAnti-LPXN Antibody Picoband® Flow Cytometry analysis of RAJI cells using anti-LPXN antibody (A06581). Overlay histogram showing RAJI cells stained with A06581 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LPXN Antibody (A06581, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260082026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13956-2-lrrc-primary-antibodies-wb-testing-1.jpgAnti-LRRC1 Antibody Picoband® Western blot analysis of LRRC1 using anti-LRRC1 antibody (A13956-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: mouse testis tissue lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC1 antigen affinity purified polyclonal antibody (Catalog # A13956-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC1 at approximately 59 kDa. The expected band size for LRRC1 is at 59 kDa. https://www.bosterbio.com/catalog/product/view/id/1260092026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19664-lrrc30-primary-antibodies-wb-testing-1.jpgAnti-LRRC30 Antibody Picoband® Western blot analysis of LRRC30 using anti-LRRC30 antibody (A19664). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC30 antigen affinity purified polyclonal antibody (Catalog # A19664) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LRRC30 at approximately 45 kDa. The expected band size for LRRC30 is at 34 kDa. https://www.bosterbio.com/catalog/product/view/id/1260102026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16326-1-lrrc40-primary-antibodies-wb-testing-1_1.jpgAnti-LRRC40 Antibody Picoband®Western blot analysis of LRRC40 using anti-LRRC40 antibody (A16326-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LRRC40 antigen affinity purified polyclonal antibody (Catalog # A16326-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LRRC40 at approximately 68 kDa. The expected band size for LRRC40 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16326-1-lrrc40-primary-antibodies-if-testing-1.jpgAnti-LRRC40 Antibody Picoband®IF analysis of LRRC40 using anti-LRRC40 antibody (A16326-1). LRRC40 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LRRC40 Antibody (A16326-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1260112026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17113-1-mcemp1-primary-antibodies-wb-testing-1.jpgAnti-MCEMP1 Antibody Picoband® Western blot analysis of MCEMP1 using anti-MCEMP1 antibody (A17113-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat lung tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCEMP1 antigen affinity purified polyclonal antibody (Catalog # A17113-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MCEMP1 at approximately 28 kDa. The expected band size for MCEMP1 is at 21 kDa. https://www.bosterbio.com/catalog/product/view/id/1260122026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00019-3-tgfb1-primary-antibodies-wb-testing-1.jpgAnti-TGFB1 Antibody Picoband® Western blot analysis of TGF Beta 1/TGFB1 using anti-TGF Beta 1/TGFB1 antibody (A00019-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TGF Beta 1/TGFB1 antigen affinity purified polyclonal antibody (Catalog # A00019-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TGF Beta 1/TGFB1 at approximately 44 kDa. The expected band size for TGF Beta 1/TGFB1 is at 44 kDa. https://www.bosterbio.com/catalog/product/view/id/1260132026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09345-2-mgarp-primary-antibodies-wb-testing-1.jpgAnti-MGARP Antibody Picoband® Western blot analysis of C4orf49/MGARP using anti-C4orf49/MGARP antibody (A09345-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A2780 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SK-OV-3 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C4orf49/MGARP antigen affinity purified polyclonal antibody (Catalog # A09345-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C4orf49/MGARP at approximately 38 kDa. The expected band size for C4orf49/MGARP is at 25 kDa. https://www.bosterbio.com/catalog/product/view/id/1260142026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00527-3-gli1-primary-antibodies-wb-testing-1.jpgAnti-GLI1 Antibody Picoband® Western blot analysis of GLI1 using anti-GLI1 antibody (A00527-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLI1 antigen affinity purified polyclonal antibody (Catalog # A00527-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLI1 at approximately 150 kDa. The expected band size for GLI1 is at 118 kDa. https://www.bosterbio.com/catalog/product/view/id/1260152026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14711-1-mmtag2-primary-antibodies-wb-testing-1.jpgAnti-MMTAG2 Antibody Picoband® Western blot analysis of C1orf35/MMTAG2 using anti-C1orf35/MMTAG2 antibody (A14711-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C1orf35/MMTAG2 antigen affinity purified polyclonal antibody (Catalog # A14711-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C1orf35/MMTAG2 at approximately 35 kDa. The expected band size for C1orf35/MMTAG2 is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14711-1-mmtag2-primary-antibodies-fcm-testing-2.pngAnti-MMTAG2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-C1orf35/MMTAG2 antibody (A14711-1). Overlay histogram showing MCF-7 cells stained with A14711-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-C1orf35/MMTAG2 Antibody (A14711-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260162026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04072-2-lims1-primary-antibodies-wb-testing-1.jpgAnti-LIMS1 Antibody Picoband® Western blot analysis of LIMS1 using anti-LIMS1 antibody (A04072-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse lung tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIMS1 antigen affinity purified polyclonal antibody (Catalog # A04072-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIMS1 at approximately 37 kDa. The expected band size for LIMS1 is at 37 kDa. https://www.bosterbio.com/catalog/product/view/id/1260172026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32724-lyz1-2-primary-antibodies-wb-testing-1.jpgAnti-Lyz1/2 Antibody Picoband® Western blot analysis of Lyz1/2 using anti-Lyz1/2 antibody (A32724). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lyz1/2 antigen affinity purified polyclonal antibody (Catalog # A32724) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lyz1/2 at approximately 14 kDa. The expected band size for Lyz1/2 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32724-lyz1-2-primary-antibodies-ihc-testing-2.jpgAnti-Lyz1/2 Antibody Picoband® IHC analysis of Lyz1/2 using anti-Lyz1/2 antibody (A32724). Lyz1/2 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lyz1/2 Antibody (A32724) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32724-lyz1-2-primary-antibodies-ihc-testing-3.jpgAnti-Lyz1/2 Antibody Picoband® IHC analysis of Lyz1/2 using anti-Lyz1/2 antibody (A32724). Lyz1/2 was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lyz1/2 Antibody (A32724) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32724-lyz1-2-primary-antibodies-ihc-testing-4.jpgAnti-Lyz1/2 Antibody Picoband® IHC analysis of Lyz1/2 using anti-Lyz1/2 antibody (A32724). Lyz1/2 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lyz1/2 Antibody (A32724) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32724-lyz1-2-primary-antibodies-ihc-testing-5.jpgAnti-Lyz1/2 Antibody Picoband® IHC analysis of Lyz1/2 using anti-Lyz1/2 antibody (A32724). Lyz1/2 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lyz1/2 Antibody (A32724) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32724-lyz1-2-primary-antibodies-ihc-testing-6.jpgAnti-Lyz1/2 Antibody Picoband® IHC analysis of Lyz1/2 using anti-Lyz1/2 antibody (A32724). Lyz1/2 was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lyz1/2 Antibody (A32724) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1260182026-03-17T05:16:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00756-4-ace2-primary-antibodies-wb-testing-1.jpgAnti-ACE2 Antibody Picoband® Western blot analysis of ACE2 using anti-ACE2 antibody (A00756-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human CCRF-CEM whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACE2 antigen affinity purified polyclonal antibody (Catalog # A00756-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACE2 at approximately 100 kDa. The expected band size for ACE2 is at 92 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00756-4-ace2-primary-antibodies-fcm-testing-2.pngAnti-ACE2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ACE2 antibody (A00756-4). Overlay histogram showing HepG2 cells stained with A00756-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ACE2 Antibody (A00756-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260192026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03186-2-pex19-primary-antibodies-wb-testing-1.jpgAnti-PEX19 Antibody Picoband® Western blot analysis of PEX19 using anti-PEX19 antibody (A03186-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PEX19 antigen affinity purified polyclonal antibody (Catalog # A03186-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PEX19 at approximately 38 kDa. The expected band size for PEX19 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03186-2-pex19-primary-antibodies-fcm-testing-2.pngAnti-PEX19 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PEX19 antibody (A03186-2). Overlay histogram showing JK cells stained with A03186-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PEX19 Antibody (A03186-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260202026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13748-1-pudp-primary-antibodies-wb-testing-1.jpgAnti-PUDP Antibody Picoband® Western blot analysis of PUDP using anti-PUDP antibody (A13748-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PUDP antigen affinity purified polyclonal antibody (Catalog # A13748-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PUDP at approximately 25 kDa. The expected band size for PUDP is at 25 kDa. https://www.bosterbio.com/catalog/product/view/id/1260212026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04458-1-galnt2-primary-antibodies-wb-testing-1.jpgAnti-GALNT2 Antibody Picoband® Western blot analysis of GALNT2 using anti-GALNT2 antibody (A04458-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MOLT-4 whole cell lysates, Lane 4: rat liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALNT2 antigen affinity purified polyclonal antibody (Catalog # A04458-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALNT2 at approximately 65 kDa. The expected band size for GALNT2 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04458-1-galnt2-primary-antibodies-if-testing-1.jpgAnti-GALNT2 Antibody Picoband®IF analysis of GALNT2 using anti-GALNT2 antibody (A04458-1) and anti-Alpha Tubulin antibody (M03989-3). GALNT2 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GALNT2 Antibody (A04458-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04458-1-galnt2-primary-antibodies-ip-testing-1.jpgAnti-GALNT2 Antibody Picoband®Immunoprecipitating (IP) GALNT2 in Hela whole cell lysate. Western blot analysis of GALNT2 using anti-GALNT2 antibody (A04458-1); Lane 1: Hela whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-GALNT2 antibody in Hela whole cell lysate; Lane 3: anti-GALNT2 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GALNT2 antigen affinity purified polyclonal antibody (A04458-1) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for GALNT2 at approximately 70 kDa. The expected band size for GALNT2 is at 65-70 kDa. https://www.bosterbio.com/catalog/product/view/id/1260222026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10021-1-galnt7-primary-antibodies-wb-testing-1_1.jpgAnti-GALNT7 Antibody Picoband®Western blot analysis of GALNT7 using anti-GALNT7 antibody (A10021-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALNT7 antigen affinity purified polyclonal antibody (A10021-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GALNT7 at approximately 75 kDa. The expected band size for GALNT7 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10021-1-galnt7-primary-antibodies-ihc-testing-1.jpgAnti-GALNT7 Antibody Picoband®IHC analysis of GALNT7 using anti-GALNT7 antibody (A10021-1). GALNT7 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GALNT7 Antibody (A10021-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10021-1-galnt7-primary-antibodies-ihc-testing-2.jpgAnti-GALNT7 Antibody Picoband®IHC analysis of GALNT7 using anti-GALNT7 antibody (A10021-1). GALNT7 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GALNT7 Antibody (A10021-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10021-1-galnt7-primary-antibodies-if-testing-1.jpgAnti-GALNT7 Antibody Picoband®IF analysis of GALNT7 using anti-GALNT7 antibody (A10021-1) and anti-Alpha Tubulin antibody (M03989-3). GALNT7 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GALNT7 Antibody (A10021-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10021-1-galnt7-primary-antibodies-if-testing-2.jpgAnti-GALNT7 Antibody Picoband®IF analysis of GALNT7 using anti-GALNT7 antibody (A10021-1). GALNT7 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-GALNT7 Antibody (A10021-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10021-1-galnt7-primary-antibodies-if-testing-3.jpgAnti-GALNT7 Antibody Picoband®IF analysis of GALNT7 using anti-GALNT7 antibody (A10021-1). GALNT7 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-GALNT7 Antibody (A10021-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10021-1-galnt7-primary-antibodies-ip-testing-1.jpgAnti-GALNT7 Antibody Picoband®Immunoprecipitating (IP) GALNT7 in Hacat whole cell lysate. Western blot analysis of GALNT7 using anti-GALNT7 antibody (A10021-1); Lane 1: Hacat whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-GALNT7 antibody in Hacat whole cell lysate; Lane 3: anti-GALNT7 antibody (2μg) + Hacat whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GALNT7 antigen affinity purified polyclonal antibody (A10021-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for GALNT7 at approximately 75 kDa. The expected band size for GALNT7 is at 75 kDa. https://www.bosterbio.com/catalog/product/view/id/1260232026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14343-1-galnt16-primary-antibodies-wb-testing-1.jpgAnti-GALNT16 Antibody Picoband® Western blot analysis of GALNT16 using anti-GALNT16 antibody (A14343-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALNT16 antigen affinity purified polyclonal antibody (Catalog # A14343-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALNT16 at approximately 70 kDa. The expected band size for GALNT16 is at 63 kDa. https://www.bosterbio.com/catalog/product/view/id/1260242026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15171-gas2l2-primary-antibodies-wb-testing-1.jpgAnti-GAS2L2 Antibody Picoband® Western blot analysis of GAS2L2 using anti-GAS2L2 antibody (A15171). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAS2L2 antigen affinity purified polyclonal antibody (Catalog # A15171) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAS2L2 at approximately 97 kDa. The expected band size for GAS2L2 is at 97 kDa. https://www.bosterbio.com/catalog/product/view/id/1260252026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06548-2-gas7-primary-antibodies-wb-testing-1.jpgAnti-GAS7 Antibody Picoband® Western blot analysis of GAS7 using anti-GAS7 antibody (A06548-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAS7 antigen affinity purified polyclonal antibody (Catalog # A06548-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAS7 at approximately 50 kDa. The expected band size for GAS7 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06548-2-gas7-primary-antibodies-fcm-testing-2.pngAnti-GAS7 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-GAS7 antibody (A06548-2). Overlay histogram showing JK cells stained with A06548-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GAS7 Antibody (A06548-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260262026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08058-1-gatb-primary-antibodies-wb-testing-1.jpgAnti-GATB Antibody Picoband® Western blot analysis of PET112/GATB using anti-PET112/GATB antibody (A08058-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PET112/GATB antigen affinity purified polyclonal antibody (Catalog # A08058-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PET112/GATB at approximately 62 kDa. The expected band size for PET112/GATB is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08058-1-gatb-primary-antibodies-fcm-testing-2.pngAnti-GATB Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PET112/GATB antibody (A08058-1). Overlay histogram showing JK cells stained with A08058-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PET112/GATB Antibody (A08058-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260272026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08549-2-gba-primary-antibodies-wb-testing-1.jpgAnti-GBA3 Antibody Picoband® Western blot analysis of GBA3 using anti-GBA3 antibody (A08549-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse liver tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GBA3 antigen affinity purified polyclonal antibody (Catalog # A08549-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GBA3 at approximately 50 kDa. The expected band size for GBA3 is at 54 kDa. https://www.bosterbio.com/catalog/product/view/id/1260282026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04694-1-gbe1-primary-antibodies-wb-testing-1.jpgAnti-GBE1 Antibody Picoband® Western blot analysis of GBE1 using anti-GBE1 antibody (A04694-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GBE1 antigen affinity purified polyclonal antibody (Catalog # A04694-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GBE1 at approximately 80 kDa. The expected band size for GBE1 is at 80 kDa. https://www.bosterbio.com/catalog/product/view/id/1260292026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-wb-testing-1.jpgAnti-RSRC2 Antibody Picoband® Western blot analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RSRC2 antigen affinity purified polyclonal antibody (Catalog # A13417-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RSRC2 at approximately 58 kDa. The expected band size for RSRC2 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-2.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-3.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-4.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human adrenocortical adenoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-5.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human adrenocortical adenoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-6.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-7.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-8.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human ovary serous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-9.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human ovary serous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-10.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-11.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-12.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-ihc-testing-13.jpgAnti-RSRC2 Antibody Picoband® IHC analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-if-testing-14.jpgAnti-RSRC2 Antibody Picoband® IF analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13417-1-rsrc2-primary-antibodies-if-testing-15.jpgAnti-RSRC2 Antibody Picoband® IF analysis of RSRC2 using anti-RSRC2 antibody (A13417-1). RSRC2 was detected in a paraffin-embedded section of human rectal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-RSRC2 Antibody (A13417-1) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1260302026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-wb-testing-1.jpgAnti-RLIM Antibody Picoband® Western blot analysis of RLIM using anti-RLIM antibody (A05428-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RLIM antigen affinity purified polyclonal antibody (Catalog # A05428-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RLIM at approximately 69 kDa. The expected band size for RLIM is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-2.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-3.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of diffuse large B-cell lymphoma of human intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-4.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-5.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-6.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-7.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-8.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-ihc-testing-9.jpgAnti-RLIM Antibody Picoband® IHC analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of human testicular seminoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-if-testing-10.jpgAnti-RLIM Antibody Picoband® IF analysis of RLIM using anti-RLIM antibody (A05428-1). RLIM was detected in a paraffin-embedded section of human esophageal squamous carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-RLIM Antibody (A05428-1) overnight at 4°C. DyLight®550 Conjugated Goat Anti-Rabbit IgG (BA1135) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05428-1-rlim-primary-antibodies-fcm-testing-11.pngAnti-RLIM Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-RLIM antibody (A05428-1). Overlay histogram showing Hela cells stained with A05428-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RLIM Antibody (A05428-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260332026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-wb-testing-1.jpgAnti-NRTN Antibody Picoband® Western blot analysis of NRTN using anti-NRTN antibody (A05924-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NRTN antigen affinity purified polyclonal antibody (Catalog # A05924-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NRTN at approximately 22 kDa. The expected band size for NRTN is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-2.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-3.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-4.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-5.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-6.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-7.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-8.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-9.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-10.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-11.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-12.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-13.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-14.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05924-3-nrtn-primary-antibodies-ihc-testing-15.jpgAnti-NRTN Antibody Picoband® IHC analysis of NRTN using anti-NRTN antibody (A05924-3). NRTN was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NRTN Antibody (A05924-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1260342026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04993-1-msl3-primary-antibodies-wb-testing-1.jpgAnti-MSL3 Antibody Picoband® Western blot analysis of MSL3 using anti-MSL3 antibody (A04993-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human CCRF-CEM whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MSL3 antigen affinity purified polyclonal antibody (Catalog # A04993-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MSL3 at approximately 70 kDa. The expected band size for MSL3 is at 60 kDa. https://www.bosterbio.com/catalog/product/view/id/1260372026-03-10T04:37:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2281.jpgMouse OSCAR ELISA Kit PicoKine®Mouse OSCAR ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1260382026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2282_2.pngHuman OSMRb ELISA Kit PicoKine®Human OSMRb ELISA Kit PicoKine standard curve https://www.bosterbio.com/products/human-ccl4-elisa-kit-ez-set-trade-diy-antibody-pairs-ez0450-boster.html2026-03-10T04:37:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0450.pngHuman CCL4 ELISA Kit EZ-Set™ (DIY Antibody Pairs)Human CCL4 EZ Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1260412026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-wb-testing-1.jpgAnti-C7orf30/MALSU1 Antibody Picoband® Western blot analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C7orf30/MALSU1 antigen affinity purified polyclonal antibody (Catalog # A12786) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for C7orf30/MALSU1 at approximately 24 kDa. The expected band size for C7orf30/MALSU1 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-2.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-3.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-4.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-5.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-6.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-7.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-8.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-9.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-10.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-ihc-testing-11.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IHC analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human prostate adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-fcm-testing-12.pngAnti-C7orf30/MALSU1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-C7orf30/MALSU1 antibody (A12786). Overlay histogram showing 293T cells stained with A12786 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-C7orf30/MALSU1 Antibody (A12786, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-fcm-testing-13.pngAnti-C7orf30/MALSU1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-C7orf30/MALSU1 antibody (A12786). Overlay histogram showing HepG2 cells stained with A12786 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-C7orf30/MALSU1 Antibody (A12786, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-if-testing-14.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IF analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12786-malsu1-primary-antibodies-if-testing-15.jpgAnti-C7orf30/MALSU1 Antibody Picoband® IF analysis of C7orf30/MALSU1 using anti-C7orf30/MALSU1 antibody (A12786). C7orf30/MALSU1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-C7orf30/MALSU1 Antibody (A12786) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1260422026-03-17T05:16:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04786-1-galp-primary-antibodies-wb-testing-1.jpgAnti-GALP Antibody Picoband® Western blot analysis of GALP using anti-GALP antibody (A04786-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human placenta tissue lysates, Lane 3: rat brain tissue lysates, Lane 4: rat liver tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALP antigen affinity purified polyclonal antibody (Catalog # A04786-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALP at approximately 15,18 kDa. The expected band size for GALP is at 13 kDa. https://www.bosterbio.com/catalog/product/view/id/1260432026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12630-1-garem1-primary-antibodies-wb-testing-1.jpgAnti-GAREM1 Antibody Picoband® Western blot analysis of GAREM1 using anti-GAREM1 antibody (A12630-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human SIHA whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GAREM1 antigen affinity purified polyclonal antibody (Catalog # A12630-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GAREM1 at approximately 97 kDa. The expected band size for GAREM1 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12630-1-garem1-primary-antibodies-ihc-testing-2.jpgAnti-GAREM1 Antibody Picoband® IHC analysis of GAREM1 using anti-GAREM1 antibody (A12630-1). GAREM1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GAREM1 Antibody (A12630-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12630-1-garem1-primary-antibodies-ihc-testing-3.jpgAnti-GAREM1 Antibody Picoband® IHC analysis of GAREM1 using anti-GAREM1 antibody (A12630-1). GAREM1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GAREM1 Antibody (A12630-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12630-1-garem1-primary-antibodies-fcm-testing-4.pngAnti-GAREM1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-GAREM1 antibody (A12630-1). Overlay histogram showing SH-SY5Y cells stained with A12630-11 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GAREM1 Antibody (A12630-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260442026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04618-2-gars-primary-antibodies-wb-testing-1.jpgAnti-GARS1 Antibody Picoband® Western blot analysis of GARS1 using anti-GARS1 antibody (A04618-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HT-1080 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GARS1 antigen affinity purified polyclonal antibody (Catalog # A04618-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GARS1 at approximately 80 kDa. The expected band size for GARS1 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04618-2-gars-primary-antibodies-fcm-testing-2..pngAnti-GARS1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GARS1 antibody (A04618-2). Overlay histogram showing HepG2 cells stained with A04618-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GARS1 Antibody (A04618-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260452026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-wb-testing-1.jpgAnti-Vaspin/SERPINA12 Antibody Picoband® Western blot analysis of Vaspin/SERPINA12 using anti-Vaspin/SERPINA12 antibody (A05352-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse B16-F10 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Vaspin/SERPINA12 antigen affinity purified polyclonal antibody (Catalog # A05352-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Vaspin/SERPINA12 at approximately 55 kDa. The expected band size for Vaspin/SERPINA12 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-ihc-testing-6.jpgAnti-Vaspin/SERPINA12 Antibody Picoband®IHC analysis of Vaspin/SERPINA12 using anti-Vaspin/SERPINA12 antibody (A05352-2). Vaspin/SERPINA12 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Vaspin/SERPINA12 Antibody (A05352-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-ihc-testing-7.jpgAnti-Vaspin/SERPINA12 Antibody Picoband®IHC analysis of Vaspin/SERPINA12 using anti-Vaspin/SERPINA12 antibody (A05352-2). Vaspin/SERPINA12 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Vaspin/SERPINA12 Antibody (A05352-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-ihc-testing-2.jpgAnti-Vaspin/SERPINA12 Antibody Picoband® IHC analysis of Vaspin/SERPINA12 using anti-Vaspin/SERPINA12 antibody (A05352-2). Vaspin/SERPINA12 was detected in a paraffin-embedded section of adipose of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Vaspin/SERPINA12 Antibody (A05352-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-ihc-testing-3.jpgAnti-Vaspin/SERPINA12 Antibody Picoband® IHC analysis of Vaspin/SERPINA12 using anti-Vaspin/SERPINA12 antibody (A05352-2). Vaspin/SERPINA12 was detected in a paraffin-embedded section of adipose of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Vaspin/SERPINA12 Antibody (A05352-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-ihc-testing-4.jpgAnti-Vaspin/SERPINA12 Antibody Picoband® IHC analysis of Vaspin/SERPINA12 using anti-Vaspin/SERPINA12 antibody (A05352-2). Vaspin/SERPINA12 was detected in a paraffin-embedded section of adipose of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Vaspin/SERPINA12 Antibody (A05352-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-ihc-testing-5.jpgAnti-Vaspin/SERPINA12 Antibody Picoband® IHC analysis of Vaspin/SERPINA12 using anti-Vaspin/SERPINA12 antibody (A05352-2). Vaspin/SERPINA12 was detected in a paraffin-embedded section of adipose of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Vaspin/SERPINA12 Antibody (A05352-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05352-2-serpina12-primary-antibodies-fcm-testing-6.pngAnti-Vaspin/SERPINA12 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Vaspin/SERPINA12 antibody (A05352-2). Overlay histogram showing HepG2 cells stained with A05352-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Vaspin/SERPINA12 Antibody (A05352-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260462026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12693-3-lgals7-primary-antibodies-wb-testing-1.jpgAnti-Galectin-7/LGALS7 Antibody Picoband® Western blot analysis of Galectin-7/LGALS7 using anti-Galectin-7/LGALS7 antibody (A12693-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skin tissue lysates, Lane 2: mouse skin tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Galectin-7/LGALS7 antigen affinity purified polyclonal antibody (Catalog # A12693-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Galectin-7/LGALS7 at approximately 15 kDa. The expected band size for Galectin-7/LGALS7 is at 15 kDa. https://www.bosterbio.com/catalog/product/view/id/1260472026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11132-1-lsm11-primary-antibodies-wb-testing-1.jpgAnti-LSM11 Antibody Picoband® Western blot analysis of LSM11 using anti-LSM11 antibody (A11132-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: rat skin tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LSM11 antigen affinity purified polyclonal antibody (Catalog # A11132-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LSM11 at approximately 68 kDa. The expected band size for LSM11 is at 40 kDa. https://www.bosterbio.com/catalog/product/view/id/1260482026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09433-3-idh3b-primary-antibodies-wb-testing-1.jpgAnti-IDH3B Antibody Picoband® Western blot analysis of IDH3B using anti-IDH3B antibody (A09433-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human LANAP whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDH3B antigen affinity purified polyclonal antibody (Catalog # A09433-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDH3B at approximately 42 kDa. The expected band size for IDH3B is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09433-3-idh3b-primary-antibodies-ihc-testing-2.jpgAnti-IDH3B Antibody Picoband® IHC analysis of IDH3B using anti-IDH3B antibody (A09433-3). IDH3B was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3B Antibody (A09433-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09433-3-idh3b-primary-antibodies-ihc-testing-3.jpgAnti-IDH3B Antibody Picoband® IHC analysis of IDH3B using anti-IDH3B antibody (A09433-3). IDH3B was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3B Antibody (A09433-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09433-3-idh3b-primary-antibodies-ihc-testing-4.jpgAnti-IDH3B Antibody Picoband® IHC analysis of IDH3B using anti-IDH3B antibody (A09433-3). IDH3B was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3B Antibody (A09433-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09433-3-idh3b-primary-antibodies-ihc-testing-5.jpgAnti-IDH3B Antibody Picoband® IHC analysis of IDH3B using anti-IDH3B antibody (A09433-3). IDH3B was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IDH3B Antibody (A09433-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09433-3-idh3b-primary-antibodies-fcm-testing-6_1.pngAnti-IDH3B Antibody Picoband® Flow Cytometry analysis of JK cells using anti-IDH3B antibody (A09433-3). Overlay histogram showing JK cells stained with A09433-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IDH3B Antibody (A09433-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09433-3-idh3b-primary-antibodies-ip-testing-7.jpgAnti-IDH3B Antibody Picoband® Immunoprecipitating IDH3B in U251 whole cell lysate. Western blot analysis of IDH3B using anti-IDH3B antibody (A09433-3). Lane 1: U251 whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-IDH3B antibody in U251 whole cell lysate. Lane 3: anti-IDH3B antibody (2μg) + U251 whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IDH3B antigen affinity purified polyclonal antibody (A09433-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for IDH3B at approximately 42 kDa. The expected band size for IDH3B is at 42 kDa. https://www.bosterbio.com/catalog/product/view/id/1260492026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09946-galnt12-primary-antibodies-wb-testing-1.jpgAnti-GALNT12 Antibody Picoband® Western blot analysis of GALNT12 using anti-GALNT12 antibody (A09946). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALNT12 antigen affinity purified polyclonal antibody (Catalog # A09946) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALNT12 at approximately 67 kDa. The expected band size for GALNT12 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09946-galnt12-primary-antibodies-if-testing-2.jpgAnti-GALNT12 Antibody Picoband® IF analysis of GALNT12 using anti-GALNT12 antibody (A09946) and anti-Beta Tubulin antibody (M01857-3). GALNT12 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GALNT12 Antibody (A09946) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09946-galnt12-primary-antibodies-fcm-testing-3.pngAnti-GALNT12 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-GALNT12 antibody (A09946). Overlay histogram showing A549 cells stained with A09946 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GALNT12 Antibody (A09946, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260502026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06061-2-gart-primary-antibodies-wb-testing-1.jpgAnti-GART Antibody Picoband® Western blot analysis of GART using anti-GART antibody (A06061-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GART antigen affinity purified polyclonal antibody (Catalog # A06061-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GART at approximately 108 kDa. The expected band size for GART is at 108 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06061-2-gart-primary-antibodies-fcm-testing-2.pngAnti-GART Antibody Picoband® Flow Cytometry analysis of HELA cells using anti-GART antibody (A06061-2). Overlay histogram showing HELA cells stained with A06061-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GART Antibody (A06061-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06061-2-gart-primary-antibodies-fcm-testing-3.pngAnti-GART Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GART antibody (A06061-2). Overlay histogram showing HepG2 cells stained with A06061-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GART Antibody (A06061-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260512026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12257-2-phkg1-primary-antibodies-wb-testing-1.jpgAnti-PHKG1 Antibody Picoband® Western blot analysis of PHKG1 using anti-PHKG1 antibody (A12257-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHKG1 antigen affinity purified polyclonal antibody (Catalog # A12257-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHKG1 at approximately 40 kDa. The expected band size for PHKG1 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12257-2-phkg1-primary-antibodies-fcm-testing-2.pngAnti-PHKG1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PHKG1 antibody (A12257-2). Overlay histogram showing JK cells stained with A12257-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHKG1 Antibody (A12257-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260522026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-wb-testing-1.jpgAnti-FAM111B Antibody Picoband® Western blot analysis of FAM111B using anti-FAM111B antibody (A14246-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAM111B antigen affinity purified polyclonal antibody (Catalog # A14246-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FAM111B at approximately 85 kDa. The expected band size for FAM111B is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-wb-testing-2.jpgAnti-FAM111B Antibody Picoband® Western blot analysis of FAM111B using anti-FAM111B antibody (A14246-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAM111B antigen affinity purified polyclonal antibody (Catalog # A14246-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FAM111B at approximately 85 kDa. The expected band size for FAM111B is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-ihc-testing-3.jpgAnti-FAM111B Antibody Picoband® IHC analysis of FAM111B using anti-FAM111B antibody (A14246-2). FAM111B was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM111B Antibody (A14246-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-ihc-testing-4.jpgAnti-FAM111B Antibody Picoband® IHC analysis of FAM111B using anti-FAM111B antibody (A14246-2). FAM111B was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM111B Antibody (A14246-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-ihc-testing-5.jpgAnti-FAM111B Antibody Picoband® IHC analysis of FAM111B using anti-FAM111B antibody (A14246-2). FAM111B was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM111B Antibody (A14246-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-ihc-testing-6.jpgAnti-FAM111B Antibody Picoband® IHC analysis of FAM111B using anti-FAM111B antibody (A14246-2). FAM111B was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM111B Antibody (A14246-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-ihc-testing-7.jpgAnti-FAM111B Antibody Picoband® IHC analysis of FAM111B using anti-FAM111B antibody (A14246-2). FAM111B was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM111B Antibody (A14246-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-ihc-testing-8.jpgAnti-FAM111B Antibody Picoband® IHC analysis of FAM111B using anti-FAM111B antibody (A14246-2). FAM111B was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM111B Antibody (A14246-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14246-2-fam111b-primary-antibodies-fcm-testing-9.pngAnti-FAM111B Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-FAM111B antibody (A14246-2). Overlay histogram showing MCF-7 cells stained with A14246-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FAM111B Antibody (A14246-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260532026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03010-1-drd5-primary-antibodies-wb-testing-1.jpgAnti-DRD5 Antibody Picoband® Western blot analysis of DRD5 using anti-DRD5 antibody (A03010-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DRD5 antigen affinity purified polyclonal antibody (Catalog # A03010-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DRD5 at approximately 58 kDa. The expected band size for DRD5 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03010-1-drd5-primary-antibodies-fcm-testing-2.pngAnti-DRD5 Antibody Picoband® Flow Cytometry analysis of U937 cells using anti-DRD5 antibody (A03010-1). Overlay histogram showing U937 cells stained with A03010-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-DRD5 Antibody (A03010-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260542026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01247-4-irak4-primary-antibodies-wb-testing-1.jpgAnti-IRAK4 Antibody Picoband® Western blot analysis of IRAK4 using anti-IRAK4 antibody (A01247-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRAK4 antigen affinity purified polyclonal antibody (Catalog # A01247-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRAK4 at approximately 52 kDa. The expected band size for IRAK4 is at 52 kDa. https://www.bosterbio.com/catalog/product/view/id/1260552026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-wb-testing-1.jpgAnti-MYH14 Antibody Picoband® Western blot analysis of MYH14 using anti-MYH14 antibody (A04528-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human U-87MG whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: rat lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYH14 antigen affinity purified polyclonal antibody (Catalog # A04528-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYH14 at approximately 250 kDa. The expected band size for MYH14 is at 228 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-2.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-3.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-4.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-5.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-6.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-7.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-8.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-ihc-testing-9.jpgAnti-MYH14 Antibody Picoband® IHC analysis of MYH14 using anti-MYH14 antibody (A04528-3). MYH14 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MYH14 Antibody (A04528-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04528-3-myh14-primary-antibodies-fcm-testing-10.pngAnti-MYH14 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MYH14 antibody (A04528-3). Overlay histogram showing HepG2 cells stained with A04528-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYH14 Antibody (A04528-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260562026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04016-2-gga2-primary-antibodies-wb-testing-1.jpgAnti-GGA2 Antibody Picoband® Western blot analysis of GGA2 using anti-GGA2 antibody (A04016-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GGA2 antigen affinity purified polyclonal antibody (Catalog # A04016-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GGA2 at approximately 70 kDa. The expected band size for GGA2 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04016-2-gga2-primary-antibodies-fcm-testing-2.pngAnti-GGA2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GGA2 antibody (A04016-2). Overlay histogram showing HepG2 cells stained with A04016-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GGA2 Antibody (A04016-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04016-2-gga2-primary-antibodies-ip-testing-3.jpgAnti-GGA2 Antibody Picoband® Immunoprecipitating GGA2 in HepG2 whole cell lysate. Western blot analysis of GGA2 using anti-GGA2 antibody (A04016-2); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-GGA2 antibody in HepG2 whole cell lysate; Lane 3: anti-GGA2 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GGA2 antigen affinity purified polyclonal antibody (A04016-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for GGA2 at approximately 70 kDa. The expected band size for GGA2 is at 67 kDa. https://www.bosterbio.com/catalog/product/view/id/1260572026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00986-3-axin1-primary-antibodies-wb-testing-1.jpgAnti-AXIN1 Antibody Picoband® Western blot analysis of AXIN1 using anti-AXIN1 antibody (A00986-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AXIN1 antigen affinity purified polyclonal antibody (Catalog # A00986-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AXIN1 at approximately 110 kDa. The expected band size for AXIN1 is at 96 kDa. https://www.bosterbio.com/catalog/product/view/id/1260582026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05300-1-clcn3-primary-antibodies-wb-testing-1.jpgAnti-CLCN3 Antibody Picoband® Western blot analysis of CLCN3 using anti-CLCN3 antibody (A05300-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human U-87MG whole cell lysates, Lane 3: human SH-SY6Y whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: human A549 whole cell lysates, Lane 6: human Hela whole cell lysates, Lane 7: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLCN3 antigen affinity purified polyclonal antibody (Catalog # A05300-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CLCN3 at approximately 170 kDa. The expected band size for CLCN3 is at 91 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05300-1-clcn3-primary-antibodies-ihc-testing-2.jpgAnti-CLCN3 Antibody Picoband® IHC analysis of CLCN3 using anti-CLCN3 antibody (A05300-1). CLCN3 was detected in a paraffin-embedded section of human prostatic cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLCN3 Antibody (A05300-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05300-1-clcn3-primary-antibodies-ihc-testing-3.jpgAnti-CLCN3 Antibody Picoband® IHC analysis of CLCN3 using anti-CLCN3 antibody (A05300-1). CLCN3 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLCN3 Antibody (A05300-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05300-1-clcn3-primary-antibodies-if-testing-4.jpgAnti-CLCN3 Antibody Picoband® IF analysis of CLCN3 using anti-CLCN3 antibody (A05300-1). CLCN3 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CLCN3 Antibody (A05300-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05300-1-clcn3-primary-antibodies-fcm-testing-5.jpgAnti-CLCN3 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-AXIN1 antibody (A05300-1). Overlay histogram showing JK cells stained with A05300-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-AXIN1 Antibody (A05300-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1260592026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13669-snx25-primary-antibodies-wb-testing-1.jpgAnti-SNX25 Antibody Picoband® Western blot analysis of SNX25 using anti-SNX25 antibody (A13669). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat thymus tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SNX25 antigen affinity purified polyclonal antibody (Catalog # A13669) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SNX25 at approximately 100 kDa. The expected band size for SNX25 is at 98 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13669-snx25-primary-antibodies-fcm-testing-2.pngAnti-SNX25 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-SNX25 antibody (A13669). Overlay histogram showing HepG2 cells stained with A13669 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SNX25 Antibody (A13669, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260602026-03-17T05:16:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10839-man2c1-primary-antibodies-wb-testing-1.jpgAnti-MAN2C1 Antibody Picoband® Western blot analysis of MAN2C1 using anti-MAN2C1 antibody (A10839). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAN2C1 antigen affinity purified polyclonal antibody (Catalog # A10839) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAN2C1 at approximately 100 kDa. The expected band size for MAN2C1 is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10839-man2c1-primary-antibodies-if-testing-2.jpgAnti-MAN2C1 Antibody Picoband® IF analysis of MAN2C1 using anti-MAN2C1 antibody (A10839) and anti-Beta Tubulin antibody (M01857-3). MAN2C1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAN2C1 Antibody (A10839) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10839-man2c1-primary-antibodies-fcm-testing-3.pngAnti-MAN2C1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-MAN2C1 antibody (A10839). Overlay histogram showing JK cells stained with A10839 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAN2C1 Antibody (A10839, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260612026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04567-4-mastl-primary-antibodies-wb-testing-1.jpgAnti-MASTL Antibody Picoband® Western blot analysis of MASTL using anti-MASTL antibody (A04567-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MASTL antigen affinity purified polyclonal antibody (Catalog # A04567-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MASTL at approximately 110 kDa. The expected band size for MASTL is at 96 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04567-4-mastl-primary-antibodies-wb-testing-2.jpgAnti-MASTL Antibody Picoband® Western blot analysis of MASTL using anti-MASTL antibody (A04567-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U2OS whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SIHA whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MASTL antigen affinity purified polyclonal antibody (Catalog # A04567-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MASTL at approximately 110 kDa. The expected band size for MASTL is at 96 kDa. https://www.bosterbio.com/catalog/product/view/id/1260622026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32480-myorg-primary-antibodies-wb-testing-1.jpgAnti-MYORG Antibody Picoband® Western blot analysis of MYORG using anti-MYORG antibody (A32480). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat ovary tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse ovary tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYORG antigen affinity purified polyclonal antibody (Catalog # A32480) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYORG at approximately 87 kDa. The expected band size for MYORG is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32480-myorg-primary-antibodies-fcm-testing-2.pngAnti-MYORG Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-MYORG antibody (A32480). Overlay histogram showing HepG2 cells stained with A32480 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYORG Antibody (A32480, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260632026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15308-2-idnk-primary-antibodies-wb-testing-1.jpgAnti-IDNK Antibody Picoband® Western blot analysis of IDNK using anti-IDNK antibody (A15308-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat kisney tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IDNK antigen affinity purified polyclonal antibody (Catalog # A15308-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IDNK at approximately 21 kDa. The expected band size for IDNK is at 21 kDa. https://www.bosterbio.com/catalog/product/view/id/1260642026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16075-1-igfl3-primary-antibodies-wb-testing-1.jpgAnti-IGFL3 Antibody Picoband® Western blot analysis of IGFL3 using anti-IGFL3 antibody (A16075-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGFL3 antigen affinity purified polyclonal antibody (Catalog # A16075-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGFL3 at approximately 18 kDa. The expected band size for IGFL3 is at 14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16075-1-igfl3-primary-antibodies-ihc-testing-2.jpgAnti-IGFL3 Antibody Picoband® IHC analysis of IGFL3 using anti-IGFL3 antibody (A16075-1). IGFL3 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGFL3 Antibody (A16075-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16075-1-igfl3-primary-antibodies-ihc-testing-3.jpgAnti-IGFL3 Antibody Picoband® IHC analysis of IGFL3 using anti-IGFL3 antibody (A16075-1). IGFL3 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGFL3 Antibody (A16075-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16075-1-igfl3-primary-antibodies-ihc-testing-4.jpgAnti-IGFL3 Antibody Picoband® IHC analysis of IGFL3 using anti-IGFL3 antibody (A16075-1). IGFL3 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGFL3 Antibody (A16075-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16075-1-igfl3-primary-antibodies-ihc-testing-5.jpgAnti-IGFL3 Antibody Picoband® IHC analysis of IGFL3 using anti-IGFL3 antibody (A16075-1). IGFL3 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IGFL3 Antibody (A16075-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1260652026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32411-inava-primary-antibodies-wb-testing-1.jpgAnti-INAVA Antibody Picoband® Western blot analysis of INAVA using anti-INAVA antibody (A32411). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INAVA antigen affinity purified polyclonal antibody (Catalog # A32411) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INAVA at approximately 70 kDa. The expected band size for INAVA is at 73 kDa. https://www.bosterbio.com/catalog/product/view/id/1260662026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14973-1-insm2-primary-antibodies-wb-testing-1.jpgAnti-INSM2 Antibody Picoband® Western blot analysis of INSM2 using anti-INSM2 antibody (A14973-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INSM2 antigen affinity purified polyclonal antibody (Catalog # A14973-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INSM2 at approximately 59 kDa. The expected band size for INSM2 is at 59 kDa. https://www.bosterbio.com/catalog/product/view/id/1260672026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13989-1-iqce-primary-antibodies-wb-testing-1.jpgAnti-IQCE Antibody Picoband® Western blot analysis of IQCE using anti-IQCE antibody (A13989-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IQCE antigen affinity purified polyclonal antibody (Catalog # A13989-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IQCE at approximately 72 kDa. The expected band size for IQCE is at 77 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13989-1-iqce-primary-antibodies-if-testing-2.jpgAnti-IQCE Antibody Picoband® IF analysis of IQCE using anti-IQCE antibody (A13989-1) and anti-Beta Tubulin antibody (M01857-3). IQCE was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IQCE Antibody (A13989-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Donkey Anti-Rabbit IgG and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1260682026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00070-3-igf1r-primary-antibodies-wb-testing-1.jpgAnti-IGF1R Antibody Picoband® Western blot analysis of IGF1R using anti-IGF1R antibody (A00070-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IGF1R antigen affinity purified polyclonal antibody (Catalog # A00070-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IGF1R at approximately 110,200 kDa. The expected band size for IGF1R is at 155 kDa. https://www.bosterbio.com/catalog/product/view/id/1260692026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12583-1-colgalt1-primary-antibodies-wb-testing-1.jpgAnti-GLT25D1/COLGALT1 Antibody Picoband® Western blot analysis of GLT25D1/COLGALT1 using anti-GLT25D1/COLGALT1 antibody (A12583-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLT25D1/COLGALT1 antigen affinity purified polyclonal antibody (Catalog # A12583-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLT25D1/COLGALT1 at approximately 85 kDa. The expected band size for GLT25D1/COLGALT1 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12583-1-colgalt1-primary-antibodies-fcm-testing-2.pngAnti-GLT25D1/COLGALT1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-GLT25D1/COLGALT1 antibody (A12583-1). Overlay histogram showing HEL cells stained with A12583-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLT25D1/COLGALT1 Antibody (A12583-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260702026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-wb-testing-1.jpgAnti-IRF2BP1 Antibody Picoband® Western blot analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRF2BP1 antigen affinity purified polyclonal antibody (Catalog # A11406-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRF2BP1 at approximately 72 kDa. The expected band size for IRF2BP1 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-2.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-3.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human acinic cell carcinoma of parotid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-4.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-5.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-6.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human clear cell renal carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-7.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human clear cell renal carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-8.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-9.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-10.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-11.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-12.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-13.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-14.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-15.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-16.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-17.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-18.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-19.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-20.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-21.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-22.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ihc-testing-23.jpgAnti-IRF2BP1 Antibody Picoband® IHC analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-if-testing-24.jpgAnti-IRF2BP1 Antibody Picoband® IF analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2). IRF2BP1 was detected in an immunocytochemical section of TPC1 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IRF2BP1 Antibody (A11406-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-fcm-testing-25.pngAnti-IRF2BP1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-IRF2BP1 antibody (A11406-2). Overlay histogram showing HEL cells stained with A11406-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IRF2BP1 Antibody (A11406-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11406-2-irf2bp1-primary-antibodies-ip-testing-26.jpgAnti-IRF2BP1 Antibody Picoband® Immunoprecipitating IRF2BP1 in HepG2 whole cell lysate. Western blot analysis of IRF2BP1 using anti-IRF2BP1 antibody (A11406-2); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-IRF2BP1 antibody in HepG2 whole cell lysate; Lane 3: anti-IRF2BP1 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-IRF2BP1 antigen affinity purified polyclonal antibody (A11406-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for IRF2BP1 at approximately 72 kDa. The expected band size for IRF2BP1 is at 62 kDa. https://www.bosterbio.com/catalog/product/view/id/1260712026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-wb-testing-1.jpgAnti-IRF2BPL Antibody Picoband® Western blot analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human MCF-7whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRF2BPL antigen affinity purified polyclonal antibody (Catalog # A10706) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRF2BPL at approximately 95 kDa. The expected band size for IRF2BPL is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-ihc-testing-2.jpgAnti-IRF2BPL Antibody Picoband® IHC analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). IRF2BPL was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BPL Antibody (A10706) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-ihc-testing-3.jpgAnti-IRF2BPL Antibody Picoband® IHC analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). IRF2BPL was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BPL Antibody (A10706) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-ihc-testing-4.jpgAnti-IRF2BPL Antibody Picoband® IHC analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). IRF2BPL was detected in a paraffin-embedded section of follicles of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BPL Antibody (A10706) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-ihc-testing-5.jpgAnti-IRF2BPL Antibody Picoband® IHC analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). IRF2BPL was detected in a paraffin-embedded section of follicles of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BPL Antibody (A10706) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-ihc-testing-6.jpgAnti-IRF2BPL Antibody Picoband® IHC analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). IRF2BPL was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BPL Antibody (A10706) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-ihc-testing-7.jpgAnti-IRF2BPL Antibody Picoband® IHC analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). IRF2BPL was detected in a paraffin-embedded section of follicles of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IRF2BPL Antibody (A10706) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-if-testing-8.jpgAnti-IRF2BPL Antibody Picoband® IF analysis of IRF2BPL using anti-IRF2BPL antibody (A10706). IRF2BPL was detected in an immunocytochemical section of TPC1 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IRF2BPL Antibody (A10706) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10706-irf2bpl-primary-antibodies-fcm-testing-9.jpgAnti-IRF2BPL Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-IRF2BPL antibody (A10706). Overlay histogram showing HEL cells stained with A10706 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IRF2BPL Antibody (A10706, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1260722026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09571-2-scara5-primary-antibodies-wb-testing-1.jpgAnti-SCARA5 Antibody Picoband® Western blot analysis of SCARA5 using anti-SCARA5 antibody (A09571-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCARA5 antigen affinity purified polyclonal antibody (Catalog # A09571-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SCARA5 at approximately 50 kDa. The expected band size for SCARA5 is at 54 kDa. https://www.bosterbio.com/catalog/product/view/id/1260732026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04954-1-inpp5f-primary-antibodies-wb-testing-1.jpgAnti-INPP5F Antibody Picoband® Western blot analysis of INPP5F using anti-INPP5F antibody (A04954-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-INPP5F antigen affinity purified polyclonal antibody (Catalog # A04954-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for INPP5F at approximately 128 kDa. The expected band size for INPP5F is at 128 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04954-1-inpp5f-primary-antibodies-fcm-testing-2.pngAnti-INPP5F Antibody Picoband® Flow Cytometry analysis of Daudi cells using anti-INPP5F antibody (A04954-1). Overlay histogram showing Daudi cells stained with A04954-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-INPP5F Antibody (A04954-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260742026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04954-1-irgq-primary-antibodies-wb-testing-1.jpgAnti-IRGQ Antibody Picoband® Western blot analysis of IRGQ using anti-IRGQ antibody (A17389-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A2780 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRGQ antigen affinity purified polyclonal antibody (Catalog # A17389-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRGQ at approximately 68 kDa. The expected band size for IRGQ is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04954-1-irgq-primary-antibodies-fcm-testing-2.pngAnti-IRGQ Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-IRGQ antibody (A17389-1). Overlay histogram showing HEL cells stained with A17389-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IRGQ Antibody (A17389-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260752026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12588-2-irx1-primary-antibodies-wb-testing-1.jpgAnti-IRX1 Antibody Picoband® Western blot analysis of IRX1 using anti-IRX1 antibody (A12588-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: rat lung tissue lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse lung tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse LLC tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IRX1 antigen affinity purified polyclonal antibody (Catalog # A12588-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IRX1 at approximately 50 kDa. The expected band size for IRX1 is at 50 kDa. https://www.bosterbio.com/catalog/product/view/id/1260762026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00177-3-sox9-primary-antibodies-wb-testing-1.jpgAnti-SOX9 Antibody Picoband® Western blot analysis of SOX9 using anti-SOX9 antibody (A00177-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOX9 antigen affinity purified polyclonal antibody (Catalog # A00177-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOX9 at approximately 75 kDa. The expected band size for SOX9 is at 56 kDa. https://www.bosterbio.com/catalog/product/view/id/1260772026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02969-4-isl1-primary-antibodies-wb-testing-1.jpgAnti-Islet 1/ISL1 Antibody Picoband® Western blot analysis of Islet 1/ISL1 using anti-Islet 1/ISL1 antibody (A02969-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SIHA whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Islet 1/ISL1 antigen affinity purified polyclonal antibody (Catalog # A02969-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Islet 1/ISL1 at approximately 50 kDa. The expected band size for Islet 1/ISL1 is at 39 kDa. https://www.bosterbio.com/catalog/product/view/id/1260782026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08760-3-hibadh-primary-antibodies-wb-testing-1.jpgAnti-HIBADH Antibody Picoband® Western blot analysis of HIBADH using anti-HIBADH antibody (A08760-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat NRK whole cell lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HIBADH antigen affinity purified polyclonal antibody (Catalog # A08760-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HIBADH at approximately 32 kDa. The expected band size for HIBADH is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08760-3-hibadh-primary-antibodies-fcm-testing-2.pngAnti-HIBADH Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-HIBADH antibody (A08760-3). Overlay histogram showing A549 cells stained with A08760-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HIBADH Antibody (A08760-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260792026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-wb-testing-1.jpgAnti-HTATSF1 Antibody Picoband® Western blot analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HTATSF1 antigen affinity purified polyclonal antibody (Catalog # A07890-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HTATSF1 at approximately 140 kDa. The expected band size for HTATSF1 is at 86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-2.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-3.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-4.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-5.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-6.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-7.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-8.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-9.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-10.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-11.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-12.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-ihc-testing-13.jpgAnti-HTATSF1 Antibody Picoband® IHC analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-fcm-testing-14.pngAnti-HTATSF1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-HTATSF1 antibody (A07890-2). Overlay histogram showing MCF-7 cells stained with A07890-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HTATSF1 Antibody (A07890-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-if-testing-15.jpgAnti-HTATSF1 Antibody Picoband® IF analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07890-2-htatsf1-primary-antibodies-if-testing-16.jpgAnti-HTATSF1 Antibody Picoband® IF analysis of HTATSF1 using anti-HTATSF1 antibody (A07890-2). HTATSF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HTATSF1 Antibody (A07890-2) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1260802026-03-17T05:16:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14181-1-isoc2-primary-antibodies-wb-testing-1.jpgAnti-ISOC2 Antibody Picoband® Western blot analysis of ISOC2 using anti-ISOC2 antibody (A14181-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human LNCAP whole cell lysates, Lane 2: human PANC-1 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ISOC2 antigen affinity purified polyclonal antibody (Catalog # A14181-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ISOC2 at approximately 22 kDa. The expected band size for ISOC2 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14181-1-isoc2-primary-antibodies-if-testing-2.jpgAnti-ISOC2 Antibody Picoband® IF analysis of ISOC2 using anti-ISOC2 antibody (A14181-1). ISOC2 was detected in an immunocytochemical section of BEAS-2B cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ISOC2 Antibody (A14181-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1260812026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13079-1-htra4-primary-antibodies-wb-testing-1.jpgAnti-HTRA4 Antibody Picoband® Western blot analysis of HTRA4 using anti-HTRA4 antibody (A13079-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HTRA4 antigen affinity purified polyclonal antibody (Catalog # A13079-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HTRA4 at approximately 51 kDa. The expected band size for HTRA4 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13079-1-htra4-primary-antibodies-fcm-testing-2.pngAnti-HTRA4 Antibody Picoband® Flow Cytometry analysis of Daudi cells using anti-HTRA4 antibody (A13079-1). Overlay histogram showing Daudi cells stained with A13079-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-HTRA4 Antibody (A13079-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260822026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02318-2-pgm1-primary-antibodies-wb-testing-1.jpgAnti-PGM1 Antibody Picoband® Western blot analysis of PGM1 using anti-PGM1 antibody (A02318-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: rat skin tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse skin tissue lysates, Lane 7: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGM1 antigen affinity purified polyclonal antibody (Catalog # A02318-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PGM1 at approximately 64 kDa. The expected band size for PGM1 is at 61 kDa. https://www.bosterbio.com/catalog/product/view/id/1260832026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10475-2-pipox-primary-antibodies-wb-testing-1.jpgAnti-PIPOX Antibody Picoband® Western blot analysis of PIPOX using anti-PIPOX antibody (A10475-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIPOX antigen affinity purified polyclonal antibody (Catalog # A10475-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PIPOX at approximately 40 kDa. The expected band size for PIPOX is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10475-2-pipox-primary-antibodies-ihc-testing-2.jpgAnti-PIPOX Antibody Picoband® IHC analysis of PIPOX using anti-PIPOX antibody (A10475-2). PIPOX was detected in a paraffin-embedded section of human ovary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIPOX Antibody (A10475-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10475-2-pipox-primary-antibodies-ihc-testing-3.jpgAnti-PIPOX Antibody Picoband® IHC analysis of PIPOX using anti-PIPOX antibody (A10475-2). PIPOX was detected in a paraffin-embedded section of human ovary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIPOX Antibody (A10475-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10475-2-pipox-primary-antibodies-ihc-testing-4.jpgAnti-PIPOX Antibody Picoband® IHC analysis of PIPOX using anti-PIPOX antibody (A10475-2). PIPOX was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIPOX Antibody (A10475-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10475-2-pipox-primary-antibodies-ihc-testing-5.jpgAnti-PIPOX Antibody Picoband® IHC analysis of PIPOX using anti-PIPOX antibody (A10475-2). PIPOX was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIPOX Antibody (A10475-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1260842026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11987-1-pomgnt2-primary-antibodies-wb-testing-1.jpgAnti-POMGNT2 Antibody Picoband® Western blot analysis of POMGNT2 using anti-POMGNT2 antibody (A11987-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human U2OS whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POMGNT2 antigen affinity purified polyclonal antibody (Catalog # A11987-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POMGNT2 at approximately 75 kDa. The expected band size for POMGNT2 is at 67 kDa. https://www.bosterbio.com/catalog/product/view/id/1260852026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08047-1-gba2-primary-antibodies-wb-testing-1.jpgAnti-GBA2 Antibody Picoband® Western blot analysis of GBA2 using anti-GBA2 antibody (A08047-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GBA2 antigen affinity purified polyclonal antibody (Catalog # A08047-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GBA2 at approximately 105 kDa. The expected band size for GBA2 is at 105 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08047-1-gba2-primary-antibodies-fcm-testing-2.pngAnti-GBA2 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-GBA2 antibody (A08047-1). Overlay histogram showing A549 cells stained with A08047-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GBA2 Antibody (A08047-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260862026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-wb-testing-1.jpgAnti-GCLC Antibody Picoband® Western blot analysis of GCLC using anti-GCLC antibody (A01722). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GCLC antigen affinity purified polyclonal antibody (Catalog # A01722) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GCLC at approximately 73 kDa. The expected band size for GCLC is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-ihc-testing-2.jpgAnti-GCLC Antibody Picoband® IHC analysis of GCLC using anti-GCLC antibody (A01722). GCLC was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GCLC Antibody (A01722) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-ihc-testing-3.jpgAnti-GCLC Antibody Picoband® IHC analysis of GCLC using anti-GCLC antibody (A01722). GCLC was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GCLC Antibody (A01722) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-ihc-testing-4.jpgAnti-GCLC Antibody Picoband® IHC analysis of GCLC using anti-GCLC antibody (A01722). GCLC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GCLC Antibody (A01722) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-ihc-testing-5.jpgAnti-GCLC Antibody Picoband® IHC analysis of GCLC using anti-GCLC antibody (A01722). GCLC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GCLC Antibody (A01722) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-fcm-testing-6.pngAnti-GCLC Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-GCLC antibody (A01722). Overlay histogram showing A549 cells stained with A01722 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GCLC Antibody (A01722, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-fcm-testing-7.pngAnti-GCLC Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-GCLC antibody (A01722). Overlay histogram showing MCF-7 cells stained with A01722 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GCLC Antibody (A01722, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01722-gclc-primary-antibodies-if-testing-8.jpgAnti-GCLC Antibody Picoband® IF analysis of GCLC using anti-GCLC antibody (A01722). GCLC was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-GCLC Antibody (A01722) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1260882026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12538-1-nol11-primary-antibodies-wb-testing-1.jpgAnti-NOL11 Antibody Picoband® Western blot analysis of NOL11 using anti-NOL11 antibody (A12538-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOL11 antigen affinity purified polyclonal antibody (Catalog # A12538-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOL11 at approximately 90 kDa. The expected band size for NOL11 is at 81 kDa. https://www.bosterbio.com/catalog/product/view/id/1260892026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09446-1-nsun4-primary-antibodies-wb-testing-1.jpgAnti-NSUN4 Antibody Picoband® Western blot analysis of NSUN4 using anti-NSUN4 antibody (A09446-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSUN4 antigen affinity purified polyclonal antibody (Catalog # A09446-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSUN4 at approximately 40 kDa. The expected band size for NSUN4 is at 43 kDa. https://www.bosterbio.com/catalog/product/view/id/1260902026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08224-ndufa1-primary-antibodies-wb-testing-1.jpgAnti-NDUFA1 Antibody Picoband® Western blot analysis of NDUFA1 using anti-NDUFA1 antibody (A08224). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat liver tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFA1 antigen affinity purified polyclonal antibody (Catalog # A08224) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NDUFA1 at approximately 10 kDa. The expected band size for NDUFA1 is at 8 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08224-ndufa1-primary-antibodies-wb-testing-2.jpgAnti-NDUFA1 Antibody Picoband® Western blot analysis of NDUFA1 using anti-NDUFA1 antibody (A08224). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFA1 antigen affinity purified polyclonal antibody (A08224) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NDUFA1 at approximately 10 kDa. The expected band size for NDUFA1 is at 8 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08224-ndufa1-primary-antibodies-ihc-testing-3_1.jpgAnti-NDUFA1 Antibody Picoband® IHC analysis of NDUFA1 using anti-NDUFA1 antibody (A08224). NDUFA1 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA1 Antibody (A08224) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08224-ndufa1-primary-antibodies-ihc-testing-4.jpgAnti-NDUFA1 Antibody Picoband® IHC analysis of NDUFA1 using anti-NDUFA1 antibody (A08224). NDUFA1 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFA1 Antibody (A08224) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1260912026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08120-2-nip7-primary-antibodies-wb-testing-1.jpgAnti-NIP7 Antibody Picoband® Western blot analysis of NIP7 using anti-NIP7 antibody (A08120-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NIP7 antigen affinity purified polyclonal antibody (Catalog # A08120-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NIP7 at approximately 20 kDa. The expected band size for NIP7 is at 20 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08120-2-nip7-primary-antibodies-fcm-testing-2.pngAnti-NIP7 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NIP7 antibody (A08120-2). Overlay histogram showing 293T cells stained with A08120-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NIP7 Antibody (A08120-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260922026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00851-2-gh1-primary-antibodies-wb-testing-1.jpgAnti-GH1 Antibody Picoband® Western blot analysis of GH1 using anti-GH1 antibody (A00851-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates, Lane 7: mouse 3T3-L1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GH1 antigen affinity purified polyclonal antibody (Catalog # A00851-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GH1 at approximately 22 kDa. The expected band size for GH1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00851-2-gh1-primary-antibodies-fcm-testing-2.pngAnti-GH1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-GH1 antibody (A00851-2). Overlay histogram showing HEL cells stained with A00851-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GH1 Antibody (A00851-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260932026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14236-gigyf1-primary-antibodies-wb-testing-1.jpgAnti-GIGYF1 Antibody Picoband® Western blot analysis of GIGYF1 using anti-GIGYF1 antibody (A14236). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GIGYF1 antigen affinity purified polyclonal antibody (Catalog # A14236) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GIGYF1 at approximately 150 kDa. The expected band size for GIGYF1 is at 115 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14236-gigyf1-primary-antibodies-fcm-testing-2.pngAnti-GIGYF1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-GIGYF1 antibody (A14236). Overlay histogram showing SH-SY5Y cells stained with A14236 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GIGYF1 Antibody (A14236, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/catalog/product/view/id/1260942026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11144-1-gimap1-primary-antibodies-wb-testing-1.jpgAnti-GIMAP1 Antibody Picoband® Western blot analysis of GIMAP1 using anti-GIMAP1 antibody (A11144-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GIMAP1 antigen affinity purified polyclonal antibody (Catalog # A11144-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GIMAP1 at approximately 36 kDa. The expected band size for GIMAP1 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11144-1-gimap1-primary-antibodies-fcm-testing-2.pngAnti-GIMAP1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-GIMAP1 antibody (A11144-1). Overlay histogram showing JK cells stained with A11144-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GIMAP1 Antibody (A11144-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11144-1-gimap1-primary-antibodies-fcm-testing-3.pngAnti-GIMAP1 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-GIMAP1 antibody (A11144-1). Overlay histogram showing JK cells stained with A11144-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GIMAP1 Antibody (A11144-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. U2OS sample (Black line) was used as a negative control. https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-integrin-a6-dz41484-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-integrin-bc-dz41486-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-integrin-bg-dz41518-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-integrin-b1a-dz41543-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-jabba-isoform-e-dz41544-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-twist-dz41509-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-vdac-dz41510-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-ip3-receptor-dz41511-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-drp1-dz41512-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-opa1-dz41513-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-influenza-a-virus-cali-dz41526-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-bobtail-squid-adar2-dz41545-boster.html2026-03-10T04:37:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261262026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00611-3-sirt6-primary-antibodies-wb-testing-1.jpgAnti-SIRT6 Antibody Picoband® Western blot analysis of SIRT6 using anti-SIRT6 antibody (A00611-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIRT6 antigen affinity purified polyclonal antibody (Catalog # A00611-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SIRT6 at approximately 45 kDa. The expected band size for SIRT6 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00611-3-sirt6-primary-antibodies-if-testing-2.jpgAnti-SIRT6 Antibody Picoband® IF analysis of SIRT6 using anti-SIRT6 antibody (A00611-3) and anti-Beta Tubulin antibody (M01857-3). SIRT6 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SIRT6 Antibody (A00611-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) and DyLight®488 Conjugated Goat Anti-Mouse IgG (BA1126) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00611-3-sirt6-primary-antibodies-fcm-testing-3.pngAnti-SIRT6 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-SIRT6 antibody (A00611-3). Overlay histogram showing Hela cells stained with A00611-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SIRT6 Antibody (A00611-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample (Red line) was also used as a control. https://www.bosterbio.com/products/all-secondary-antibodies/dylight-reg-647-conjugated-goat-anti-rabbit-igg-ba1150-boster.html2026-03-10T04:37:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/a/ba1150-wb-1_1.jpgGoat Anti-Rabbit IgG (H+L) Secondary Antibody, Fluoro647 ConjugatedFigure 1. Western blot analysis of APEX1 using anti-APEX1 antibody (PB9128). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: human A549 whole cell lysates, Lane 6: human MCF-7 whole cell lysates, Lane 7: human RT4 whole cell lysates, Lane 8: human U87 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APEX1 antigen affinity purified polyclonal antibody (Catalog # PB9128) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-Fluoro647 Conjugated secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. A specific band was detected for APEX1 at approximately 36 kDa. The expected band size for APEX1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/a/ba1150-if-2_1.jpgGoat Anti-Rabbit IgG (H+L) Secondary Antibody, Fluoro647 Conjugated IF analysis of COX5B using anti-COX5B antibody (A06090-2). COX5B was detected in a paraffin-embedded section of human intestinal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-COX5B Antibody (A06090-2) overnight at 4°C. Fluoro647 Conjugated Goat Anti-Rabbit IgG (BA1150) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/all-secondary-antibodies/dylight-reg-647-conjugated-goat-anti-mouse-igg-ba1151-boster.html2026-03-10T04:37:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/a/ba1151-wb-1_1.jpgGoat Anti-Mouse IgG (H+L) Secondary Antibody, Fluoro647 ConjugatedWestern blot analysis of KPNB1 using anti-KPNB1 antibody (M01851-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human CACO-2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat NRK whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with mouse anti-KPNB1 antigen affinity purified monoclonal antibody (M01851-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-mouse IgG-Fluoro 647 secondary antibody (Catalog # BA1151) at a dilution of 1:2000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for KPNB1 at approximately 97 kDa. The expected band size for KPNB1 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/a/ba1151-if-2_1.jpgGoat Anti-Mouse IgG (H+L) Secondary Antibody, Fluoro647 Conjugated IF analysis of NEFH using anti-NEFH antibody (MA1071). NEFH was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL mouse anti-NEFH Antibody (MA1071) overnight at 4°C. Fluoro647 Conjugated Goat Anti-Mouse IgG (BA1151) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/a/ba1151-if-3_1.jpgGoat Anti-Mouse IgG (H+L) Secondary Antibody, Fluoro647 Conjugated IF analysis of NEFH using anti-NEFH antibody (MA1071). NEFH was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL mouse anti-NEFH Antibody (MA1071) overnight at 4°C. Fluoro647 Conjugated Goat Anti-Mouse IgG (BA1151) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1261292026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00629-4-crf-crh-primary-antibodies-wb-testing-1.jpgAnti-CRF/CRH Antibody Picoband® Western blot analysis of CRF/CRH using anti-CRF/CRH antibody (A00629-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U-87MG whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Neuro-2a whole cell lysates, After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CRF/CRH antigen affinity purified polyclonal antibody (A00629-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CRF/CRH at approximately 25 kDa. The expected band size for CRF/CRH is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00629-4-crf-crh-primary-antibodies-fcm-testing-2.jpgAnti-CRF/CRH Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-CRF/CRH antibody (A00629-4). Overlay histogram showing U251 cells stained with A00629-4 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CRF/CRH Antibody (A00629-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261302026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261312026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02406-2-pex5-primary-antibodies-wb-testing-1.jpgAnti-PEX5 Antibody Picoband®Western blot analysis of PEX5 using anti-PEX5 antibody (A02406-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat kidney tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PEX5 antigen affinity purified polyclonal antibody (A02406-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PEX5 at approximately 80 kDa. The expected band size for PEX5 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02406-2-pex5-primary-antibodies-ihc-testing-1.jpgAnti-PEX5 Antibody Picoband®IHC analysis of PEX5 using anti-PEX5 antibody (A02406-2). PEX5 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PEX5 Antibody (A02406-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02406-2-pex5-primary-antibodies-fcm-testing-1.jpgAnti-PEX5 Antibody Picoband®Flow Cytometry analysis of RT4 cells using anti-PEX5 antibody (A02406-2). Overlay histogram showing RT4 cells stained with A02406-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PEX5 Antibody (A02406-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261322026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06602-1-stx16-primary-antibodies-wb-testing-1.jpgAnti-Syntaxin 16/STX16 Antibody Picoband®Western blot analysis of Syntaxin 16/STX16 using anti-Syntaxin 16/STX16 antibody (A06602-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat spleen tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Syntaxin 16/STX16 antigen affinity purified polyclonal antibody (A06602-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Syntaxin 16/STX16 at approximately 37 kDa. The expected band size for Syntaxin 16/STX16 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06602-1-stx16-primary-antibodies-fcm-testing-1.jpgAnti-Syntaxin 16/STX16 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-Syntaxin 16/STX16 antibody (A06602-1). Overlay histogram showing 293T cells stained with A06602-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Syntaxin 16/STX16 Antibody (A06602-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261332026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05499-2-ftcd-primary-antibodies-wb-testing-1.jpgAnti-FTCD Antibody Picoband®Western blot analysis of FTCD using anti-FTCD antibody (A05499-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FTCD antigen affinity purified polyclonal antibody (A05499-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FTCD at approximately 59 kDa. The expected band size for FTCD is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05499-2-ftcd-primary-antibodies-ihc-testing-1.jpgAnti-FTCD Antibody Picoband®IHC analysis of FTCD using anti-FTCD antibody (A05499-2). FTCD was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FTCD Antibody (A05499-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05499-2-ftcd-primary-antibodies-ihc-testing-2.jpgAnti-FTCD Antibody Picoband®IHC analysis of FTCD using anti-FTCD antibody (A05499-2). FTCD was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FTCD Antibody (A05499-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05499-2-ftcd-primary-antibodies-if-testing-1.jpgAnti-FTCD Antibody Picoband®IF analysis of FTCD using anti-FTCD antibody (A05499-2). FTCD was detected in an immunocytochemical section of HepG2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-FTCD Antibody (A05499-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1261352026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261372026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261382026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261392026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261402026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261412026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14356-2-trim46-primary-antibodies-wb-testing-1_1.jpgAnti-TRIM46 Antibody Picoband®Western blot analysis of TRIM46 using anti-TRIM46 antibody (A14356-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat hippocampus tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse hippocampus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIM46 antigen affinity purified polyclonal antibody (A14356-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIM46 at approximately 83 kDa. The expected band size for TRIM46 is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14356-2-trim46-primary-antibodies-ihc-testing-1.jpgAnti-TRIM46 Antibody Picoband®IHC analysis of TRIM46 using anti-TRIM46 antibody (A14356-2). TRIM46 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM46 Antibody (A14356-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14356-2-trim46-primary-antibodies-ihc-testing-2.jpgAnti-TRIM46 Antibody Picoband®IHC analysis of TRIM46 using anti-TRIM46 antibody (A14356-2). TRIM46 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM46 Antibody (A14356-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14356-2-trim46-primary-antibodies-ihc-testing-3.jpgAnti-TRIM46 Antibody Picoband®IHC analysis of TRIM46 using anti-TRIM46 antibody (A14356-2). TRIM46 was detected in a paraffin-embedded section of human cerebral cortex tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM46 Antibody (A14356-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261422026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261432026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261442026-03-13T05:05:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01420-1-prkaa2-primary-antibodies-wb-testing-1.jpgAnti-AMPK Alpha 2/PRKAA2 antibodyWestern blot analysis of PRKAA2 using anti-PRKAA2 antibody (A01420-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human SK-OV-3 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat ovary tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRKAA2 antigen affinity purified polyclonal antibody (A01420-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PRKAA2 at approximately 62 kDa. The expected band size for PRKAA2 is at 62 kDa. https://www.bosterbio.com/catalog/product/view/id/1261452026-03-13T05:05:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00697-myh7-specific-primary-antibodies-wb-testing-1.jpgAnti-MYH7-Specific antibodyWestern blot analysis of MYH7-Specific using anti-MYH7-Specific antibody (A00697). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: rat skeletal muscle tissue lysates, Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYH7-Specific antigen affinity purified polyclonal antibody (A00697) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MYH7-Specific at approximately 220 kDa. The expected band size for MYH7-Specific is at 223 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00697-myh7-specific-primary-antibodies-ihc-testing-1.jpgAnti-MYH7-Specific antibodyIHC analysis of MYH7-Specific using anti-MYH7-Specific antibody (A00697). MYH7-Specific was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MYH7-Specific Antibody (A00697) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261462026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261472026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261482026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261492026-03-16T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05441-1-fdx1-primary-antibodies-wb-testing-1.jpgAnti-FDX1 antibody Western blot analysis of FDX1 using anti-FDX1 antibody (A05441-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat ovary tissue lysates, Lane 6: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FDX1 antigen affinity purified polyclonal antibody (A05441-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FDX1 at approximately 14 kDa. The expected band size for FDX1 is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05441-1-fdx1-primary-antibodies-ihc-testing-2.jpgAnti-FDX1 antibody IHC analysis of FDX1 using anti-FDX1 antibody (A05441-1). FDX1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FDX1 Antibody (A05441-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05441-1-fdx1-primary-antibodies-ihc-testing-3.jpgAnti-FDX1 antibody IHC analysis of FDX1 using anti-FDX1 antibody (A05441-1). FDX1 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FDX1 Antibody (A05441-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261502026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261512026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32407-2-dfna5-gsdme-primary-antibodies-wb-testing-1.jpgAnti-GSDME Antibody Picoband® Western blot analysis of DFNA5/GSDME using anti-DFNA5/GSDME antibody (A32407-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DFNA5/GSDME antigen affinity purified polyclonal antibody (A32407-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DFNA5/GSDME at approximately 55 kDa. The expected band size for DFNA5/GSDME is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32407-2-gsdme-primary-antibodies-ihc-testing-1.jpgAnti-GSDME Antibody Picoband®IHC analysis of DFNA5/GSDME using anti-DFNA5/GSDME antibody (A32407-2). DFNA5/GSDME was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DFNA5/GSDME Antibody (A32407-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32407-2-gsdme-primary-antibodies-wb-testing-1.jpgAnti-GSDME Antibody Picoband®Western blot analysis of GSDME using anti-GSDME antibody (A32407-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSDME antigen affinity purified polyclonal antibody (A32407-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GSDME at approximately 55 kDa. The expected band size for GSDME is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32407-2-gsdme-primary-antibodies-if-testing-1.jpgAnti-GSDME Antibody Picoband®IF analysis of GSDME using anti-GSDME antibody (A32407-2). GSDME was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GSDME Antibody (A32407-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32407-2-gsdme-primary-antibodies-ip-testing-1.jpgAnti-GSDME Antibody Picoband®Immunoprecipitating GSDME in Hela whole cell lysate. Western blot analysis of GSDME using anti-GSDME antibody (A32407-2). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-GSDME antibody in Hela whole cell lysate, Lane 3: anti-GSDME antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GSDME antigen affinity purified polyclonal antibody (A32407-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GSDME at approximately 55 kDa. The expected band size for GSDME is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32407-2-gsdme-primary-antibodies-fcm-testing-1.jpgAnti-GSDME Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-GSDME antibody (A32407-2). Overlay histogram showing SH-SY5Y cells stained with A32407-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GSDME Antibody (A32407-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261522026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00289-1-drd2-primary-antibodies-wb-testing-1.jpgAnti-DRD2 antibodyWestern blot analysis of DRD2 using anti-DRD2 antibody (A00289-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DRD2 antigen affinity purified polyclonal antibody (A00289-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DRD2 at approximately 50-60 kDa. The expected band size for DRD2 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00289-1-drd2-primary-antibodies-ihc-testing-1.jpgAnti-DRD2 antibodyIHC analysis of DRD2 using anti-DRD2 antibody (A00289-1). DRD2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-DRD2 Antibody (A00289-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00289-1-drd2-primary-antibodies-ihc-testing-2.jpgAnti-DRD2 antibodyIHC analysis of DRD2 using anti-DRD2 antibody (A00289-1). DRD2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-DRD2 Antibody (A00289-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00289-1-drd2-primary-antibodies-ihc-testing-3.jpgAnti-DRD2 antibodyIHC analysis of DRD2 using anti-DRD2 antibody (A00289-1). DRD2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-DRD2 Antibody (A00289-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00289-1-drd2-primary-antibodies-ihc-testing-4.jpgAnti-DRD2 antibodyIHC analysis of DRD2 using anti-DRD2 antibody (A00289-1). DRD2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-DRD2 Antibody (A00289-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00289-1-drd2-primary-antibodies-ihc-testing-5.jpgAnti-DRD2 antibodyIHC analysis of DRD2 using anti-DRD2 antibody (A00289-1). DRD2 was detected in a paraffin-embedded section of pig brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-DRD2 Antibody (A00289-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261532026-03-13T05:05:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00199-2-wt1-primary-antibodies-ihc-testing-1.jpgAnti-WT1 antibodyIHC analysis of WT1 using anti-WT1 antibody (A00199-2). WT1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-WT1 Antibody (A00199-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261542026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261552026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05579-2-psph-primary-antibodies-wb-testing-1.jpgAnti-PSPH Antibody Picoband®Western blot analysis of Phosphoserine/PSPH using anti-Phosphoserine/PSPH antibody (A05579-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates, Lane 2: human HL-60 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human U-87MG whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse HEPA1-6 tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Phosphoserine/PSPH antigen affinity purified polyclonal antibody (A05579-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Phosphoserine/PSPH at approximately 25 kDa. The expected band size for Phosphoserine/PSPH is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05579-2-psph-primary-antibodies-wb-testing-1_1.jpgAnti-PSPH Antibody Picoband®Western blot analysis of PSPH using anti-PSPH antibody (A05579-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: rat RH35 whole cell lysates, Lane 4: mouse liver tissue lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSPH antigen affinity purified polyclonal antibody (A05579-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PSPH at approximately 26 kDa. The expected band size for PSPH is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05579-2-psph-primary-antibodies-ihc-testing-1.jpgAnti-PSPH Antibody Picoband®IHC analysis of PSPH using anti-PSPH antibody (A05579-2). PSPH was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PSPH Antibody (A05579-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05579-2-psph-primary-antibodies-if-testing-1.jpgAnti-PSPH Antibody Picoband®IF analysis of PSPH using anti-PSPH antibody (A05579-2). PSPH was detected in an immunocytochemical section of SIHA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PSPH Antibody (A05579-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1261562026-03-13T05:05:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01684-3-oas1-3-primary-antibodies-wb-testing-1.jpgAnti-OAS1/3 antibody Western blot analysis of OAS1/3 using anti-OAS1/3 antibody (A01684-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OAS1/3 antigen affinity purified polyclonal antibody (A01684-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for OAS1/3 at approximately 105 kDa. The expected band size for OAS1/3 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01684-3-oas1-3-primary-antibodies-ihc-testing-1.jpgAnti-OAS1/3 antibodyIHC analysis of OAS1/3 using anti-OAS1/3 antibody (A01684-3). OAS1/3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OAS1/3 Antibody (A01684-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01684-3-oas1-3-primary-antibodies-ihc-testing-2.jpgAnti-OAS1/3 antibodyIHC analysis of OAS1/3 using anti-OAS1/3 antibody (A01684-3). OAS1/3 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OAS1/3 Antibody (A01684-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261572026-03-13T05:05:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01877-1-pabp-primary-antibodies-wb-testing-1.jpgAnti-PABP/PABPC1 antibodyWestern blot analysis of PABP using anti-PABP antibody (A01877-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PABP antigen affinity purified polyclonal antibody (A01877-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PABP at approximately 71 kDa. The expected band size for PABP is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01877-1-pabp-primary-antibodies-ihc-testing-1.jpgAnti-PABP/PABPC1 antibodyIHC analysis of PABP using anti-PABP antibody (A01877-1). PABP was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-PABP Antibody (A01877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01877-1-pabp-primary-antibodies-ihc-testing-2.jpgAnti-PABP/PABPC1 antibodyIHC analysis of PABP using anti-PABP antibody (A01877-1). PABP was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-PABP Antibody (A01877-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261582026-03-16T05:08:28+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261592026-03-16T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05156-2-fech-primary-antibodies-wb-testing-1.jpgAnti-FECH antibody Western blot analysis of FECH using anti-FECH antibody (A05156-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FECH antigen affinity purified polyclonal antibody (A05156-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FECH at approximately 48 kDa. The expected band size for FECH is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05156-2-fech-primary-antibodies-ihc-testing-2.jpgAnti-FECH antibody IHC analysis of FECH using anti-FECH antibody (A05156-2). FECH was detected in a paraffin-embedded section of human benign Prostate Hyperplasia tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FECH Antibody (A05156-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05156-2-fech-primary-antibodies-ihc-testing-3.jpgAnti-FECH antibody IHC analysis of FECH using anti-FECH antibody (A05156-2). FECH was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-FECH Antibody (A05156-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261602026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-wb-testing-1.jpgAnti-BAP31/BCAP31 Antibody Picoband® Western blot analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human placenta tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BAP31/BCAP31 antigen affinity purified polyclonal antibody (Catalog # A03767-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BAP31/BCAP31 at approximately 28 kDa. The expected band size for BAP31/BCAP31 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-ihc-testing-2.jpgAnti-BAP31/BCAP31 Antibody Picoband® IHC analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-ihc-testing-3.jpgAnti-BAP31/BCAP31 Antibody Picoband® IHC analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-ihc-testing-4.jpgAnti-BAP31/BCAP31 Antibody Picoband® IHC analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-ihc-testing-5.jpgAnti-BAP31/BCAP31 Antibody Picoband® IHC analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-ihc-testing-6.jpgAnti-BAP31/BCAP31 Antibody Picoband® IHC analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-ihc-testing-7.jpgAnti-BAP31/BCAP31 Antibody Picoband® IHC analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-if-testing-8.jpgAnti-BAP31/BCAP31 Antibody Picoband® IF analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-if-testing-1.jpgAnti-BAP31/BCAP31 Antibody Picoband®IF analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-if-testing-2.jpgAnti-BAP31/BCAP31 Antibody Picoband®IF analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4). BAP31/BCAP31 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-BAP31/BCAP31 Antibody (A03767-4) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-ip-testing-1.jpgAnti-BAP31/BCAP31 Antibody Picoband®Immunoprecipitating (IP) BAP31/BCAP31 in A431 whole cell lysate. Western blot analysis of BAP31/BCAP31 using anti-BAP31/BCAP31 antibody (A03767-4); Lane 1: A431 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-BAP31/BCAP31 antibody in A431 whole cell lysate; Lane 3: anti-BAP31/BCAP31 antibody (2μg) + A431 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BAP31/BCAP31 antigen affinity purified polyclonal antibody (A03767-4) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for BAP31/BCAP31 at approximately 28 kDa. The expected band size for BAP31/BCAP31 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03767-4-bcap31-primary-antibodies-fcm-testing-9.jpgAnti-BAP31/BCAP31 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-BAP31/BCAP31 antibody (A03767-4). Overlay histogram showing A431 cells stained with A03767-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BAP31/BCAP31 Antibody (A03767-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261612026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00845-2-pax7-primary-antibodies-wb-testing-1.jpgAnti-PAX7 Antibody Picoband®Western blot analysis of PAX7 using anti-PAX7 antibody (A00845-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PAX7 antigen affinity purified polyclonal antibody (A00845-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PAX7 at approximately 55 kDa. The expected band size for PAX7 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00845-2-pax7-primary-antibodies-fcm-testing-1.jpgAnti-PAX7 Antibody Picoband®Flow Cytometry analysis of CACO-2 cells using anti-PAX7 antibody (A00845-2). Overlay histogram showing CACO-2 cells stained with A00845-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PAX7 Antibody (A00845-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261622026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03760-rtn3-primary-antibodies-ihc-testing-1.jpgAnti-RTN3 antibodyIHC analysis of RTN3 using anti-RTN3 antibody (A03760). RTN3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-RTN3 Antibody (A03760) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03760-rtn3-primary-antibodies-ihc-testing-2.jpgAnti-RTN3 antibodyIHC analysis of RTN3 using anti-RTN3 antibody (A03760). RTN3 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-RTN3 Antibody (A03760) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261632026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261642026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261652026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03640-2-bbs4-primary-antibodies-wb-testing-1.jpgAnti-BBS4 Antibody Picoband®Western blot analysis of BBS4 using anti-BBS4 antibody (A03640-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BBS4 antigen affinity purified polyclonal antibody (A03640-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for BBS4 at approximately 60 kDa. The expected band size for BBS4 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03640-2-bbs4-primary-antibodies-ip-testing-1.jpgAnti-BBS4 Antibody Picoband®Immunoprecipitating BBS4 in 293T whole cell lysate. Western blot analysis of BBS4 using anti-BBS4 antibody (A03640-2). Lane 1: 293T whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-BBS4 antibody in 293T whole cell lysate, Lane 3: anti-BBS4 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-BBS4 antigen affinity purified polyclonal antibody (A03640-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for BBS4 at approximately 60 kDa. The expected band size for BBS4 is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03640-2-bbs4-primary-antibodies-fcm-testing-1.jpgAnti-BBS4 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-BBS4 antibody (A03640-2). Overlay histogram showing 293T cells stained with A03640-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BBS4 Antibody (A03640-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261662026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04012-2-krt6a-primary-antibodies-wb-testing-1.jpgAnti-Cytokeratin 6A/KRT6A antibodyWestern blot analysis of Cytokeratin 6A/KRT6A using anti-Cytokeratin 6A/KRT6A antibody (A04012-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human A375 whole cell lysates, Lane 3: rat kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cytokeratin 6A/KRT6A antigen affinity purified polyclonal antibody (A04012-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Cytokeratin 6A/KRT6A at approximately 60 kDa. The expected band size for Cytokeratin 6A/KRT6A is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04012-2-krt6a-primary-antibodies-ihc-testing-1.jpgAnti-Cytokeratin 6A/KRT6A antibodyIHC analysis of Cytokeratin 6A/KRT6A using anti-Cytokeratin 6A/KRT6A antibody (A04012-2). Cytokeratin 6A/KRT6A was detected in a paraffin-embedded section of human skin cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Cytokeratin 6A/KRT6A Antibody (A04012-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04012-2-krt6a-primary-antibodies-ihc-testing-2.jpgAnti-Cytokeratin 6A/KRT6A antibodyIHC analysis of Cytokeratin 6A/KRT6A using anti-Cytokeratin 6A/KRT6A antibody (A04012-2). Cytokeratin 6A/KRT6A was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Cytokeratin 6A/KRT6A Antibody (A04012-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04012-2-krt6a-primary-antibodies-ihc-testing-3.jpgAnti-Cytokeratin 6A/KRT6A antibodyIHC analysis of Cytokeratin 6A/KRT6A using anti-Cytokeratin 6A/KRT6A antibody (A04012-2). Cytokeratin 6A/KRT6A was detected in a paraffin-embedded section of rat skin tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-Cytokeratin 6A/KRT6A Antibody (A04012-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261672026-03-16T05:08:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08869-1-asrgl1-primary-antibodies-wb-testing-1.jpgAnti-ASRGL1 antibody Western blot analysis of ASRGL1 using anti-ASRGL1 antibody (A08869-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ASRGL1 antigen affinity purified polyclonal antibody (A08869-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ASRGL1 at approximately 36-38 kDa. The expected band size for ASRGL1 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08869-1-asrgl1-primary-antibodies-ihc-testing-1.jpgAnti-ASRGL1 antibodyIHC analysis of ASRGL1 using anti-ASRGL1 antibody (A08869-1). ASRGL1 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASRGL1 Antibody (A08869-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261682026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261692026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00842-1-fxn-primary-antibodies-wb-testing-1.jpgAnti-FXN Antibody Picoband®Western blot analysis of FXN using anti-FXN antibody (A00842-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FXN antigen affinity purified polyclonal antibody (A00842-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FXN at approximately 14 kDa. The expected band size for FXN is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00842-1-fxn-primary-antibodies-ihc-testing-1.jpgAnti-FXN Antibody Picoband®IHC analysis of FXN using anti-FXN antibody (A00842-1). FXN was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FXN Antibody (A00842-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00842-1-fxn-primary-antibodies-ihc-testing-2.jpgAnti-FXN Antibody Picoband®IHC analysis of FXN using anti-FXN antibody (A00842-1). FXN was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FXN Antibody (A00842-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00842-1-fxn-primary-antibodies-ihc-testing-3.jpgAnti-FXN Antibody Picoband®IHC analysis of FXN using anti-FXN antibody (A00842-1). FXN was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FXN Antibody (A00842-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00842-1-fxn-primary-antibodies-fcm-testing-1.jpgAnti-FXN Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-FXN antibody (A00842-1). Overlay histogram showing HepG2 cells stained with A00842-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FXN Antibody (A00842-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261702026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-3-gsta1-primary-antibodies-ihc-testing-1.jpgAnti-GSTA1 antibodyIHC analysis of GSTA1 using anti-GSTA1 antibody (A01462-3). GSTA1 was detected in a paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GSTA1 Antibody (A01462-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-3-gsta1-primary-antibodies-ihc-testing-2.jpgAnti-GSTA1 antibodyIHC analysis of GSTA1 using anti-GSTA1 antibody (A01462-3). GSTA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GSTA1 Antibody (A01462-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-3-gsta1-primary-antibodies-ihc-testing-3.jpgAnti-GSTA1 antibodyIHC analysis of GSTA1 using anti-GSTA1 antibody (A01462-3). GSTA1 was detected in a paraffin-embedded section of mouse liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-GSTA1 Antibody (A01462-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01462-3-gsta1-primary-antibodies-wb-testing-1.jpgAnti-GSTA1 antibodyWestern blot analysis of GSTA1 using anti-GSTA1 antibody (A01462-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HCCT tissue lysates, Lane 2: human HCCP tissue lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse kidney tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GSTA1 antigen affinity purified polyclonal antibody (A01462-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GSTA1 at approximately 26 kDa. The expected band size for GSTA1 is at 26 kDa. https://www.bosterbio.com/catalog/product/view/id/1261712026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16029-1-mas1l-primary-antibodies-ihc-testing-1.jpgAnti-MAS1L antibodyIHC analysis of MAS1L using anti-MAS1L antibody (A16029-1). MAS1L was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MAS1L Antibody (A16029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16029-1-mas1l-primary-antibodies-ihc-testing-2.jpgAnti-MAS1L antibodyIHC analysis of MAS1L using anti-MAS1L antibody (A16029-1). MAS1L was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MAS1L Antibody (A16029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16029-1-mas1l-primary-antibodies-ihc-testing-3.jpgAnti-MAS1L antibodyIHC analysis of MAS1L using anti-MAS1L antibody (A16029-1). MAS1L was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MAS1L Antibody (A16029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16029-1-mas1l-primary-antibodies-ihc-testing-4.jpgAnti-MAS1L antibodyIHC analysis of MAS1L using anti-MAS1L antibody (A16029-1). MAS1L was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-MAS1L Antibody (A16029-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261722026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261732026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261742026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261752026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261762026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261772026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261782026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261792026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261802026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261812026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261822026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261832026-03-16T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05241-1-1-sh3pxd2a-primary-antibodies-wb-testing-1.jpgAnti-SH3PXD2A antibodyWestern blot analysis of SH3PXD2A using anti-SH3PXD2A antibody (A05241-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat PC-12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SH3PXD2A antigen affinity purified polyclonal antibody (A05241-1) at 1: 1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SH3PXD2A at approximately 150 kDa. The expected band size for SH3PXD2A is at 125 kDa. https://www.bosterbio.com/catalog/product/view/id/1261842026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261852026-03-16T05:08:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07184-3-usp36-primary-antibodies-wb-testing-1.jpgAnti-USP36 antibodyWestern blot analysis of USP36 using anti-USP36 antibody (A07184-3). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-USP36 antigen affinity purified polyclonal antibody (A07184-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for USP36 at approximately 150 kDa. The expected band size for USP36 is at 123 kDa. https://www.bosterbio.com/catalog/product/view/id/1261862026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261872026-03-13T05:05:06+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261882026-03-13T05:05:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03954-3-cep55-primary-antibodies-wb-testing-1.jpgAnti-CEP55 antibody Western blot analysis of CEP55 using anti-CEP55 antibody (A03954-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CEP55 antigen affinity purified polyclonal antibody (A03954-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CEP55 at approximately 54 kDa. The expected band size for CEP55 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03954-3-cep55-primary-antibodies-ihc-testing-2.jpgAnti-CEP55 antibody IHC analysis of CEP55 using anti-CEP55 antibody (A03954-3). CEP55 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CEP55 Antibody (A03954-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03954-3-cep55-primary-antibodies-ihc-testing-3.jpgAnti-CEP55 antibody IHC analysis of CEP55 using anti-CEP55 antibody (A03954-3). CEP55 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CEP55 Antibody (A03954-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03954-3-cep55-primary-antibodies-ihc-testing-4.jpgAnti-CEP55 antibody IHC analysis of CEP55 using anti-CEP55 antibody (A03954-3). CEP55 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-CEP55 Antibody (A03954-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1261892026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261902026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261912026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01760-1-map1b-primary-antibodies-wb-testing-1.jpgAnti-MAP1B Antibody Picoband® Western blot analysis of MAP1B using anti-MAP1B antibody (A01760-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAP1B antigen affinity purified polyclonal antibody (A01760-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MAP1B at approximately 310 kDa. The expected band size for MAP1B is at 271 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01760-1-map1b-primary-antibodies-ihc-testing-2.jpgAnti-MAP1B Antibody Picoband® IHC analysis of MAP1B using anti-MAP1B antibody (A01760-1). MAP1B was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP1B Antibody (A01760-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01760-1-map1b-primary-antibodies-ihc-testing-3.jpgAnti-MAP1B Antibody Picoband® IHC analysis of MAP1B using anti-MAP1B antibody (A01760-1). MAP1B was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MAP1B Antibody (A01760-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01760-1-map1b-primary-antibodies-if-testing-4.jpgAnti-MAP1B Antibody Picoband®IF analysis of MAP1B using anti-MAP1B antibody (A01760-1). MAP1B was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 4 μg/mL rabbit anti-MAP1B Antibody (A01760-1) overnight at 4°C. HRP conjugated goat anti-rabbit IgG (BA1054) was used as secondary antibody and incubated for 30 minutes at 37°C. Tyramide signal amplification was performed using TSA 620 reagent at 1:200 dilution at room temperature for 10 minutes. Visualize using a fluorescence microscope and filter sets appropriate for the label used. Fluorescence signals were visualized using a fluorescence microscope with filter sets appropriate for TSA 620 and DAPI.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01760-1-map1b-primary-antibodies-if-testing-5.jpgAnti-MAP1B Antibody Picoband®IF analysis of MAP1B using anti-MAP1B antibody (A01760-1). MAP1B was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 4 μg/mL rabbit anti-MAP1B Antibody (A01760-1) overnight at 4°C. HRP conjugated goat anti-rabbit IgG (BA1054) was used as secondary antibody and incubated for 30 minutes at 37°C. Tyramide signal amplification was performed using TSA 620 reagent at 1:200 dilution at room temperature for 10 minutes. Visualize using a fluorescence microscope and filter sets appropriate for the label used. Fluorescence signals were visualized using a fluorescence microscope with filter sets appropriate for TSA 620 and DAPI.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01760-1-map1b-primary-antibodies-fcm-testing-6.jpgAnti-MAP1B Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-MAP1B antibody (A01760-1). Overlay histogram showing A549 cells stained with A01760-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAP1B Antibody (A01760-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1261922026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04413-2-msra-primary-antibodies-wb-testing-1.jpgAnti-MSRA Antibody Picoband®Western blot analysis of MSRA using anti-MSRA antibody (A04413-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human SIHA whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MSRA antigen affinity purified polyclonal antibody (A04413-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MSRA at approximately 24 kDa. The expected band size for MSRA is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04413-2-msra-primary-antibodies-if-testing-1.jpgAnti-MSRA Antibody Picoband®IF analysis of MSRA using anti-MSRA antibody (A04413-2) and anti-Beta Tubulin antibody (M01857-3). MSRA was detected in an immunocytochemical section of SIHA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MSRA Antibody (A04413-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1261932026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261942026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261952026-03-16T05:08:29+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261962026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261972026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261982026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1261992026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262012026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01935-1-chmp2b-primary-antibodies-wb-testing-1.jpgAnti-CHMP2B antibody Picoband® Western blot analysis of CHMP2B using anti-CHMP2B antibody (A01935-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHMP2B antigen affinity purified polyclonal antibody (A01935-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHMP2B at approximately 28 kDa. The expected band size for CHMP2B is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01935-1-chmp2b-primary-antibodies-ihc-testing-1.jpgAnti-CHMP2B antibody Picoband® IHC analysis of CHMP2B using anti-CHMP2B antibody (A01935-1). CHMP2B was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHMP2B Antibody (A01935-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01935-1-chmp2b-primary-antibodies-ihc-testing-2.jpgAnti-CHMP2B antibody Picoband® IHC analysis of CHMP2B using anti-CHMP2B antibody (A01935-1). CHMP2B was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHMP2B Antibody (A01935-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01935-1-chmp2b-primary-antibodies-ihc-testing-3.jpgAnti-CHMP2B antibody Picoband® IHC analysis of CHMP2B using anti-CHMP2B antibody (A01935-1). CHMP2B was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHMP2B Antibody (A01935-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01935-1-chmp2b-primary-antibodies-ip-testing-1.jpgAnti-CHMP2B antibody Picoband® Immunoprecipitating (IP) CHMP2B in RT4 whole cell lysate. Western blot analysis of CHMP2B using anti-CHMP2B antibody (A01935-1); Lane 1: RT4 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-CHMP2B antibody in RT4 whole cell lysate; Lane 3: anti-CHMP2B antibody (2μg) + RT4 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-CHMP2B antigen affinity purified polyclonal antibody (A01935-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for CHMP2B at approximately 28 kDa. The expected band size for CHMP2B is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01935-1-chmp2b-primary-antibodies-fcm-testing-1.jpgAnti-CHMP2B antibody Picoband® Flow Cytometry analysis of A549 cells using anti-CHMP2B antibody (A01935-1). Overlay histogram showing A549 cells stained with A01935-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHMP2B Antibody (A01935-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262022026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262032026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11035-1-exoc5-primary-antibodies-wb-testing-1.jpgAnti-EXOC5 Antibody Picoband®Western blot analysis of EXOC5 using anti-EXOC5 antibody (A11035-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EXOC5 antigen affinity purified polyclonal antibody (A11035-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EXOC5 at approximately 77 kDa. The expected band size for EXOC5 is at 82 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11035-1-exoc5-primary-antibodies-ihc-testing-1.jpgAnti-EXOC5 Antibody Picoband®IHC analysis of EXOC5 using anti-EXOC5 antibody (A11035-1). EXOC5 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EXOC5 Antibody (A11035-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11035-1-exoc5-primary-antibodies-ihc-testing-2.jpgAnti-EXOC5 Antibody Picoband®IHC analysis of EXOC5 using anti-EXOC5 antibody (A11035-1). EXOC5 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EXOC5 Antibody (A11035-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262042026-03-13T05:05:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01431-1-lss-primary-antibodies-wb-testing-1.jpgAnti-LSS antibodyWestern blot analysis of LSS using anti-LSS antibody (A01431-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LSS antigen affinity purified polyclonal antibody (A01431-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LSS at approximately 75 kDa. The expected band size for LSS is at 83 kDa. https://www.bosterbio.com/catalog/product/view/id/1262052026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262062026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-wb-testing-1.jpgAnti-NSDHL Antibody Picoband®Western blot analysis of NSDHL using anti-NSDHL antibody (A04902-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSDHL antigen affinity purified polyclonal antibody (A04902-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NSDHL at approximately 38 kDa. The expected band size for NSDHL is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-ihc-testing-1.jpgAnti-NSDHL Antibody Picoband®IHC analysis of NSDHL using anti-NSDHL antibody (A04902-1). NSDHL was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSDHL Antibody (A04902-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-ihc-testing-2.jpgAnti-NSDHL Antibody Picoband®IHC analysis of NSDHL using anti-NSDHL antibody (A04902-1). NSDHL was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSDHL Antibody (A04902-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-ihc-testing-3.jpgAnti-NSDHL Antibody Picoband®IHC analysis of NSDHL using anti-NSDHL antibody (A04902-1). NSDHL was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSDHL Antibody (A04902-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-ihc-testing-4.jpgAnti-NSDHL Antibody Picoband®IHC analysis of NSDHL using anti-NSDHL antibody (A04902-1). NSDHL was detected in a paraffin-embedded section of rat liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSDHL Antibody (A04902-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-if-testing-1.jpgAnti-NSDHL Antibody Picoband®IF analysis of NSDHL using anti-NSDHL antibody (A04902-1). NSDHL was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NSDHL Antibody (A04902-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-if-testing-2.jpgAnti-NSDHL Antibody Picoband®IF analysis of NSDHL using anti-NSDHL antibody (A04902-1). NSDHL was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NSDHL Antibody (A04902-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-ip-testing-1.jpgAnti-NSDHL Antibody Picoband®Immunoprecipitating NSDHL in Hela whole cell lysate. Western blot analysis of NSDHL using anti-NSDHL antibody (A04902-1). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-NSDHL antibody in Hela whole cell lysate, Lane 3: anti-NSDHL antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NSDHL antigen affinity purified polyclonal antibody (A04902-1) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for NSDHL at approximately 38 kDa. The expected band size for NSDHL is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04902-1-nsdhl-primary-antibodies-fcm-testing-1.jpgAnti-NSDHL Antibody Picoband®Flow Cytometry analysis of A431 cells using anti-NSDHL antibody (A04902-1). Overlay histogram showing A431 cells stained with A04902-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSDHL Antibody (A04902-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262072026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-wb-testing-1.jpgAnti-PIP5K1A Antibody Picoband® Western blot analysis of PIP5K1A using anti-PIP5K1A antibody (A07416-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIP5K1A antigen affinity purified polyclonal antibody (A07416-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PIP5K1A at approximately 63 kDa. The expected band size for PIP5K1A is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-ihc-testing-2.jpgAnti-PIP5K1A Antibody Picoband® IHC analysis of PIP5K1A using anti-PIP5K1A antibody (A07416-3). PIP5K1A was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIP5K1A Antibody (A07416-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-ihc-testing-4.jpgAnti-PIP5K1A Antibody Picoband®IHC analysis of PIP5K1A using anti-PIP5K1A antibody (A07416-3). PIP5K1A was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIP5K1A Antibody (A07416-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-ihc-testing-5.jpgAnti-PIP5K1A Antibody Picoband®IHC analysis of PIP5K1A using anti-PIP5K1A antibody (A07416-3). PIP5K1A was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIP5K1A Antibody (A07416-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-ihc-testing-3.jpgAnti-PIP5K1A Antibody Picoband® IHC analysis of PIP5K1A using anti-PIP5K1A antibody (A07416-3). PIP5K1A was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PIP5K1A Antibody (A07416-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-if-testing-4.jpgAnti-PIP5K1A Antibody Picoband® IF analysis of PIP5K1A using anti-PIP5K1A antibody (A07416-3) and anti-Beta Tubulin antibody (M01857-3). PIP5K1A was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PIP5K1A Antibody (A07416-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-ip-testing-5.jpgAnti-PIP5K1A Antibody Picoband® Immunoprecipitating PIP5K1A in 293T whole cell lysate. Western blot analysis of PIP5K1A using anti-PIP5K1A antibody (A07416-3). Lane 1: 293T whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-PIP5K1A antibody in 293T whole cell lysate, Lane 3: anti-PIP5K1A antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PIP5K1A antigen affinity purified polyclonal antibody (A07416-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for PIP5K1A at approximately 63 kDa. The expected band size for PIP5K1A is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07416-3-pip5k1a-primary-antibodies-fcm-testing-6.jpgAnti-PIP5K1A Antibody Picoband® Flow Cytometry analysis of HeLa cells using anti-PIP5K1A antibody (A07416-3). Overlay histogram showing HeLa cells stained with A07416-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PIP5K1A Antibody (A07416-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262082026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262092026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262102026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11712-1-tmem175-primary-antibodies-wb-testing-1.jpgAnti-TMEM175 Antibody Picoband®Western blot analysis of TMEM175 using anti-TMEM175 antibody (A11712-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse testis tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TMEM175 antigen affinity purified polyclonal antibody (A11712-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TMEM175 at approximately 41 kDa. The expected band size for TMEM175 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11712-1-tmem175-primary-antibodies-ihc-testing-1.jpgAnti-TMEM175 Antibody Picoband®IHC analysis of TMEM175 using anti-TMEM175 antibody (A11712-1). TMEM175 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TMEM175 Antibody (A11712-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11712-1-tmem175-primary-antibodies-ihc-testing-2.jpgAnti-TMEM175 Antibody Picoband®IHC analysis of TMEM175 using anti-TMEM175 antibody (A11712-1). TMEM175 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TMEM175 Antibody (A11712-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11712-1-tmem175-primary-antibodies-ihc-testing-3.jpgAnti-TMEM175 Antibody Picoband®IHC analysis of TMEM175 using anti-TMEM175 antibody (A11712-1). TMEM175 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TMEM175 Antibody (A11712-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11712-1-tmem175-primary-antibodies-fcm-testing-1.jpgAnti-TMEM175 Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-TMEM175 antibody (A11712-1). Overlay histogram showing HepG2 cells stained with A11712-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TMEM175 Antibody (A11712-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262112026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262122026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262132026-03-13T05:05:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02575-1-bhlhe40-primary-antibodies-wb-testing-1.jpgAnti-SHARP2/BHLHE40 antibody Western blot analysis of SHARP2/BHLHE40 using anti-SHARP2/BHLHE40 antibody (A02575-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHARP2/BHLHE40 antigen affinity purified polyclonal antibody (A02575-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SHARP2/BHLHE40 at approximately 46 kDa. The expected band size for SHARP2/BHLHE40 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02575-1-bhlhe40-primary-antibodies-ihc-testing-2.jpgAnti-SHARP2/BHLHE40 antibody IHC analysis of SHARP2/BHLHE40 using anti-SHARP2/BHLHE40 antibody (A02575-1). SHARP2/BHLHE40 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-SHARP2/BHLHE40 Antibody (A02575-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02575-1-bhlhe40-primary-antibodies-ihc-testing-3.jpgAnti-SHARP2/BHLHE40 antibody IHC analysis of SHARP2/BHLHE40 using anti-SHARP2/BHLHE40 antibody (A02575-1). SHARP2/BHLHE40 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-SHARP2/BHLHE40 Antibody (A02575-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262142026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02254-3-folr1-primary-antibodies-wb-testing-1.jpgAnti-FOLR1 antibodyWestern blot analysis of FOLR1 using anti-FOLR1 antibody (A02254-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FOLR1 antigen affinity purified polyclonal antibody (A02254-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FOLR1 at approximately 38 kDa. The expected band size for FOLR1 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02254-3-folr1-primary-antibodies-ihc-testing-1.jpgAnti-FOLR1 antibodyIHC analysis of FOLR1 using anti-FOLR1 antibody (A02254-3). FOLR1 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOLR1 Antibody (A02254-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02254-3-folr1-primary-antibodies-ihc-testing-2.jpgAnti-FOLR1 antibodyIHC analysis of FOLR1 using anti-FOLR1 antibody (A02254-3). FOLR1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOLR1 Antibody (A02254-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02254-3-folr1-primary-antibodies-ihc-testing-3.jpgAnti-FOLR1 antibodyIHC analysis of FOLR1 using anti-FOLR1 antibody (A02254-3). FOLR1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOLR1 Antibody (A02254-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02254-3-folr1-primary-antibodies-ihc-testing-4.jpgAnti-FOLR1 antibodyIHC analysis of FOLR1 using anti-FOLR1 antibody (A02254-3). FOLR1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-FOLR1 Antibody (A02254-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262152026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262162026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262172026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262182026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262192026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05464-pgam5-primary-antibodies-wb-testing-1_1.jpgAnti-PGAM5 Antibody Picoband®Western blot analysis of PGAM5 using anti-PGAM5 antibody (A05464). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PGAM5 antigen affinity purified polyclonal antibody (A05464) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PGAM5 at approximately 32 kDa. The expected band size for PGAM5 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05464-pgam5-primary-antibodies-ihc-testing-1.jpgAnti-PGAM5 Antibody Picoband®IHC analysis of PGAM5 using anti-PGAM5 antibody (A05464). PGAM5 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PGAM5 Antibody (A05464) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05464-pgam5-primary-antibodies-ihc-testing-2_1.jpgAnti-PGAM5 Antibody Picoband®IHC analysis of PGAM5 using anti-PGAM5 antibody (A05464). PGAM5 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PGAM5 Antibody (A05464) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05464-pgam5-primary-antibodies-if-testing-1_1.jpgAnti-PGAM5 Antibody Picoband®IF analysis of PGAM5 using anti-PGAM5 antibody (A05464) and anti-Alpha Tubulin antibody (M03989-3). PGAM5 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PGAM5 Antibody (A05464) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05464-pgam5-primary-antibodies-fcm-testing-1.jpgAnti-PGAM5 Antibody Picoband®Flow Cytometry analysis of A549 cells using anti-PGAM5 antibody (A05464). Overlay histogram showing A549 cells stained with A05464 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PGAM5 Antibody (A05464, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262202026-03-13T05:05:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00824-1-rpe65-primary-antibodies-ihc-testing-1.jpgAnti-RPE65 antibody IHC analysis of RPE65 using anti-RPE65 antibody (A00824-1). RPE65 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPE65 Antibody (A00824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00824-1-rpe65-primary-antibodies-ihc-testing-2.jpgAnti-RPE65 antibody IHC analysis of RPE65 using anti-RPE65 antibody (A00824-1). RPE65 was detected in a paraffin-embedded section of mouse eye tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPE65 Antibody (A00824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00824-1-rpe65-primary-antibodies-ihc-testing-3.jpgAnti-RPE65 antibody IHC analysis of RPE65 using anti-RPE65 antibody (A00824-1). RPE65 was detected in a paraffin-embedded section of rat eye tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-RPE65 Antibody (A00824-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262212026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262222026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262232026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262242026-03-16T05:08:30+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262252026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01770-2-ercc5-primary-antibodies-wb-testing-1.jpgAnti-XPG/ERCC5 Antibody Picoband®Western blot analysis of ERCC5 using anti-ERCC5 antibody (A01770-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat C6 tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Neuro-2a tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ERCC5 antigen affinity purified polyclonal antibody (A01770-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ERCC5 at approximately 200 kDa. The expected band size for ERCC5 is at 133 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01770-2-ercc5-primary-antibodies-ihc-testing-1.jpgAnti-XPG/ERCC5 Antibody Picoband®IHC analysis of ERCC5 using anti-ERCC5 antibody (A01770-2). ERCC5 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERCC5 Antibody (A01770-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01770-2-ercc5-primary-antibodies-ihc-testing-2.jpgAnti-XPG/ERCC5 Antibody Picoband®IHC analysis of ERCC5 using anti-ERCC5 antibody (A01770-2). ERCC5 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ERCC5 Antibody (A01770-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01770-2-ercc5-primary-antibodies-if-testing-1.jpgAnti-XPG/ERCC5 Antibody Picoband®IF analysis of ERCC5 using anti-ERCC5 antibody (A01770-2). ERCC5 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ERCC5 Antibody (A01770-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01770-2-ercc5-primary-antibodies-if-testing-2.jpgAnti-XPG/ERCC5 Antibody Picoband®IF analysis of ERCC5 using anti-ERCC5 antibody (A01770-2) and anti-Beta Tubulin antibody (M01857-3). ERCC5 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ERCC5 Antibody (A01770-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01770-2-ercc5-primary-antibodies-fcm-testing-1.jpgAnti-XPG/ERCC5 Antibody Picoband®Flow Cytometry analysis of K562 cells using anti-ERCC5 antibody (A01770-2). Overlay histogram showing K562 cells stained with A01770-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ERCC5 Antibody (A01770-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262262026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262272026-04-02T05:00:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09965-1-chchd6-primary-antibodies-wb-testing-1.jpgAnti-CHCHD6 Antibody Picoband®Western blot analysis of CHCHD6 using anti-CHCHD6 antibody (A09965-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHCHD6 antigen affinity purified polyclonal antibody (A09965-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHCHD6 at approximately 26-29 kDa. The expected band size for CHCHD6 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09965-1-chchd6-primary-antibodies-if-testing-1.jpgAnti-CHCHD6 Antibody Picoband®IF analysis of CHCHD6 using anti-CHCHD6 antibody (A09965-1) and anti-Alpha Tubulin antibody (M03989-3). CHCHD6 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CHCHD6 Antibody (A09965-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09965-1-chchd6-primary-antibodies-fcm-testing-1.jpgAnti-CHCHD6 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-CHCHD6 antibody (A09965-1). Overlay histogram showing Jurkat cells stained with A09965-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHCHD6 Antibody (A09965-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262282026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262292026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01369-1-dystroglycan-dag1-primary-antibodies-wb-testing-1.jpgAnti-Dystroglycan/DAG1 antibody Western blot analysis of Dystroglycan/DAG1 using anti-Dystroglycan/DAG1 antibody (A01369-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Dystroglycan/DAG1 antigen affinity purified polyclonal antibody (A01369-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Dystroglycan/DAG1 at approximately 41 kDa. The expected band size for Dystroglycan/DAG1 is at 97 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01369-1-dag1-primary-antibodies-ihc-testing-1.jpgAnti-Dystroglycan/DAG1 antibodyIHC analysis of Dystroglycan/DAG1 using anti-Dystroglycan/DAG1 antibody (A01369-1). Dystroglycan/DAG1 was detected in a paraffin-embedded section of human brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Dystroglycan/DAG1 Antibody (A01369-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262302026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262312026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262322026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262332026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11591-1-ipo4-primary-antibodies-wb-testing-1.jpgAnti-IPO4 Antibody Picoband®Western blot analysis of IPO4 using anti-IPO4 antibody (A11591-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IPO4 antigen affinity purified polyclonal antibody (A11591-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for IPO4 at approximately 130 kDa. The expected band size for IPO4 is at 119 kDa. https://www.bosterbio.com/catalog/product/view/id/1262342026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262352026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262362026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-wb-testing-1.jpgAnti-NASP antibody Picoband®Western blot analysis of NASP using anti-NASP antibody (A05383-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human A562 whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human THP-1 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NASP antigen affinity purified polyclonal antibody (A05383-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NASP at approximately 150 kDa. The expected band size for NASP is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-ihc-testing-1.jpgAnti-NASP antibody Picoband®IHC analysis of NASP using anti-NASP antibody (A05383-1). NASP was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NASP Antibody (A05383-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-ihc-testing-2.jpgAnti-NASP antibody Picoband®IHC analysis of NASP using anti-NASP antibody (A05383-1). NASP was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NASP Antibody (A05383-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-ihc-testing-3.jpgAnti-NASP antibody Picoband®IHC analysis of NASP using anti-NASP antibody (A05383-1). NASP was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NASP Antibody (A05383-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-if-testing-1.jpgAnti-NASP antibody Picoband®IF analysis of NASP using anti-NASP antibody (A05383-1) and anti-Tubulin Alpha antibody (M03989-3). NASP was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NASP Antibody (A05383-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-if-testing-2.jpgAnti-NASP antibody Picoband®IF analysis of NASP using anti-NASP antibody (A05383-1). NASP was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NASP Antibody (A05383-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-if-testing-3.jpgAnti-NASP antibody Picoband®IF analysis of NASP using anti-NASP antibody (A05383-1). NASP was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-NASP Antibody (A05383-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05383-1-nasp-primary-antibodies-fcm-testing-1.jpgAnti-NASP antibody Picoband®Flow Cytometry analysis of 293T cells using anti-NASP antibody (A05383-1). Overlay histogram showing 293T cells stained with A05383-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NASP Antibody (A05383-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262372026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08638-2-ndufb11-primary-antibodies-wb-testing-1.jpgAnti-NDUFB11 Antibody Picoband®Western blot analysis of NDUFB11 using anti-NDUFB11 antibody (A08638-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat skeletal muscle tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse skeletal muscle tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFB11 antigen affinity purified polyclonal antibody (A08638-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NDUFB11 at approximately 18 kDa. The expected band size for NDUFB11 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08638-2-ndufb11-primary-antibodies-wb-testing-1_1.jpgAnti-NDUFB11 Antibody Picoband®Western blot analysis of NDUFB11 using anti-NDUFB11 antibody (A08638-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NDUFB11 antigen affinity purified polyclonal antibody (A08638-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NDUFB11 at approximately 18 kDa. The expected band size for NDUFB11 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08638-2-ndufb11-primary-antibodies-ihc-testing-1.jpgAnti-NDUFB11 Antibody Picoband®IHC analysis of NDUFB11 using anti-NDUFB11 antibody (A08638-2). NDUFB11 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFB11 Antibody (A08638-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08638-2-ndufb11-primary-antibodies-ihc-testing-2.jpgAnti-NDUFB11 Antibody Picoband®IHC analysis of NDUFB11 using anti-NDUFB11 antibody (A08638-2). NDUFB11 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NDUFB11 Antibody (A08638-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08638-2-ndufb11-primary-antibodies-if-testing-1.jpgAnti-NDUFB11 Antibody Picoband®IF analysis of NDUFB11 using anti-NDUFB11 antibody (A08638-2). NDUFB11 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NDUFB11 Antibody (A08638-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1262382026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05091-1-psma7-primary-antibodies-wb-testing-1.jpgAnti-PSMA7 Antibody Picoband®Western blot analysis of PSMA7 using anti-PSMA7 antibody (A05091-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSMA7 antigen affinity purified polyclonal antibody (A05091-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PSMA7 at approximately 27 kDa. The expected band size for PSMA7 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05091-1-psma7-primary-antibodies-if-testing-1.jpgAnti-PSMA7 Antibody Picoband®IF analysis of PSMA7 using anti-PSMA7 antibody (A05091-1). PSMA7 was detected in a paraffin-embedded section of U2OS tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PSMA7 Antibody (A05091-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05091-1-psma7-primary-antibodies-fcm-testing-1.jpgAnti-PSMA7 Antibody Picoband®Flow Cytometry analysis of HeLa cells using anti-PSMA7 antibody (A05091-1). Overlay histogram showing HeLa cells stained with A05091-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSMA7 Antibody (A05091-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262392026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262402026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262412026-03-16T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-fimmu-08-02013-g001.jpgAnti-SYNJ2BP antibodyDeficiency of omp25 enhances B. suis -induced tumor necrosis factor (TNF)-α production in porcine alveolar macrophages (PAMs) and RAW264.7 cells. (A,B) PAMs and RAW264.7 cells were infected with wild-type (WT) B. suis , Omp25-deficient mutant (Δ omp25 B. suis ), Omp31-deficient mutant (Δ omp31 B. suis ) or were uninfected (ctrl), and TNF-α secretion was measured at 24 h post-infection in culture supernatants by enzyme-linked immunosorbent assay (ELISA). (C,D) PAMs and RAW264.7 cells were infected with WT B. suis , Δ omp25 , or Δ omp31 and cultured for 6 h, Q-PCR was used to measure TNF-α mRNAs levels. (E,F) PAMs and RAW264.7 cells were infected with Δ omp25 , the complemented Δ omp25 strain of B. suis (Δ omp25 - omp25 B. suis ), Δ omp31 , or the complemented Δ omp31 strain of B. suis (Δ omp31 - omp31 B. suis ), followed by ELISA detection of TNF-α in culture supernatants. The results are mean ± SEM of three independent experiments. ** P < 0.01 versus WT B. suis - infected cells. ## P < 0.01 versus Δ omp25 B. suis -infected cells. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fimmu.2017.02013/full'>29387067</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-fimmu-08-02013-g002.jpgAnti-SYNJ2BP antibodyOmp25, but not Omp31, inhibits LPS-induced tumor necrosis factor (TNF)-α production in porcine alveolar macrophages (PAMs) and RAW264.7 cells. (A,B) Evaluation of the expression of Omp25 and Omp31 in PAMs and RAW264.7 cells infected with LV-Blank, lentivirus expressing Omp25 (LV-Omp25), or LV-Omp31. PAMs and RAW264.7 cells were, respectively, infected with 100 multiplicities of infection (MOIs) of lentivirus for 24 h, and then treated with or without LPS for 24 h. The expression of protein was detected by western blotting. (C,D) Omp25 inhibits LPS-induced TNF-α production in PAMs and RAW264.7 cells. Cells were infected and expression of TNF-α was detected by enzyme-linked immunosorbent assay in culture supernatants. (E) Omp25 decreases the levels of TNF-α mRNA in LPS-treated PAMs and RAW264.7 cells. Cells were, respectively, infected with 100 MOIs of lentivirus for 24 h and stimulated with LPS for 6 h, Q-PCR was used to measure the levels of TNF-α mRNA. Values are mean ± SEM of three independent experiments. * P < 0.05, ** P < 0.01 versus LV-Blank-infected cells in the same processing. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fimmu.2017.02013/full'>29387067</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-fimmu-08-02013-g003.jpgAnti-SYNJ2BP antibodyOmp25 inhibits the transcriptional expression of tumor necrosis factor (TNF)-α by suppressing NF-κB pathway activation. (A–D) Porcine alveolar macrophages (PAMs) and RAW264.7 cells were, respectively, transfected with pCI-neo, pCI-neo-Omp31, or pCI-neo-Omp25 along with TNF-α or NF-κB luciferase reporter plasmids for 24 h; cells were stimulated with or without LPS for another 24 h, and TNF-α promoter activities (A,B) and the relative transcriptional activities of NF-κB (C,D) were examined. (E,F) PAMs and RAW264.7 cells were infected with 100 multiplicities of infection of LV-Blank, lentivirus expressing Omp25 (LV-Omp25), or LV-Omp31 for 24 h and the expression levels of cytoplasmic p-IκB, IκB, or p65 and nucleoprotein p65 at 0, 0.5, 1, and 3 h following LPS stimulation were determined by western blotting. The results are mean ± SEM of three independent experiments. * P < 0.05 versus LV-Blank-infected cells; # P < 0.05, ## P < 0.01 versus control (Ctrl) for same transfection. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fimmu.2017.02013/full'>29387067</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-fimmu-08-02013-g004.jpgAnti-SYNJ2BP antibodyOmp25 upregulates miR-130a-3p, -146a, -181a, -181b, or -301a-3p in porcine alveolar macrophages (PAMs) and miR-146a, -181a, -181b, -301a-3p, or -351-5p in RAW264.7 cells. (A,B) Expression profiling of microRNAs in Omp25-expressing PAMs and RAW264.7 cells. Quantitative polymerase chain reaction (Q-PCR) assay was used to measure the levels of 17 specific miRNAs normalized by RNU6B at 24 h following infection. (C–H) Q-PCR was used to measure the kinetics of miR-130a-3p, miR-146a, miR-181a, miR-181b, miR-301a-3p, and miR-155 expression in PAMs infected with LV-Blank or lentivirus expressing Omp25 (LV-Omp25). (I–N) Q-PCR was used to measure the kinetics of miR-146a, miR-181a, miR-181b, miR-301a-3p, miR-351-5p, and miR-155 expression in RAW264.7 cells infected with LV-Blank or LV-Omp25. Results are mean ± SEM of three independent experiments. * P < 0.05, ** P < 0.01 versus LV-Blank-infected cells for same miRNAs or same time point. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fimmu.2017.02013/full'>29387067</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-fimmu-08-02013-g006.jpgAnti-SYNJ2BP antibodyOmp25-induced miR-146a and miR-351-5p inhibit the transcriptional expression of tumor necrosis factor (TNF)-α by targeting to TRAF6 and IRAK1. (A,B) Porcine alveolar macrophages (PAMs) and RAW264.7 cells were infected with LV-Blank and lentivirus expressing Omp25 (LV-Omp25), and western blotting was used to determine the expressions of TRAF6, IRAK1, and IRAK2 at 0, 24, and 48 h. (C,D) PAMs and RAW264.7 cells were transfected with anti-miRNA control or indicated anti-miRNAs; then, cells were infected with LV-Blank or LV-Omp25 for 24 h, following LPS stimulation for another 1 h, and cells were lysed and examined for TRAF6, IRAK1, IRAK2, p-IκB, and IκB by western blotting. (E,F) Cells were transfected with anti-miRNA control or indicated anti-miRNAs and then infected with LV-Blank or LV-Omp25 for 24 h; following LPS treatment for 6 h, quantitative polymerase chain reaction was used to measure the level of TNF-α mRNA. The results are mean ± SEM of three independent experiments. * P < 0.05, ** P < 0.01 versus LV-Blank-infected cells; ## P < 0.01 versus LV-Omp25-infected cells with anti-control (Anti-Ctrl). Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fimmu.2017.02013/full'>29387067</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-fimmu-08-02013-g007.jpgAnti-SYNJ2BP antibodymiR-146a, miR-181a, and miR-301a-3p participate in the regulation of tumor necrosis factor (TNF)-α in both porcine alveolar macrophages (PAMs) and RAW264.7 cells, whereas miR-130a-3p and miR-351-5p differentially regulate TNF-α expression in porcine and murine cells. (A,B) PAMs and RAW264.7 cells were transfected with anti-control, or indicated anti-miRNA, or anti-miRNAs mix (4 miRNA inhibitors); then, cells were infected with LV-Blank or lentivirus expressing Omp25 (LV-Omp25) for 24 h, and the levels of TNF-α were measured by enzyme-linked immunosorbent assay. The results are mean ± SEM of three independent experiments. * P < 0.05, ** P < 0.01 versus LV-Blank-infected cells; # P < 0.05, ## P < 0.01 versus LV-Omp25-infected cells with anti-control (Anti-Ctrl); && P < 0.01 versus LV-Omp25-infected cells with anti-mix (Anti-mix). Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fimmu.2017.02013/full'>29387067</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-fimmu-08-02013-g008.jpgAnti-SYNJ2BP antibodyDeficiency of Omp25 decreases B. suis -induced miR-130a-3p, miR-146a, miR-181a, miR-301a-3p, or miR-351-5p whereas inhibition of these miRNAs upregulates tumor necrosis factor (TNF)-α and promotes the intracellular clearance of wild-type (WT). B. suis . (A–D) Porcine alveolar macrophages (PAMs) were infected with WT B. suis or Δ omp25 B. suis for 0, 6, 12, and 24 h, and quantitative polymerase chain reaction (Q-PCR) was used to analyze the levels of indicated miRNAs. (E) PAMs were transfected anti-control or anti-miRNAs mix; cells were infected with WT B. suis for 24 h, and TNF-α production was measured by enzyme-linked immunosorbent assay (ELISA). (F–I) RAW264.7 cells were infected with WT B. suis or Δ omp25 B. suis for 24 h, and cells were harvested to examine the expression of indicated miRNAs by Q-PCR at 0, 6, 12, and 24 h. (J) RAW264.7 cells were treated as in (E) and followed by ELISA measurement of TNF-α in culture supernatants. (K) Cells were transfected with anti-miRNA control or anti-miRNAs mix and infected with WT B. suis for 24 h; following stimulation with LPS for another 24 h, TNF-α production was measured by ELISA. (L) Cells were transfected anti-miRNA control or anti-miRNAs mix; cells were infected with WT B. suis for 48 h and the numbers of viable intracellular bacteria were determined as described in Section “Materials and Methods.” The results are mean ± SEM of three independent experiments. * P < 0.05, ** P < 0.01 versus WT B. suis -infected cells at same time point; ## P < 0.01 versus Anti-Ctrl. Index in PubMed under a CC BY license. PMID: <a href='https://www.frontiersin.org/articles/10.3389/fimmu.2017.02013/full'>29387067</a> https://www.bosterbio.com/catalog/product/view/id/1262422026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262432026-03-17T05:16:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02653-2-tcof1-primary-antibodies-wb-testing-1.jpgAnti-TCOF1 Antibody Picoband®Western blot analysis of TCOF1 using anti-TCOF1 antibody (A02653-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TCOF1 antigen affinity purified polyclonal antibody (A02653-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TCOF1 at approximately 250 kDa. The expected band size for TCOF1 is at 152 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02653-2-tcof1-primary-antibodies-if-testing-1.jpgAnti-TCOF1 Antibody Picoband®IF analysis of TCOF1 using anti-TCOF1 antibody (A02653-2) and anti-Beta Tubulin antibody (M01857-3). TCOF1 was detected in an immunocytochemical section of SIHA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TCOF1 Antibody (A02653-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02653-2-tcof1-primary-antibodies-fcm-testing-1.jpgAnti-TCOF1 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-TCOF1 antibody (A02653-2). Overlay histogram showing Jurkat cells stained with A02653-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TCOF1 Antibody (A02653-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262442026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262452026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03750-1-trim32-primary-antibodies-wb-testing-1.jpgAnti-TRIM32 Antibody Picoband®Western blot analysis of TRIM32 using anti-TRIM32 antibody (A03750-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRIM32 antigen affinity purified polyclonal antibody (A03750-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TRIM32 at approximately 72 kDa. The expected band size for TRIM32 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03750-1-trim32-primary-antibodies-ihc-testing-1.jpgAnti-TRIM32 Antibody Picoband®IHC analysis of TRIM32 using anti-TRIM32 antibody (A03750-1). TRIM32 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM32 Antibody (A03750-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03750-1-trim32-primary-antibodies-ihc-testing-2.jpgAnti-TRIM32 Antibody Picoband®IHC analysis of TRIM32 using anti-TRIM32 antibody (A03750-1). TRIM32 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM32 Antibody (A03750-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03750-1-trim32-primary-antibodies-ihc-testing-3.jpgAnti-TRIM32 Antibody Picoband®IHC analysis of TRIM32 using anti-TRIM32 antibody (A03750-1). TRIM32 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM32 Antibody (A03750-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03750-1-trim32-primary-antibodies-ihc-testing-4.jpgAnti-TRIM32 Antibody Picoband®IHC analysis of TRIM32 using anti-TRIM32 antibody (A03750-1). TRIM32 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TRIM32 Antibody (A03750-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03750-1-trim32-primary-antibodies-fcm-testing-1.jpgAnti-TRIM32 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-TRIM32 antibody (A03750-1). Overlay histogram showing 293T cells stained with A03750-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TRIM32 Antibody (A03750-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03750-1-trim32-primary-antibodies-fcm-testing-2.jpgAnti-TRIM32 Antibody Picoband®Flow Cytometry analysis of RT4 cells using anti-TRIM32 antibody (A03750-1). Overlay histogram showing RT4 cells stained with A03750-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TRIM32 Antibody (A03750-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262462026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262472026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262482026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262492026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262502026-03-16T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06351-2-cops2-primary-antibodies-wb-testing-1.jpgAnti-CSN2/COPS2 antibodyWestern blot analysis of CSN2/COPS2 using anti-CSN2/COPS2 antibody (A06351-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CSN2/COPS2 antigen affinity purified polyclonal antibody (A06351-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CSN2/COPS2 at approximately 52 kDa. The expected band size for CSN2/COPS2 is at 52 kDa. https://www.bosterbio.com/catalog/product/view/id/1262512026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06865-1-cxxc5-primary-antibodies-wb-testing-1.jpgAnti-CXXC5 Antibody Picoband®Western blot analysis of CXXC5 using anti-CXXC5 antibody (A06865-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CXXC5 antigen affinity purified polyclonal antibody (A06865-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CXXC5 at approximately 38 kDa. The expected band size for CXXC5 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06865-1-cxxc5-primary-antibodies-ihc-testing-1.jpgAnti-CXXC5 Antibody Picoband®IHC analysis of CXXC5 using anti-CXXC5 antibody (A06865-1). CXXC5 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CXXC5 Antibody (A06865-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06865-1-cxxc5-primary-antibodies-ihc-testing-2.jpgAnti-CXXC5 Antibody Picoband®IHC analysis of CXXC5 using anti-CXXC5 antibody (A06865-1). CXXC5 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CXXC5 Antibody (A06865-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06865-1-cxxc5-primary-antibodies-fcm-testing-1.jpgAnti-CXXC5 Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-CXXC5 antibody (A06865-1). Overlay histogram showing SH-SY5Y cells stained with A06865-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CXXC5 Antibody (A06865-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262522026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262532026-04-02T05:01:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06835-4-dnajb4-primary-antibodies-wb-testing-1.jpgAnti-DNAJB4 Antibody Picoband®Western blot analysis of DNAJB4 using anti-DNAJB4 antibody (A06835-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human U2OS whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJB4 antigen affinity purified polyclonal antibody (A06835-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNAJB4 at approximately 38 kDa. The expected band size for DNAJB4 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06835-4-dnajb4-primary-antibodies-fcm-testing-1.jpgAnti-DNAJB4 Antibody Picoband®Flow Cytometry analysis of A549 cells using anti-DNAJB4 antibody (A06835-4). Overlay histogram showing A549 cells stained with A06835-4 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-DNAJB4 Antibody (A06835-4, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262542026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01374-2-dopa-decarboxylase-ddc-primary-antibodies-wb-testing-1.jpgAnti-DOPA decarboxylase/DDC Antibody Picoband® Western blot analysis of DOPA decarboxylase/DDC using anti-DOPA decarboxylase/DDC antibody (A01374-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SHSY-5Y whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat NRK whole cell lysates, Lane 5: rat PC-12 whole cell lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DOPA decarboxylase/DDC antigen affinity purified polyclonal antibody (A01374-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DOPA decarboxylase/DDC at approximately 50 kDa. The expected band size for DOPA decarboxylase/DDC is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01374-2-ddc-primary-antibodies-ihc-testing-1.jpgAnti-DOPA decarboxylase/DDC Antibody Picoband®IHC analysis of DOPA decarboxylase/DDC using anti-DOPA decarboxylase/DDC antibody (A01374-2). DOPA decarboxylase/DDC was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DOPA decarboxylase/DDC Antibody (A01374-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01374-2-dopa-decarboxylase-ddc-primary-antibodies-ip-testing-3.jpgAnti-DOPA decarboxylase/DDC Antibody Picoband® Immunoprecipitating (IP) DOPA decarboxylase/DDC in SH-SY5Y whole cell lysate. Western blot analysis of DOPA decarboxylase/DDC using anti-DOPA decarboxylase/DDC antibody (A01374-2); Lane 1: SH-SY5Y whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-DOPA decarboxylase/DDC antibody in SH-SY5Y whole cell lysate; Lane 3: anti-DOPA decarboxylase/DDC antibody (2μg) + SH-SY5Y whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-DOPA decarboxylase/DDC antigen affinity purified polyclonal antibody (A01374-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for DOPA decarboxylase/DDC at approximately 50 kDa. The expected band size for DOPA decarboxylase/DDC is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01374-2-dopa-decarboxylase-ddc-primary-antibodies-fcm-testing-2.jpgAnti-DOPA decarboxylase/DDC Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-DOPA decarboxylase/DDC antibody (A01374-2). Overlay histogram showing HepG2 cells stained with A01374-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DOPA decarboxylase/DDC Antibody (A01374-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262552026-03-16T05:08:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06214-2-enox2-primary-antibodies-wb-testing-1.jpgAnti-ENOX2 antibody Western blot analysis of ENOX2 using anti-ENOX2 antibody (A06214-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ENOX2 antigen affinity purified polyclonal antibody (A06214-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ENOX2 at approximately 72 kDa. The expected band size for ENOX2 is at 70 kDa. https://www.bosterbio.com/catalog/product/view/id/1262562026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262572026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262582026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262592026-03-16T05:08:31+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262612026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02457-2-pick1-primary-antibodies-wb-testing-1.jpgAnti-PICK1 Antibody Picoband® Western blot analysis of PICK1 using anti-PICK1 antibody (A02457-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PICK1 antigen affinity purified polyclonal antibody (A02457-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PICK1 at approximately 50 kDa. The expected band size for PICK1 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02457-2-pick1-primary-antibodies-ihc-testing-2.jpgAnti-PICK1 Antibody Picoband® IHC analysis of PICK1 using anti-PICK1 antibody (A02457-2). PICK1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PICK1 Antibody (A02457-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02457-2-pick1-primary-antibodies-ihc-testing-3.jpgAnti-PICK1 Antibody Picoband® IHC analysis of PICK1 using anti-PICK1 antibody (A02457-2). PICK1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PICK1 Antibody (A02457-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262622026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10670-2-rab26-primary-antibodies-wb-testing-1.jpgAnti-RAB26 Antibody Picoband®Western blot analysis of RAB26 using anti-RAB26 antibody (A10670-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U-87MG whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB26 antigen affinity purified polyclonal antibody (A10670-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RAB26 at approximately 36 kDa. The expected band size for RAB26 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10670-2-rab26-primary-antibodies-fcm-testing-1.jpgAnti-RAB26 Antibody Picoband®Flow Cytometry analysis of A549 cells using anti-RAB26 antibody (A10670-2). Overlay histogram showing A549 cells stained with A10670-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAB26 Antibody (A10670-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262632026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01310-1-slc30a-primary-antibodies-ihc-testing-1.jpgAnti-ZNT8/SLC30A AntibodyIHC analysis of ZNT8/SLC30A using anti-ZNT8/SLC30A antibody (A01310-1). ZNT8/SLC30A was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ZNT8/SLC30A Antibody (A01310-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01310-1-slc30a-primary-antibodies-if-testing-1.jpgAnti-ZNT8/SLC30A AntibodyIF analysis of ZNT8/SLC30A using anti-ZNT8/SLC30A antibody (A01310-1). ZNT8/SLC30A was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-ZNT8/SLC30A Antibody (A01310-1) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01310-1-slc30a-primary-antibodies-fcm-testing-1.jpgAnti-ZNT8/SLC30A AntibodyFlow Cytometry analysis of Jurkat cells using anti-ZNT8/SLC30A antibody (A01310-1). Overlay histogram showing Jurkat cells stained with A01310-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ZNT8/SLC30A Antibody (A01310-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262642026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262652026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06729-2-sprr3-primary-antibodies-wb-testing-1.jpgAnti-SPRR3 Antibody Picoband® Western blot analysis of SPRR3 using anti-SPRR3 antibody (A06729-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPRR3 antigen affinity purified polyclonal antibody (A06729-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SPRR3 at approximately 24 kDa. The expected band size for SPRR3 is at 19 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06729-2-sprr3-primary-antibodies-wb-testing-1_1.jpgAnti-SPRR3 Antibody Picoband®Western blot analysis of SPRR3 using anti-SPRR3 antibody (A06729-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPRR3 antigen affinity purified polyclonal antibody (A06729-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SPRR3 at approximately 25 kDa. The expected band size for SPRR3 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06729-2-sprr3-primary-antibodies-if-testing-1.jpgAnti-SPRR3 Antibody Picoband®IF analysis of SPRR3 using anti-SPRR3 antibody (A06729-2). SPRR3 was detected in an immunocytochemical section of Caco-2 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SPRR3 Antibody (A06729-2) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1262662026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10056-2-timm50-primary-antibodies-wb-testing-1.jpgAnti-TIMM50 Antibody Picoband®Western blot analysis of TIMM50 using anti-TIMM50 antibody (A10056-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TIMM50 antigen affinity purified polyclonal antibody (A10056-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TIMM50 at approximately 36 kDa. The expected band size for TIMM50 is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10056-2-timm50-primary-antibodies-ihc-testing-1.jpgAnti-TIMM50 Antibody Picoband®IHC analysis of TIMM50 using anti-TIMM50 antibody (A10056-2). TIMM50 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TIMM50 Antibody (A10056-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10056-2-timm50-primary-antibodies-if-testing-1.jpgAnti-TIMM50 Antibody Picoband®IF analysis of TIMM50 using anti-TIMM50 antibody (A10056-2). TIMM50 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TIMM50 Antibody (A10056-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10056-2-timm50-primary-antibodies-fcm-testing-1.jpgAnti-TIMM50 Antibody Picoband®Flow Cytometry analysis of SH-SY5Y cells using anti-TIMM50 antibody (A10056-2). Overlay histogram showing SH-SY5Y cells stained with A10056-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TIMM50 Antibody (A10056-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1262672026-03-16T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08668-1-tom22-tomm22-primary-antibodies-wb-testing-1.jpgAnti-TOM22/TOMM22 antibody Western blot analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (A08668-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TOM22/TOMM22 antigen affinity purified polyclonal antibody (A08668-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TOM22/TOMM22 at approximately 20 kDa. The expected band size for TOM22/TOMM22 is at 15 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08668-1-tom22-tomm22-primary-antibodies-ihc-testing-2.jpgAnti-TOM22/TOMM22 antibody IHC analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (A08668-1). TOM22/TOMM22 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TOM22/TOMM22 Antibody (A08668-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08668-1-tom22-tomm22-primary-antibodies-ihc-testing-3.jpgAnti-TOM22/TOMM22 antibody IHC analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (A08668-1). TOM22/TOMM22 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-TOM22/TOMM22 Antibody (A08668-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08668-1-tom22-tomm22-primary-antibodies-if-testing-1.jpgAnti-TOM22/TOMM22 antibodyIF analysis of TOM22/TOMM22 using anti-TOM22/TOMM22 antibody (A08668-1). TOM22/TOMM22 was detected in an immunocytochemical section of human U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-TOM22/TOMM22 Antibody (A08668-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1262682026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10480-1-uqcrq-primary-antibodies-wb-testing-1.jpgAnti-UQCRQ antibodyWestern blot analysis of UQCRQ using anti-UQCRQ antibody (A10480-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat small intestine tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UQCRQ antigen affinity purified polyclonal antibody (A10480-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UQCRQ at approximately 14 kDa. The expected band size for UQCRQ is at 10 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10480-1-uqcrq-primary-antibodies-ihc-testing-1.jpgAnti-UQCRQ antibodyIHC analysis of UQCRQ using anti-UQCRQ antibody (A10480-1). UQCRQ was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-UQCRQ Antibody (A10480-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10480-1-uqcrq-primary-antibodies-ihc-testing-2.jpgAnti-UQCRQ antibodyIHC analysis of UQCRQ using anti-UQCRQ antibody (A10480-1). UQCRQ was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-UQCRQ Antibody (A10480-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10480-1-uqcrq-primary-antibodies-ihc-testing-3.jpgAnti-UQCRQ antibodyIHC analysis of UQCRQ using anti-UQCRQ antibody (A10480-1). UQCRQ was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-UQCRQ Antibody (A10480-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262692026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262702026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262712026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262722026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262732026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03604-1-arid3a-primary-antibodies-wb-testing-1.jpgAnti-ARID3A Antibody Picoband® Western blot analysis of ARID3A using anti-ARID3A antibody (A03604-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARID3A antigen affinity purified polyclonal antibody (Catalog # A03604-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARID3A at approximately 80 kDa. The expected band size for ARID3A is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03604-1-arid3a-primary-antibodies-fcm-testing-2.jpgAnti-ARID3A Antibody Picoband®Figure2. Flow Cytometry analysis of Caco-2 cells using anti-ARID3A antibody (A03604-1). Overlay histogram showing Caco-2 cells stained with A03604-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARID3A Antibody (A03604-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03604-1-arid3a-primary-antibodies-ip-testing-3.jpgAnti-ARID3A Antibody Picoband® Immunoprecipitating ARID3A in HepG2 whole cell lysate. Western blot analysis of ARID3A using anti-ARID3A antibody (A03604-1). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-ARID3A antibody in HepG2 whole cell lysate, Lane 3: anti-ARID3A antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ARID3A antigen affinity purified polyclonal antibody (A03604-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for ARID3A at approximately 80 kDa. The expected band size for ARID3A is at 63 kDa. https://www.bosterbio.com/catalog/product/view/id/1262742026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01125-2-chd4-primary-antibodies-ihc-testing-1.jpgAnti-CHD4 antibodyIHC analysis of CHD4 using anti-CHD4 antibody (A01125-2). CHD4 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CHD4 Antibody (A01125-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01125-2-chd4-primary-antibodies-ihc-testing-2.jpgAnti-CHD4 antibodyIHC analysis of CHD4 using anti-CHD4 antibody (A01125-2). CHD4 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CHD4 Antibody (A01125-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01125-2-chd4-primary-antibodies-ihc-testing-3.jpgAnti-CHD4 antibodyIHC analysis of CHD4 using anti-CHD4 antibody (A01125-2). CHD4 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CHD4 Antibody (A01125-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01125-2-chd4-primary-antibodies-ihc-testing-4.jpgAnti-CHD4 antibodyIHC analysis of CHD4 using anti-CHD4 antibody (A01125-2). CHD4 was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-CHD4 Antibody (A01125-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262752026-03-13T05:05:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03840-2-elovl4-primary-antibodies-wb-testing-1.jpgAnti-ELOVL4 antibodyWestern blot analysis of ELOVL4 using anti-ELOVL4 antibody (A03840-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Y79 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ELOVL4 antigen affinity purified polyclonal antibody (A03840-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ELOVL4 at approximately 37 kDa. The expected band size for ELOVL4 is at 37 kDa. https://www.bosterbio.com/catalog/product/view/id/1262762026-03-13T05:05:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03219-2-fzr1-primary-antibodies-wb-testing-1.jpgAnti-Cdh1/FZR1 antibody Western blot analysis of FZR1 using anti-FZR1 antibody (A03219-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FZR1 antigen affinity purified polyclonal antibody (A03219-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FZR1 at approximately 60 kDa. The expected band size for FZR1 is at 55 kDa. https://www.bosterbio.com/catalog/product/view/id/1262772026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02637-1-gpx3-primary-antibodies-wb-testing-1.jpgAnti-GPX3 Antibody Picoband® Western blot analysis of GPX3 using anti-GPX3 antibody (A02637-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GPX3 antigen affinity purified polyclonal antibody (A02637-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GPX3 at approximately 20 kDa. The expected band size for GPX3 is at 26 kDa. https://www.bosterbio.com/catalog/product/view/id/1262782026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262792026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262802026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262812026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262822026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262832026-04-02T05:01:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04311-1-rpl3-primary-antibodies-wb-testing-1.jpgAnti-RPL3 Antibody Picoband® Western blot analysis of RPL3 using anti-RPL3 antibody (A04311-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat PC-12 whole cell lysates, Lane 5: mouse kidney tissue lysates, Lane 6: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPL3 antigen affinity purified polyclonal antibody (A04311-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPL3 at approximately 46 kDa. The expected band size for RPL3 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04311-1-rpl3-primary-antibodies-wb-testing-1_1.jpgAnti-RPL3 Antibody Picoband®Western blot analysis of RPL3 using anti-RPL3 antibody (A04311-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: rat spleen tissue lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPL3 antigen affinity purified polyclonal antibody (A04311-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPL3 at approximately 46 kDa. The expected band size for RPL3 is at 46 kDa. https://www.bosterbio.com/catalog/product/view/id/1262842026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262852026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262862026-03-16T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07855-1-syntaxin-7-stx7-primary-antibodies-wb-testing-1.jpgAnti-Syntaxin 7/STX7 antibody Western blot analysis of Syntaxin 7/STX7 using anti-Syntaxin 7/STX7 antibody (A07855-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat heart tissue lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse heart tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Syntaxin 7/STX7 antigen affinity purified polyclonal antibody (A07855-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Syntaxin 7/STX7 at approximately 37 kDa. The expected band size for Syntaxin 7/STX7 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07855-1-stx7-primary-antibodies-ihc-testing-1.jpgAnti-Syntaxin 7/STX7 antibodyIHC analysis of Syntaxin 7/STX7 using anti-Syntaxin 7/STX7 antibody (A07855-1). Syntaxin 7/STX7 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Syntaxin 7/STX7 Antibody (A07855-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1262872026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07996-1-dnajc7-primary-antibodies-wb-testing-1.jpgAnti-DNAJC7 Antibody Picoband®Western blot analysis of DNAJC7 using anti-DNAJC7 antibody (A07996-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat skeletal muscle tissue lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DNAJC7 antigen affinity purified polyclonal antibody (A07996-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DNAJC7 at approximately 56 kDa. The expected band size for DNAJC7 is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07996-1-dnajc7-primary-antibodies-if-testing-1.jpgAnti-DNAJC7 Antibody Picoband®IF analysis of DNAJC7 using anti-DNAJC7 antibody (A07996-1) and anti-Alpha Tubulin antibody (M03989-3). DNAJC7 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DNAJC7 Antibody (A07996-1) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07996-1-dnajc7-primary-antibodies-ip-testing-1.jpgAnti-DNAJC7 Antibody Picoband®Immunoprecipitating DNAJC7 in A549 whole cell lysate. Western blot analysis of DNAJC7 using anti-DNAJC7 antibody (A07996-1). Lane 1: A549 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-DNAJC7 antibody in A549 whole cell lysate, Lane 3: anti-DNAJC7 antibody (2μg) + A549 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-DNAJC7 antigen affinity purified polyclonal antibody (A07996-1) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for DNAJC7 at approximately 56 kDa. The expected band size for DNAJC7 is at 56 kDa. https://www.bosterbio.com/catalog/product/view/id/1262882026-03-16T05:08:32+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262892026-03-16T05:08:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06303-3-fgl2-primary-antibodies-wb-testing-1.jpgAnti-FGL2 antibody Western blot analysis of FGL2 using anti-FGL2 antibody (A06303-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FGL2 antigen affinity purified polyclonal antibody (A06303-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FGL2 at approximately 85 kDa. The expected band size for FGL2 is at 50 kDa. https://www.bosterbio.com/catalog/product/view/id/1262902026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06856-2-pom121-primary-antibodies-wb-testing-1.jpgAnti-POM121 Antibody Picoband®Western blot analysis of POM121 using anti-POM121 antibody (A06856-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POM121 antigen affinity purified polyclonal antibody (A06856-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for POM121 at approximately 150 kDa. The expected band size for POM121 is at 128 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06856-2-pom121-primary-antibodies-if-testing-1.jpgAnti-POM121 Antibody Picoband®IF analysis of POM121 using anti-POM121 antibody (A06856-2) and anti-Alpha Tubulin antibody (M03989-3). POM121 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POM121 Antibody (A06856-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1262912026-03-13T05:05:07+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262922026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262932026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262942026-03-13T05:05:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02508-1-ubqln2-primary-antibodies-wb-testing-1.jpgAnti-UBQLN2 antibodyWestern blot analysis of UBQLN2 using anti-UBQLN2 antibody (A02508-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-UBQLN2 antigen affinity purified polyclonal antibody (A02508-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for UBQLN2 at approximately 70 kDa. The expected band size for UBQLN2 is at 66 kDa. https://www.bosterbio.com/catalog/product/view/id/1262952026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262962026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262972026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262982026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1262992026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263002026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263012026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-wb-testing-1.jpgAnti-HMGN1 antibodyWestern blot analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HMGN1 antigen affinity purified polyclonal antibody (A03051-3) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for HMGN1 at approximately 19 kDa. The expected band size for HMGN1 is at 11 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-ihc-testing-1.jpgAnti-HMGN1 antibodyIHC analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). HMGN1 was detected in a paraffin-embedded section of human lymphoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HMGN1 Antibody (A03051-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-ihc-testing-2.jpgAnti-HMGN1 antibodyIHC analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). HMGN1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HMGN1 Antibody (A03051-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-ihc-testing-3.jpgAnti-HMGN1 antibodyIHC analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). HMGN1 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HMGN1 Antibody (A03051-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-ihc-testing-4.jpgAnti-HMGN1 antibodyIHC analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). HMGN1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HMGN1 Antibody (A03051-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-ihc-testing-5.jpgAnti-HMGN1 antibodyIHC analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). HMGN1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HMGN1 Antibody (A03051-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-ihc-testing-6.jpgAnti-HMGN1 antibodyIHC analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). HMGN1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HMGN1 Antibody (A03051-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03051-3-hmgn1-primary-antibodies-ihc-testing-7.jpgAnti-HMGN1 antibodyIHC analysis of HMGN1 using anti-HMGN1 antibody (A03051-3). HMGN1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-HMGN1 Antibody (A03051-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263022026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263032026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263042026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07063-1-taok1-primary-antibodies-wb-testing-1.jpgAnti-TAOK1 Antibody Picoband®Western blot analysis of TAOK1 using anti-TAOK1 antibody (A07063-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TAOK1 antigen affinity purified polyclonal antibody (A07063-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TAOK1 at approximately 130 kDa. The expected band size for TAOK1 is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07063-1-taok1-primary-antibodies-ip-testing-1.jpgAnti-TAOK1 Antibody Picoband®Immunoprecipitating TAOK1 in Hela whole cell lysate. Western blot analysis of TAOK1 using anti-TAOK1 antibody (A07063-1). Lane 1: Hela whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-TAOK1 antibody in Hela whole cell lysate, Lane 3: anti-TAOK1 antibody (2μg) + Hela whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TAOK1 antigen affinity purified polyclonal antibody (A07063-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for TAOK1 at approximately 130 kDa. The expected band size for TAOK1 is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07063-1-taok1-primary-antibodies-fcm-testing-1.jpgAnti-TAOK1 Antibody Picoband®Flow Cytometry analysis of HeLa cells using anti-TAOK1 antibody (A07063-1). Overlay histogram showing HeLa cells stained with A07063-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TAOK1 Antibody (A07063-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263052026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07234-3-tmed10-primary-antibodies-wb-testing-1.jpgAnti-TMP21/TMED10 Antibody Picoband®Western blot analysis of TMP21/TMED10 using anti-TMP21/TMED10 antibody (A07234-3). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: rat pancreas tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse pancreas tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TMP21/TMED10 antigen affinity purified polyclonal antibody (A07234-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TMP21/TMED10 at approximately 20 kDa. The expected band size for TMP21/TMED10 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07234-3-tmed10-primary-antibodies-ihc-testing-1.jpgAnti-TMP21/TMED10 Antibody Picoband®IHC analysis of TMP21/TMED10 using anti-TMP21/TMED10 antibody (A07234-3). TMP21/TMED10 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TMP21/TMED10 Antibody (A07234-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07234-3-tmed10-primary-antibodies-ihc-testing-2.jpgAnti-TMP21/TMED10 Antibody Picoband®IHC analysis of TMP21/TMED10 using anti-TMP21/TMED10 antibody (A07234-3). TMP21/TMED10 was detected in a paraffin-embedded section of human parotid gland tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TMP21/TMED10 Antibody (A07234-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07234-3-tmed10-primary-antibodies-if-testing-1.jpgAnti-TMP21/TMED10 Antibody Picoband®IF analysis of TMP21/TMED10 using anti-TMP21/TMED10 antibody (A07234-3). TMP21/TMED10 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TMP21/TMED10 Antibody (A07234-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07234-3-tmed10-primary-antibodies-if-testing-2.jpgAnti-TMP21/TMED10 Antibody Picoband®IF analysis of TMP21/TMED10 using anti-TMP21/TMED10 antibody (A07234-3). TMP21/TMED10 was detected in a paraffin-embedded section of human parotid gland tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-TMP21/TMED10 Antibody (A07234-3) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07234-3-tmed10-primary-antibodies-fcm-testing-1.jpgAnti-TMP21/TMED10 Antibody Picoband®Flow Cytometry analysis of THP-1 cells using anti-TMP21/TMED10 antibody (A07234-3). Overlay histogram showing THP-1 cells stained with A07234-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TMP21/TMED10 Antibody (A07234-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263062026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263072026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263082026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263092026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06012-3-polg2-primary-antibodies-wb-testing-1.jpgAnti-POLG2 Antibody Picoband®Western blot analysis of POLG2 using anti-POLG2 antibody (A06012-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLG2 antigen affinity purified polyclonal antibody (A06012-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for POLG2 at approximately 55 kDa. The expected band size for POLG2 is at 55 kDa. https://www.bosterbio.com/catalog/product/view/id/1263102026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05731-1-ppm1b-primary-antibodies-wb-testing-1.jpgAnti-PPM1B Antibody Picoband® Western blot analysis of PPM1B using anti-PPM1B antibody (A05731-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPM1B antigen affinity purified polyclonal antibody (A05731-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PPM1B at approximately 53 kDa. The expected band size for PPM1B is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05731-1-ppm1b-primary-antibodies-ihc-testing-1.jpgAnti-PPM1B Antibody Picoband®IHC analysis of PPM1B using anti-PPM1B antibody (A05731-1). PPM1B was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PPM1B Antibody (A05731-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05731-1-ppm1b-primary-antibodies-wb-testing-1_1.jpgAnti-PPM1B Antibody Picoband®Western blot analysis of PPM1B using anti-PPM1B antibody (A05731-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat testis tissue lysates Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PPM1B antigen affinity purified polyclonal antibody (A05731-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PPM1B at approximately 53 kDa. The expected band size for PPM1B is at 53 kDa. https://www.bosterbio.com/catalog/product/view/id/1263112026-03-16T05:08:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10452-1-rab37-primary-antibodies-wb-testing-1.jpgAnti-RAB37 antibody Western blot analysis of RAB37 using anti-RAB37 antibody (A10452-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB37 antigen affinity purified polyclonal antibody (A10452-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RAB37 at approximately 25 kDa. The expected band size for RAB37 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10452-1-rab37-primary-antibodies-ihc-testing-1.jpgAnti-RAB37 antibodyIHC analysis of RAB37 using anti-RAB37 antibody (A10452-1). RAB37 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB37 Antibody (A10452-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263122026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263132026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263142026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263152026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263162026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263172026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263182026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263192026-03-13T05:05:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01740-2-dspp-primary-antibodies-wb-testing-1.jpgAnti-DSPP antibody Western blot analysis of DSPP using anti-DSPP antibody (A01740-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DSPP antigen affinity purified polyclonal antibody (A01740-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DSPP at approximately 150 kDa. The expected band size for DSPP is at 131 kDa. https://www.bosterbio.com/catalog/product/view/id/1263202026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263212026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263222026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12808-1-fbxl14-primary-antibodies-wb-testing-1.jpgAnti-FBXL14 Antibody Picoband®Western blot analysis of FBXL14 using anti-FBXL14 antibody (A12808-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human U2OS whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FBXL14 antigen affinity purified polyclonal antibody (A12808-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FBXL14 at approximately 50 kDa. The expected band size for FBXL14 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12808-1-fbxl14-primary-antibodies-if-testing-1.jpgAnti-FBXL14 Antibody Picoband®IF analysis of FBXL14 using anti-FBXL14 antibody (A12808-1). FBXL14 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-FBXL14 Antibody (A12808-1) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1263232026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263242026-03-16T05:08:33+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263252026-03-17T05:16:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02783-1-rxfp1-primary-antibodies-wb-testing-1.jpgAnti-RXFP1 Antibody Picoband®Western blot analysis of RXFP1 using anti-RXFP1 antibody (A02783-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RXFP1 antigen affinity purified polyclonal antibody (A02783-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RXFP1 at approximately 85 kDa. The expected band size for RXFP1 is at 87 kDa. https://www.bosterbio.com/catalog/product/view/id/1263262026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263272026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263282026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263292026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263302026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263312026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263322026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263332026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263342026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263352026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263362026-03-24T05:36:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11205-1-lgtn-primary-antibodies-wb-testing-1.jpgAnti-LGTN/EIF2D antibodyWestern blot analysis of LGTN using anti-LGTN antibody (A11205-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LGTN antigen affinity purified polyclonal antibody (A11205-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LGTN at approximately 70 kDa. The expected band size for LGTN is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11205-1-lgtn-primary-antibodies-ihc-testing-1.jpgAnti-LGTN/EIF2D antibodyIHC analysis of LGTN using anti-LGTN antibody (A11205-1). LGTN was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-LGTN Antibody (A11205-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11205-1-lgtn-primary-antibodies-ihc-testing-2.jpgAnti-LGTN/EIF2D antibodyIHC analysis of LGTN using anti-LGTN antibody (A11205-1). LGTN was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-LGTN Antibody (A11205-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11205-1-lgtn-primary-antibodies-ihc-testing-3.jpgAnti-LGTN/EIF2D antibodyIHC analysis of LGTN using anti-LGTN antibody (A11205-1). LGTN was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-LGTN Antibody (A11205-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263372026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263382026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263392026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263402026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263412026-03-16T05:08:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04795-adcy3-primary-antibodies-wb-testing-1.jpgAnti-ADCY3 antibodyWestern blot analysis of ADCY3 using anti-ADCY3 antibody (A04795). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADCY3 antigen affinity purified polyclonal antibody (A04795) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ADCY3 at approximately 129 kDa. The expected band size for ADCY3 is at 129 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04795-adcy3-primary-antibodies-ihc-testing-1.jpgAnti-ADCY3 antibodyIHC analysis of ADCY3 using anti-ADCY3 antibody (A04795). ADCY3 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-ADCY3 Antibody (A04795) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04795-adcy3-primary-antibodies-if-testing-1.jpgAnti-ADCY3 antibodyIF analysis of ADCY3 using anti-ADCY3 antibody (A04795). ADCY3 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 1:100 rabbit anti-ADCY3 Antibody (A04795) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1263422026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263432026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263442026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263452026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263462026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13540-2-lratd2-primary-antibodies-wb-testing-1.jpgAnti-FAM84B/LRATD2 Antibody Picoband®Western blot analysis of FAM84B/LRATD2 using anti-FAM84B/LRATD2 antibody (A13540-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MDA-MB-453 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAM84B/LRATD2 antigen affinity purified polyclonal antibody (A13540-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FAM84B/LRATD2 at approximately 40 kDa. The expected band size for FAM84B/LRATD2 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13540-2-lratd2-primary-antibodies-ihc-testing-1.jpgAnti-FAM84B/LRATD2 Antibody Picoband®IHC analysis of FAM84B/LRATD2 using anti-FAM84B/LRATD2 antibody (A13540-2). FAM84B/LRATD2 was detected in a paraffin-embedded section of human esophagus cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM84B/LRATD2 Antibody (A13540-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13540-2-lratd2-primary-antibodies-if-testing-1.jpgAnti-FAM84B/LRATD2 Antibody Picoband®IF analysis of FAM84B/LRATD2 using anti-FAM84B/LRATD2 antibody (A13540-2) and anti-Alpha Tubulin antibody (M03989-3). FAM84B/LRATD2 was detected in an immunocytochemical section of A431 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-FAM84B/LRATD2 Antibody (A13540-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1263472026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04399-2-sik1-primary-antibodies-wb-testing-1.jpgAnti-Snf1lk/SIK1 Antibody Picoband®Western blot analysis of SIK1 using anti-SIK1 antibody (A04399-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat spleen tissue lysates, Lane 7: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SIK1 antigen affinity purified polyclonal antibody (A04399-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SIK1 at approximately 85 kDa. The expected band size for SIK1 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04399-2-sik1-primary-antibodies-if-testing-1.jpgAnti-Snf1lk/SIK1 Antibody Picoband®IF analysis of SIK1 using anti-SIK1 antibody (A04399-2) and anti-Beta Tubulin antibody (M01857-3). SIK1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SIK1 Antibody (A04399-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04399-2-sik1-primary-antibodies-fcm-testing-1.jpgAnti-Snf1lk/SIK1 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-SIK1 antibody (A04399-2). Overlay histogram showing Jurkat cells stained with A04399-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SIK1 Antibody (A04399-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263482026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263492026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263502026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263512026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263522026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263532026-03-16T05:08:34+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263542026-03-16T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05138-4-asbt-primary-antibodies-wb-testing-1.jpgAnti-ASBT antibodyWestern blot analysis of ASBT using anti-ASBT antibody (A05138-4). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ASBT antigen affinity purified polyclonal antibody (A05138-4) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ASBT at approximately 38-40 kDa. The expected band size for ASBT is at 38 kDa. https://www.bosterbio.com/catalog/product/view/id/1263552026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263562026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263572026-04-02T05:01:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04340-2-etfdh-primary-antibodies-wb-testing-1.jpgAnti-ETFDH Antibody Picoband®Western blot analysis of ETFDH using anti-ETFDH antibody (A04340-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: rat kidney tissue lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse kidney tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ETFDH antigen affinity purified polyclonal antibody (A04340-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ETFDH at approximately 68 kDa. The expected band size for ETFDH is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04340-2-etfdh-primary-antibodies-fcm-testing-1.jpgAnti-ETFDH Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-ETFDH antibody (A04340-2). Overlay histogram showing Jurkat cells stained with A04340-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ETFDH Antibody (A04340-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263582026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08797-2-faf2-primary-antibodies-wb-testing-1.jpgAnti-FAF2 Antibody Picoband®Western blot analysis of FAF2 using anti-FAF2 antibody (A08797-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAF2 antigen affinity purified polyclonal antibody (A08797-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FAF2 at approximately 53 kDa. The expected band size for FAF2 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08797-2-faf2-primary-antibodies-ihc-testing-1.jpgAnti-FAF2 Antibody Picoband®IHC analysis of FAF2 using anti-FAF2 antibody (A08797-2). FAF2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAF2 Antibody (A08797-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08797-2-faf2-primary-antibodies-ihc-testing-2.jpgAnti-FAF2 Antibody Picoband®IHC analysis of FAF2 using anti-FAF2 antibody (A08797-2). FAF2 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAF2 Antibody (A08797-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08797-2-faf2-primary-antibodies-ihc-testing-3.jpgAnti-FAF2 Antibody Picoband®IHC analysis of FAF2 using anti-FAF2 antibody (A08797-2). FAF2 was detected in a paraffin-embedded section of human testicular cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAF2 Antibody (A08797-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08797-2-faf2-primary-antibodies-ip-testing-1.jpgAnti-FAF2 Antibody Picoband®Immunoprecipitating FAF2 in K562 whole cell lysate. Western blot analysis of FAF2 using anti-FAF2 antibody (A08797-2). Lane 1: K562 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-FAF2 antibody in K562 whole cell lysate, Lane 3: anti-FAF2 antibody (2μg) + K562 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FAF2 antigen affinity purified polyclonal antibody (A08797-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for FAF2 at approximately 53 kDa. The expected band size for FAF2 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08797-2-faf2-primary-antibodies-fcm-testing-1.jpgAnti-FAF2 Antibody Picoband®Flow Cytometry analysis of 293T cells using anti-FAF2 antibody (A08797-2). Overlay histogram showing 293T cells stained with A08797-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FAF2 Antibody (A08797-2, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263592026-03-16T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07281-2-spin1-primary-antibodies-wb-testing-1.jpgAnti-SPIN1 antibodyWestern blot analysis of SPIN1 using anti-SPIN1 antibody (A07281-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human OVCAR-8 whole cell lysates, Lane 4: human OVCAR-8 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SPIN1 antigen affinity purified polyclonal antibody (A07281-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SPIN1 at approximately 30 kDa. The expected band size for SPIN1 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07281-2-spin1-primary-antibodies-ihc-testing-1.jpgAnti-SPIN1 antibodyIHC analysis of SPIN1 using anti-SPIN1 antibody (A07281-2). SPIN1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:200 rabbit anti-SPIN1 Antibody (A07281-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263602026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263612026-04-03T05:00:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09017-2-chac1-primary-antibodies-wb-testing-1.jpgAnti-CHAC1 Antibody Picoband® Western blot analysis of CHAC1 using anti-CHAC1 antibody (A09017-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHAC1 antigen affinity purified polyclonal antibody (A09017-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHAC1 at approximately 40 kDa. The expected band size for CHAC1 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09017-2-chac1-primary-antibodies-ihc-testing-1.jpgAnti-CHAC1 Antibody Picoband®IHC analysis of CHAC1 using anti-CHAC1 antibody (A09017-2). CHAC1 was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHAC1 Antibody (A09017-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09017-2-chac1-primary-antibodies-wb-testing-1_1.jpgAnti-CHAC1 Antibody Picoband®Western blot analysis of CHAC1 using anti-CHAC1 antibody (A09017-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human U2OS whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHAC1 antigen affinity purified polyclonal antibody (A09017-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CHAC1 at approximately 42 kDa. The expected band size for CHAC1 is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09017-2-chac1-primary-antibodies-ihc-testing-1_1.jpgAnti-CHAC1 Antibody Picoband®IHC analysis of CHAC1 using anti-CHAC1 antibody (A09017-2). CHAC1 was detected in a paraffin-embedded section of human pancrease tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CHAC1 Antibody (A09017-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263622026-03-13T05:05:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03010-2-drd5-primary-antibodies-wb-testing-1.jpgAnti-DRD5 antibodyWestern blot analysis of DRD5 using anti-DRD5 antibody (A03010-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DRD5 antigen affinity purified polyclonal antibody (A03010-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DRD5 at approximately 50 kDa. The expected band size for DRD5 is at 53 kDa. https://www.bosterbio.com/catalog/product/view/id/1263632026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263642026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263652026-04-02T05:01:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06320-1-eif2b4-primary-antibodies-wb-testing-1.jpgAnti-EIF2B4 Antibody Picoband®Western blot analysis of EIF2B4 using anti-EIF2B4 antibody (A06320-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF2B4 antigen affinity purified polyclonal antibody (A06320-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EIF2B4 at approximately 58 kDa. The expected band size for EIF2B4 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06320-1-eif2b4-primary-antibodies-ip-testing-1.jpgAnti-EIF2B4 Antibody Picoband®Immunoprecipitating EIF2B4 in K562 whole cell lysate. Western blot analysis of EIF2B4 using anti-EIF2B4 antibody (A06320-1). Lane 1: K562 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-EIF2B4 antibody in K562 whole cell lysate, Lane 3: anti-EIF2B4 antibody (2μg) + K562 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-EIF2B4 antigen affinity purified polyclonal antibody (A06320-1) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Catalog # BM2007). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for EIF2B4 at approximately 58 kDa. The expected band size for EIF2B4 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06320-1-eif2b4-primary-antibodies-fcm-testing-1.jpgAnti-EIF2B4 Antibody Picoband®Flow Cytometry analysis of K562 cells using anti-EIF2B4 antibody (A06320-1). Overlay histogram showing K562 cells stained with A06320-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EIF2B4 Antibody (A06320-1, 1 μg/1x106 cells) for 30 min at 20°C. Fluoro488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263662026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263672026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263682026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06497-2-gtse1-primary-antibodies-wb-testing-1.jpgAnti-GTSE1 Antibody Picoband®Western blot analysis of GTSE1 using anti-GTSE1 antibody (A06497-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U2OS whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GTSE1 antigen affinity purified polyclonal antibody (A06497-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GTSE1 at approximately 100 kDa. The expected band size for GTSE1 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06497-2-gtse1-primary-antibodies-ihc-testing-1.jpgAnti-GTSE1 Antibody Picoband®IHC analysis of GTSE1 using anti-GTSE1 antibody (A06497-2). GTSE1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GTSE1 Antibody (A06497-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06497-2-gtse1-primary-antibodies-ihc-testing-2.jpgAnti-GTSE1 Antibody Picoband®IHC analysis of GTSE1 using anti-GTSE1 antibody (A06497-2). GTSE1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GTSE1 Antibody (A06497-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263692026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263702026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263712026-03-16T05:08:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04836-2-pdhx-primary-antibodies-wb-testing-1.jpgAnti-PDHX antibodyWestern blot analysis of PDHX using anti-PDHX antibody (A04836-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SK-OV-3 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDHX antigen affinity purified polyclonal antibody (A04836-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PDHX at approximately 54 kDa. The expected band size for PDHX is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04836-2-pdhx-primary-antibodies-ihc-testing-1.jpgAnti-PDHX antibodyIHC analysis of PDHX using anti-PDHX antibody (A04836-2). PDHX was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:50 rabbit anti-PDHX Antibody (A04836-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263722026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263732026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03530-2-pik3c2a-primary-antibodies-wb-testing-1.jpgAnti-PIK3C2A Antibody Picoband®Western blot analysis of PIK3C2A using anti-PIK3C2A antibody (A03530-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIK3C2A antigen affinity purified polyclonal antibody (A03530-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PIK3C2A at approximately 191 kDa. The expected band size for PIK3C2A is at 191 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03530-2-pik3c2a-primary-antibodies-if-testing-1.jpgAnti-PIK3C2A Antibody Picoband®IF analysis of PIK3C2A using anti-PIK3C2A antibody (A03530-2). PIK3C2A was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PIK3C2A Antibody (A03530-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1263742026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-wb-testing-1.jpgAnti-QKI Antibody Picoband®Western blot analysis of QKI using anti-QKI antibody (A01874-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SK-OV-3 whole cell lysates, Lane 2: monkey Cos-7 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-QKI antigen affinity purified polyclonal antibody (A01874-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for QKI at approximately 38 kDa. The expected band size for QKI is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-ihc-testing-1.jpgAnti-QKI Antibody Picoband®IHC analysis of QKI using anti-QKI antibody (A01874-3). QKI was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-QKI Antibody (A01874-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-ihc-testing-2.jpgAnti-QKI Antibody Picoband®IHC analysis of QKI using anti-QKI antibody (A01874-3). QKI was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-QKI Antibody (A01874-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-ihc-testing-3.jpgAnti-QKI Antibody Picoband®IHC analysis of QKI using anti-QKI antibody (A01874-3). QKI was detected in a paraffin-embedded section of human renal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-QKI Antibody (A01874-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-ihc-testing-4.jpgAnti-QKI Antibody Picoband®IHC analysis of QKI using anti-QKI antibody (A01874-3). QKI was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-QKI Antibody (A01874-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-ihc-testing-5.jpgAnti-QKI Antibody Picoband®IHC analysis of QKI using anti-QKI antibody (A01874-3). QKI was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-QKI Antibody (A01874-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-ihc-testing-6.jpgAnti-QKI Antibody Picoband®IHC analysis of QKI using anti-QKI antibody (A01874-3). QKI was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-QKI Antibody (A01874-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-if-testing-1.jpgAnti-QKI Antibody Picoband®IF analysis of QKI using anti-QKI antibody (A01874-3) and anti-Beta Tubulin antibody (M01857-3). QKI was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-QKI Antibody (A01874-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-ip-testing-1.jpgAnti-QKI Antibody Picoband®Immunoprecipitating QKI in K562 whole cell lysate. Western blot analysis of QKI using anti-QKI antibody (A01874-3). Lane 1: K562 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-QKI antibody in K562 whole cell lysate, Lane 3: anti-QKI antibody (2μg) + K562 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-QKI antigen affinity purified polyclonal antibody (A01874-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for QKI at approximately 38 kDa. The expected band size for QKI is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-fcm-testing-1.jpgAnti-QKI Antibody Picoband®Flow Cytometry analysis of Neuro-2a cells using anti-QKI antibody (A01874-3). Overlay histogram showing Neuro-2a cells stained with A01874-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-QKI Antibody (A01874-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01874-3-qki-primary-antibodies-fcm-testing-2.jpgAnti-QKI Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-QKI antibody (A01874-3). Overlay histogram showing U251 cells stained with A01874-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-QKI Antibody (A01874-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263752026-03-16T05:08:35+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263762026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263772026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263782026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01122-sln-primary-antibodies-ihc-testing-1.jpgAnti-SLN AntibodyIHC analysis of SLN using anti-SLN antibody (A01122). SLN was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLN Antibody (A01122) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01122-sln-primary-antibodies-ihc-testing-2.jpgAnti-SLN AntibodyIHC analysis of SLN using anti-SLN antibody (A01122). SLN was detected in a paraffin-embedded section of rat skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLN Antibody (A01122) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01122-sln-primary-antibodies-ihc-testing-3.jpgAnti-SLN AntibodyIHC analysis of SLN using anti-SLN antibody (A01122). SLN was detected in a paraffin-embedded section of mouse skeletal muscle tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLN Antibody (A01122) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263792026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263802026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263812026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263822026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263832026-03-13T05:05:08+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263842026-03-13T05:05:09+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263852026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263862026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263872026-03-16T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05932-bbs7-primary-antibodies-ihc-testing-1.jpgAnti-BBS7 antibodyIHC analysis of BBS7 using anti-BBS7 antibody (A05932). BBS7 was detected in a paraffin-embedded section of human fallopian tube tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 200 rabbit anti-BBS7 Antibody (A05932) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05932-bbs7-primary-antibodies-ihc-testing-2.jpgAnti-BBS7 antibodyIHC analysis of BBS7 using anti-BBS7 antibody (A05932). BBS7 was detected in a paraffin-embedded section of human fallopian tube tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 200 rabbit anti-BBS7 Antibody (A05932) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263882026-03-13T05:05:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03575-1-ark5-primary-antibodies-wb-testing-1.jpgAnti-ARK5/NUAK1 antibodyWestern blot analysis of ARK5/NUAK1 using anti-ARK5/NUAK1 antibody (A03575-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARK5/NUAK1 antigen affinity purified monoclonal antibody (A03575-1) at 1:500 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ARK5/NUAK1 at approximately 74 kDa. The expected band size for ARK5/NUAK1 is at 74 kDa. https://www.bosterbio.com/catalog/product/view/id/1263892026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04155-1-arl2-primary-antibodies-wb-testing-1.jpgAnti-ARL2 Antibody Picoband® Western blot analysis of ARL2 using anti-ARL2 antibody (A04155-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human T-47D whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human U-397 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARL2 antigen affinity purified polyclonal antibody (Catalog # A04155-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARL2 at approximately 18 kDa. The expected band size for ARL2 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04155-1-arl2-primary-antibodies-ihc-testing-2.jpgAnti-ARL2 Antibody Picoband® IHC analysis of ARL2 using anti-ARL2 antibody (A04155-1). ARL2 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ARL2 Antibody (A04155-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04155-1-arl2-primary-antibodies-if-testing-3.jpgAnti-ARL2 Antibody Picoband® IF analysis of ARL2 using anti-ARL2 antibody (A04155-1). ARL2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ARL2 Antibody (A04155-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04155-1-arl2-primary-antibodies-fcm-testing-4.jpgAnti-ARL2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-ARL2 antibody (A04155-1). Overlay histogram showing JK cells stained with A04155-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ARL2 Antibody (A04155-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1263902026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263912026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263922026-03-16T05:08:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09088-2-atad3a-b-primary-antibodies-wb-testing-1.jpgAnti-ATAD3A/B antibodyWestern blot analysis of ATAD3A/B using anti-ATAD3A/B antibody (A09088-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse liver tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATAD3A/B antigen affinity purified polyclonal antibody (A09088-2) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:1000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ATAD3A/B at approximately 68 kDa. The expected band size for ATAD3A/B is at 72 kDa. https://www.bosterbio.com/catalog/product/view/id/1263932026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263942026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263952026-03-16T05:08:36+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263962026-03-13T05:05:09+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263972026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1263982026-03-16T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08504-laptm4b-primary-antibodies-ihc-testing-1.jpgAnti-LAPTM4B antibodyIHC analysis of LAPTM4B using anti-LAPTM4B antibody (A08504). LAPTM4B was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 200 rabbit anti-LAPTM4B Antibody (A08504) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08504-laptm4b-primary-antibodies-ihc-testing-2.jpgAnti-LAPTM4B antibodyIHC analysis of LAPTM4B using anti-LAPTM4B antibody (A08504). LAPTM4B was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 200 rabbit anti-LAPTM4B Antibody (A08504) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08504-laptm4b-primary-antibodies-ihc-testing-3.jpgAnti-LAPTM4B antibodyIHC analysis of LAPTM4B using anti-LAPTM4B antibody (A08504). LAPTM4B was detected in a paraffin-embedded section of rat ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1: 200 rabbit anti-LAPTM4B Antibody (A08504) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1263992026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264002026-03-16T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08974-1-lias-primary-antibodies-wb-testing-1.jpgAnti-LIAS antibody Western blot analysis of LIAS using anti-LIAS antibody (A08974-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIAS antigen affinity purified polyclonal antibody (A08974-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LIAS at approximately 39 kDa. The expected band size for LIAS is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08974-1-lias-primary-antibodies-ihc-testing-2.jpgAnti-LIAS antibody IHC analysis of LIAS using anti-LIAS antibody (A08974-1). LIAS was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LIAS Antibody (A08974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08974-1-lias-primary-antibodies-ihc-testing-3.jpgAnti-LIAS antibody IHC analysis of LIAS using anti-LIAS antibody (A08974-1). LIAS was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LIAS Antibody (A08974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08974-1-lias-primary-antibodies-ihc-testing-4.jpgAnti-LIAS antibody IHC analysis of LIAS using anti-LIAS antibody (A08974-1). LIAS was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LIAS Antibody (A08974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08974-1-lias-primary-antibodies-ihc-testing-5.jpgAnti-LIAS antibody IHC analysis of LIAS using anti-LIAS antibody (A08974-1). LIAS was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-LIAS Antibody (A08974-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1264012026-03-13T05:05:09+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264022026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08738-2-mepce-primary-antibodies-wb-testing-1.jpgAnti-MEPCE Antibody Picoband®Western blot analysis of MEPCE using anti-MEPCE antibody (A08738-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEPCE antigen affinity purified polyclonal antibody (A08738-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MEPCE at approximately 74 kDa. The expected band size for MEPCE is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08738-2-mepce-primary-antibodies-if-testing-1.jpgAnti-MEPCE Antibody Picoband®IF analysis of MEPCE using anti-MEPCE antibody (A08738-2) and anti-Beta Tubulin antibody (M01857-3). MEPCE was detected in an immunocytochemical section of MCF-7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MEPCE Antibody (A08738-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08738-2-mepce-primary-antibodies-fcm-testing-1.jpgAnti-MEPCE Antibody Picoband®Flow Cytometry analysis of MCF-7 cells using anti-MEPCE antibody (A08738-2). Overlay histogram showing MCF-7 cells stained with A08738-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MEPCE Antibody (A08738-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264032026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264042026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264052026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264062026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264072026-03-16T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-wb-testing-1.jpgAnti-MTCO3 antibody Western blot analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse liver tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTCO3 antigen affinity purified polyclonal antibody (A06912-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MTCO3 at approximately 37 kDa. The expected band size for MTCO3 is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-2.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-3.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-4.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of human glioma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-5.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-6.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-7.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-8.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-9.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of mouse midbrain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-10.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06912-1-mtco3-primary-antibodies-ihc-testing-11.jpgAnti-MTCO3 antibody IHC analysis of MTCO3 using anti-MTCO3 antibody (A06912-1). MTCO3 was detected in a paraffin-embedded section of rat midbrain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 1:100 rabbit anti-MTCO3 Antibody (A06912-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1264082026-03-13T05:05:09+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264092026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264102026-03-13T05:05:09+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264112026-03-13T05:05:09+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264122026-03-16T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11044-1-nsun5-primary-antibodies-wb-testing-1.jpgAnti-NSUN5 antibody Western blot analysis of NSUN5 using anti-NSUN5 antibody (A11044-1). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSUN5 antigen affinity purified polyclonal antibody (A11044-1) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NSUN5 at approximately 50 kDa. The expected band size for NSUN5 is at 47 kDa. https://www.bosterbio.com/catalog/product/view/id/1264132026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264142026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264152026-03-16T05:08:37+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264162026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07034-2-pcgf6-primary-antibodies-wb-testing-1.jpgAnti-PCGF6 Antibody Picoband®Western blot analysis of PCGF6 using anti-PCGF6 antibody (A07034-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCGF6 antigen affinity purified polyclonal antibody (A07034-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PCGF6 at approximately 50 kDa. The expected band size for PCGF6 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07034-2-pcgf6-primary-antibodies-fcm-testing-1.jpgAnti-PCGF6 Antibody Picoband®Flow Cytometry analysis of U251 cells using anti-PCGF6 antibody (A07034-2). Overlay histogram showing U251 cells stained with A07034-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PCGF6 Antibody (A07034-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264172026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10738-3-gimap4-primary-antibodies-wb-testing-1.jpgAnti-GIMAP4 Antibody Picoband® Western blot analysis of GIMAP4 using anti-GIMAP4 antibody (A10738-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: rat spleen tissue lysates, Lane 3: rat thymus tissue lysates, Lane 4: rat lung tissue lysates, Lane 5: mouse spleen tissue lysates, Lane 6: mouse thymus tissue lysates, Lane 7: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GIMAP4 antigen affinity purified polyclonal antibody (Catalog # A10738-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GIMAP4 at approximately 38 kDa. The expected band size for GIMAP4 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10738-3-gimap4-primary-antibodies-ihc-testing-2.jpgAnti-GIMAP4 Antibody Picoband® IHC analysis of GIMAP4 using anti-GIMAP4 antibody (A10738-3). GIMAP4 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIMAP4 Antibody (A10738-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10738-3-gimap4-primary-antibodies-ihc-testing-3.jpgAnti-GIMAP4 Antibody Picoband® IHC analysis of GIMAP4 using anti-GIMAP4 antibody (A10738-3). GIMAP4 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIMAP4 Antibody (A10738-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10738-3-gimap4-primary-antibodies-ihc-testing-4.jpgAnti-GIMAP4 Antibody Picoband® IHC analysis of GIMAP4 using anti-GIMAP4 antibody (A10738-3). GIMAP4 was detected in a paraffin-embedded section of rat thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIMAP4 Antibody (A10738-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10738-3-gimap4-primary-antibodies-ihc-testing-5.jpgAnti-GIMAP4 Antibody Picoband® IHC analysis of GIMAP4 using anti-GIMAP4 antibody (A10738-3). GIMAP4 was detected in a paraffin-embedded section of rat thymus tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIMAP4 Antibody (A10738-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10738-3-gimap4-primary-antibodies-fcm-testing-6.jpgAnti-GIMAP4 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-GIMAP4 antibody (A10738-3). Overlay histogram showing JK cells stained with A10738-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GIMAP4 Antibody (A10738-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264192026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03531-nfia-primary-antibodies-wb-testing-1.jpgAnti-NFIA Antibody Picoband® Western blot analysis of NFIA using anti-NFIA antibody (A03531). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse L929 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NFIA antigen affinity purified polyclonal antibody (Catalog # A03531) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NFIA at approximately 70 kDa. The expected band size for NFIA is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03531-nfia-primary-antibodies-fcm-testing-2.jpgAnti-NFIA Antibody Picoband® Flow Cytometry analysis of JK cells using anti-NFIA antibody (A03531). Overlay histogram showing JK cells stained with A03531 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NFIA Antibody (A03531, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264222026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08857-1-itm2c-primary-antibodies-wb-testing-1.jpgAnti-ITM2C Antibody Picoband® Western blot analysis of ITM2C using anti-ITM2C antibody (A08857-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITM2C antigen affinity purified polyclonal antibody (Catalog # A08857-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITM2C at approximately 35 kDa. The expected band size for ITM2C is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08857-1-itm2c-primary-antibodies-fcm-testing-2.jpgAnti-ITM2C Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-ITM2C antibody (A08857-1). Overlay histogram showing CACO-2 cells stained with A08857-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ITM2C Antibody (A08857-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08857-1-itm2c-primary-antibodies-fcm-testing-3.jpgAnti-ITM2C Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-ITM2C antibody (A08857-1). Overlay histogram showing PC-3 cells stained with A08857-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ITM2C Antibody (A08857-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264232026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-wb-testing-1.jpgAnti-HADHA Antibody Picoband® Western blot analysis of HADHA using anti-HADHA antibody (A03666-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HELA whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HADHA antigen affinity purified polyclonal antibody (Catalog # A03666-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. A specific band was detected for HADHA at approximately 79 kDa. The expected band size for HADHA is at 83 kDa. Lane 1: human 293T whole cell lysates, Lane 2: human HELA whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HADHA antigen affinity purified polyclonal antibody (Catalog # A03666-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HADHA at approximately 79 kDa. The expected band size for HADHA is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-wb-testing-2.jpgAnti-HADHA Antibody Picoband® Western blot analysis of HADHA using anti-HADHA antibody (A03666-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat kidney tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HADHA antigen affinity purified polyclonal antibody (Catalog # A03666-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HADHA at approximately 79 kDa. The expected band size for HADHA is at 83 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-3.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-4.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-5.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-6.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human colon adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-7.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-8.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-9.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-10.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-11.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-12.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-13.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-14.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-15.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-ihc-testing-16.jpgAnti-HADHA Antibody Picoband® IHC analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human thyroid papillary carcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-if-testing-17.jpgAnti-HADHA Antibody Picoband® IF analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in an immunocytochemical section of MG63 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-if-testing-1.jpgAnti-HADHA Antibody Picoband®IF analysis of HADHA using anti-HADHA antibody (A03666-2). HADHA was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-HADHA Antibody (A03666-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03666-2-hadha-primary-antibodies-fcm-testing-18.jpgAnti-HADHA Antibody Picoband® Flow Cytometry analysis of JK cells using anti-HADHA antibody (A03666-2). Overlay histogram showing JK cells stained with A03666-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HADHA Antibody (A03666-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264242026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09943-3-gins2-primary-antibodies-wb-testing-1.jpgAnti-PSF2/GINS2 Antibody Picoband® Western blot analysis of PSF2/GINS2 using anti-PSF2/GINS2 antibody (A09943-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PSF2/GINS2 antigen affinity purified polyclonal antibody (Catalog # A09943-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PSF2/GINS2 at approximately 21 kDa. The expected band size for PSF2/GINS2 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09943-3-gins2-primary-antibodies-ip-testing-1.jpgAnti-PSF2/GINS2 Antibody Picoband®Immunoprecipitating (IP) PSF2/GINS2 in 293T whole cell lysate. Western blot analysis of PSF2/GINS2 using anti-PSF2/GINS2 antibody (A09943-3); Lane 1: 293T whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-PSF2/GINS2 antibody in 293T whole cell lysate; Lane 3: anti-PSF2/GINS2 antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PSF2/GINS2 antigen affinity purified polyclonal antibody (A09943-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PSF2/GINS2 at approximately 21 kDa. The expected band size for PSF2/GINS2 is at 21 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09943-3-gins2-primary-antibodies-fcm-testing-2.jpgAnti-PSF2/GINS2 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-PSF2/GINS2 antibody (A09943-3). Overlay histogram showing A549 cells stained with A09943-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSF2/GINS2 Antibody (A09943-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09943-3-gins2-primary-antibodies-fcm-testing-3.jpgAnti-PSF2/GINS2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-PSF2/GINS2 antibody (A09943-3). Overlay histogram showing JK cells stained with A09943-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PSF2/GINS2 Antibody (A09943-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264252026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10458-1-gins3-primary-antibodies-wb-testing-1.jpgAnti-GINS3 Antibody Picoband® Western blot analysis of GINS3 using anti-GINS3 antibody (A10458-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GINS3 antigen affinity purified polyclonal antibody (Catalog # A10458-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GINS3 at approximately 25 kDa. The expected band size for GINS3 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10458-1-gins3-primary-antibodies-if-testing-2.jpgAnti-GINS3 Antibody Picoband® IF analysis of GINS3 using anti-GINS3 antibody (A10458-1). GINS3 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GINS3 Antibody (A10458-1) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10458-1-gins3-primary-antibodies-fcm-testing-3.jpgAnti-GINS3 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-GINS3 antibody (A10458-1). Overlay histogram showing Caco-2 cells stained with A10458-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GINS3 Antibody (A10458-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264262026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10548-1-gins4-primary-antibodies-wb-testing-1.jpgAnti-SLD5/GINS4 Antibody Picoband® Western blot analysis of SLD5/GINS4 using anti-SLD5/GINS4 antibody (A10548-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A375 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SLD5/GINS4 antigen affinity purified polyclonal antibody (Catalog # A10548-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SLD5/GINS4 at approximately 28 kDa. The expected band size for SLD5/GINS4 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10548-1-gins4-primary-antibodies-ihc-testing-2.jpgAnti-SLD5/GINS4 Antibody Picoband® IHC analysis of SLD5/GINS4 using anti-SLD5/GINS4 antibody (A10548-1). SLD5/GINS4 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLD5/GINS4 Antibody (A10548-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10548-1-gins4-primary-antibodies-ihc-testing-3.jpgAnti-SLD5/GINS4 Antibody Picoband® IHC analysis of SLD5/GINS4 using anti-SLD5/GINS4 antibody (A10548-1). SLD5/GINS4 was detected in a paraffin-embedded section of human melanoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SLD5/GINS4 Antibody (A10548-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10548-1-gins4-primary-antibodies-fcm-testing-4.jpgAnti-SLD5/GINS4 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-SLD5/GINS4 antibody (A10548-1). Overlay histogram showing A549 cells stained with A10548-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SLD5/GINS4 Antibody (A10548-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264272026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-wb-testing-1.jpgAnti-GIPC1 Antibody Picoband® Western blot analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: rat skeletal muscle tissue lysates, Lane 4: rat brain tissue lysates, Lane 5: rat NRK whole cell lysates, Lane 6: mouse skeletal muscle tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GIPC1 antigen affinity purified polyclonal antibody (Catalog # A04969-4) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GIPC1 at approximately 40 kDa. The expected band size for GIPC1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-ihc-testing-2.jpgAnti-GIPC1 Antibody Picoband® IHC analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). GIPC1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIPC1 Antibody (A04969-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-ihc-testing-3.jpgAnti-GIPC1 Antibody Picoband® IHC analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). GIPC1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIPC1 Antibody (A04969-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-ihc-testing-4.jpgAnti-GIPC1 Antibody Picoband® IHC analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). GIPC1 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIPC1 Antibody (A04969-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-ihc-testing-5.jpgAnti-GIPC1 Antibody Picoband® IHC analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). GIPC1 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIPC1 Antibody (A04969-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-ihc-testing-6.jpgAnti-GIPC1 Antibody Picoband® IHC analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). GIPC1 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIPC1 Antibody (A04969-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-ihc-testing-7.jpgAnti-GIPC1 Antibody Picoband® IHC analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). GIPC1 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GIPC1 Antibody (A04969-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-if-testing-8.jpgAnti-GIPC1 Antibody Picoband® IF analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). GIPC1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GIPC1 Antibody (A04969-4) overnight at 4°C. DyLight®594 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. The tissue section was developed using Phalloidin-iFluor 488 Conjugated. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-ip-testing-1.jpgAnti-GIPC1 Antibody Picoband®Immunoprecipitating GIPC1 in A431 whole cell lysate. Western blot analysis of GIPC1 using anti-GIPC1 antibody (A04969-4). Lane 1: A431 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-GIPC1 antibody in A431 whole cell lysate, Lane 3: anti-GIPC1 antibody (2μg) + A431 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GIPC1 antigen affinity purified polyclonal antibody (A04969-4) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for GIPC1 at approximately 40 kDa. The expected band size for GIPC1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04969-4-gipc1-primary-antibodies-fcm-testing-9.jpgAnti-GIPC1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GIPC1 antibody (A04969-4). Overlay histogram showing HepG2 cells stained with A04969-4 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GIPC1 Antibody (A04969-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264282026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12674-2-gipc3-primary-antibodies-wb-testing-1.jpgAnti-GIPC3 Antibody Picoband® Western blot analysis of GIPC3 using anti-GIPC3 antibody (A12674-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human K562 whole cell lysates, Lane 5: rat H9C2(2-1) whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GIPC3 antigen affinity purified polyclonal antibody (Catalog # A12674-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GIPC3 at approximately 40 kDa. The expected band size for GIPC3 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12674-2-gipc3-primary-antibodies-if-testing-2_1.jpgAnti-GIPC3 Antibody Picoband® IF analysis of GIPC3 using anti-GIPC3 antibody (A12674-2) and anti-Beta Tubulin antibody (M01857-3). GIPC3 was detected in immunocytochemical section of SiHa cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GIPC3 Antibody (A12674-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12674-2-gipc3-primary-antibodies-fcm-testing-3.jpgAnti-GIPC3 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-GIPC3 antibody (A12674-2). Overlay histogram showing K562 cells stained with A12674-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GIPC3 Antibody (A12674-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264292026-03-17T05:16:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05766-1-nfkbib-primary-antibodies-wb-testing-1.jpgAnti-IkB Beta/NFKBIB Antibody Picoband® Western blot analysis of IkB Beta/NFKBIB using anti-IkB Beta/NFKBIB antibody (A05766-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IkB Beta/NFKBIB antigen affinity purified polyclonal antibody (Catalog # A05766-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IkB Beta/NFKBIB at approximately 45 kDa. The expected band size for IkB Beta/NFKBIB is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05766-1-nfkbib-primary-antibodies-fcm-testing-2.jpgAnti-IkB Beta/NFKBIB Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-IkB Beta/NFKBIB antibody (A05766-1). Overlay histogram showing PC-3 cells stained with A05766-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IkB Beta/NFKBIB Antibody (A05766-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264302026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00529-3-cd49-primary-antibodies-wb-testing-1.jpgAnti-CD69 Antibody Picoband® Western blot analysis of CD69 using anti-CD69 antibody (A00529-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CD69 antigen affinity purified polyclonal antibody (Catalog # A00529-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CD69 at approximately 32 kDa. The expected band size for CD69 is at 23 kDa. https://www.bosterbio.com/catalog/product/view/id/1264312026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15997-gk5-primary-antibodies-wb-testing-1.jpgAnti-GK5 Antibody Picoband® Western blot analysis of GK5 using anti-GK5 antibody (A15997). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GK5 antigen affinity purified polyclonal antibody (Catalog # A15997) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GK5 at approximately 59 kDa. The expected band size for GK5 is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15997-gk5-primary-antibodies-fcm-testing-2.jpgAnti-GK5 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-GK5 antibody (A15997). Overlay histogram showing JK cells stained with A15997 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GK5 Antibody (A15997, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264322026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14397-1-gkap1-primary-antibodies-wb-testing-1.jpgAnti-GKAP1 Antibody Picoband® Western blot analysis of GKAP1 using anti-GKAP1 antibody (A14397-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GKAP1 antigen affinity purified polyclonal antibody (Catalog # A14397-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GKAP1 at approximately 40-42 kDa. The expected band size for GKAP1 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14397-1-gkap1-primary-antibodies-fcm-testing-2.jpgAnti-GKAP1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-GKAP1 antibody (A14397-1). Overlay histogram showing SH-SY5Y cells stained with A14397-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GKAP1 Antibody (A14397-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264342026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-wb-testing-1.jpgAnti-SOS1 Antibody Picoband® Western blot analysis of SOS1 using anti-SOS1 antibody (A00837-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SOS1 antigen affinity purified polyclonal antibody (Catalog # A00837-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SOS1 at approximately 170 kDa. The expected band size for SOS1 is at 152 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-ihc-testing-2.jpgAnti-SOS1 Antibody Picoband® IHC analysis of SOS1 using anti-SOS1 antibody (A00837-1). SOS1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOS1 Antibody (A00837-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-ihc-testing-3.jpgAnti-SOS1 Antibody Picoband® IHC analysis of SOS1 using anti-SOS1 antibody (A00837-1). SOS1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOS1 Antibody (A00837-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-ihc-testing-4.jpgAnti-SOS1 Antibody Picoband® IHC analysis of SOS1 using anti-SOS1 antibody (A00837-1). SOS1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOS1 Antibody (A00837-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-ihc-testing-5.jpgAnti-SOS1 Antibody Picoband® IHC analysis of SOS1 using anti-SOS1 antibody (A00837-1). SOS1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOS1 Antibody (A00837-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-ihc-testing-6.jpgAnti-SOS1 Antibody Picoband® IHC analysis of SOS1 using anti-SOS1 antibody (A00837-1). SOS1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOS1 Antibody (A00837-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-ihc-testing-7.jpgAnti-SOS1 Antibody Picoband® IHC analysis of SOS1 using anti-SOS1 antibody (A00837-1). SOS1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SOS1 Antibody (A00837-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-fcm-testing-8.jpgAnti-SOS1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-SOS1 antibody (A00837-1). Overlay histogram showing K562 cells stained with A00837-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SOS1 Antibody (A00837-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00837-1-sos1-primary-antibodies-fcm-testing-9.jpgAnti-SOS1 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-SOS1 antibody (A00837-1). Overlay histogram showing U87 cells stained with A00837-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-SOS1 Antibody (A00837-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264432026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14243-tmem201-primary-antibodies-wb-testing-1.jpgAnti-TMEM201 Antibody Picoband® Western blot analysis of TMEM201 using anti-TMEM201 antibody (A14243). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TMEM201 antigen affinity purified polyclonal antibody (Catalog # A14243) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TMEM201 at approximately 85 kDa. The expected band size for TMEM201 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14243-tmem201-primary-antibodies-fcm-testing-2.jpgAnti-TMEM201 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-TMEM201 antibody (A14243). Overlay histogram showing Caco-2 cells stained with A14243 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TMEM201 Antibody (A14243, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264442026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04143-1-tom1-primary-antibodies-wb-testing-1.jpgAnti-TOM1 Antibody Picoband® Western blot analysis of TOM1 using anti-TOM1 antibody (A04143-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TOM1 antigen affinity purified polyclonal antibody (Catalog # A04143-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TOM1 at approximately 54 kDa. The expected band size for TOM1 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04143-1-tom1-primary-antibodies-ihc-testing-2.jpgAnti-TOM1 Antibody Picoband® IHC analysis of TOM1 using anti-TOM1 antibody (A04143-1). TOM1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TOM1 Antibody (A04143-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04143-1-tom1-primary-antibodies-ihc-testing-3.jpgAnti-TOM1 Antibody Picoband® IHC analysis of TOM1 using anti-TOM1 antibody (A04143-1). TOM1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TOM1 Antibody (A04143-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04143-1-tom1-primary-antibodies-if-testing-4.jpgAnti-TOM1 Antibody Picoband® IF analysis of TOM1 using anti-TOM1 antibody (A04143-1). TOM1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TOM1 Antibody (A04143-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1142) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04143-1-tom1-primary-antibodies-fcm-testing-5.jpgAnti-TOM1 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-TOM1 antibody (A04143-1). Overlay histogram showing Hela cells stained with A04143-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TOM1 Antibody (A04143-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04143-1-tom1-primary-antibodies-ip-testing-6.jpgAnti-TOM1 Antibody Picoband® Immunoprecipitating TOM1 in HepG2 whole cell lysate. Western blot analysis of TOM1 using anti-TOM1 antibody (A04143-1). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-TOM1 antibody in HepG2 whole cell lysate, Lane 3: anti-TOM1 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-TOM1 antigen affinity purified polyclonal antibody (A04143-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Light chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for TOM1 at approximately 54 kDa. The expected band size for TOM1 is at 54 kDa. https://www.bosterbio.com/catalog/product/view/id/1264462026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-wb-testing-1.jpgAnti-SBK1 Antibody Picoband® Western blot analysis of SBK1 using anti-SBK1 antibody (A17120-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SBK1 antigen affinity purified polyclonal antibody (Catalog # A17120-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SBK1 at approximately 43 kDa. The expected band size for SBK1 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-ihc-testing-2.jpgAnti-SBK1 Antibody Picoband® IHC analysis of SBK1 using anti-SBK1 antibody (A17120-1). SBK1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SBK1 Antibody (A17120-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-ihc-testing-3.jpgAnti-SBK1 Antibody Picoband® IHC analysis of SBK1 using anti-SBK1 antibody (A17120-1). SBK1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SBK1 Antibody (A17120-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-ihc-testing-4.jpgAnti-SBK1 Antibody Picoband® IHC analysis of SBK1 using anti-SBK1 antibody (A17120-1). SBK1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SBK1 Antibody (A17120-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-ihc-testing-5.jpgAnti-SBK1 Antibody Picoband® IHC analysis of SBK1 using anti-SBK1 antibody (A17120-1). SBK1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SBK1 Antibody (A17120-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-ihc-testing-6.jpgAnti-SBK1 Antibody Picoband® IHC analysis of SBK1 using anti-SBK1 antibody (A17120-1). SBK1 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SBK1 Antibody (A17120-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-ihc-testing-7.jpgAnti-SBK1 Antibody Picoband® IHC analysis of SBK1 using anti-SBK1 antibody (A17120-1). SBK1 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SBK1 Antibody (A17120-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-fcm-testing-8.jpgAnti-SBK1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-SBK1 antibody (A17120-1). Overlay histogram showing SH-SY5Y cells stained with A17120-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SBK1 Antibody (A17120-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17120-1-sbk1-primary-antibodies-ip-testing-9.jpgAnti-SBK1 Antibody Picoband® Immunoprecipitating SBK1 in MCF-7 whole cell lysate. Western blot analysis of SBK1 using anti-SBK1 antibody (A17120-1); Lane 1: MCF-7 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-SBK1 antibody in MCF-7 whole cell lysate; Lane 3: anti-SBK1 antibody (2μg) + MCF-7 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SBK1 antigen affinity purified polyclonal antibody (A17120-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for SBK1 at approximately 46 kDa. The expected band size for SBK1 is at 46 kDa. https://www.bosterbio.com/catalog/product/view/id/1264482026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06489-glrx3-primary-antibodies-wb-testing-1.jpgAnti-GLRX3 Antibody Picoband® Western blot analysis of GLRX3 using anti-GLRX3 antibody (A06489). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLRX3 antigen affinity purified polyclonal antibody (Catalog # A06489) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLRX3 at approximately 40 kDa. The expected band size for GLRX3 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06489-glrx3-primary-antibodies-fcm-testing-2.jpgAnti-GLRX3 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-GLRX3 antibody (A06489). Overlay histogram showing JK cells stained with A06489 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLRX3 Antibody (A06489, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264492026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09506-1-glyat-primary-antibodies-wb-testing-1.jpgAnti-GLYAT Antibody Picoband® Western blot analysis of GLYAT using anti-GLYAT antibody (A09506-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human hepatocellular carcinoma tumor tissue (HCCT) lysates, Lane 2: rat kidney tissue lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse kidney tissue lysates, Lane 5: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLYAT antigen affinity purified polyclonal antibody (Catalog # A09506-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLYAT at approximately 34 kDa. The expected band size for GLYAT is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09506-1-glyat-primary-antibodies-fcm-testing-2.jpgAnti-GLYAT Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-GLYAT antibody (A09506-1). Overlay histogram showing RT4 cells stained with A09506-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLYAT Antibody (A09506-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264502026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00078-2-nrf2-primary-antibodies-wb-testing-1.jpgAnti-NRF2/NFE2L2 Antibody Picoband® Western blot analysis of NRF2/NFE2L2 using anti-NRF2/NFE2L2 antibody (A00078-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: human U20S(+MG132) whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NRF2/NFE2L2 antigen affinity purified polyclonal antibody (Catalog # A00078-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NRF2/NFE2L2 at approximately 100-110 kDa. The expected band size for NRF2/NFE2L2 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00078-2-nrf2-primary-antibodies-fcm-testing-2.jpgAnti-NRF2/NFE2L2 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-NRF2/NFE2L2 antibody (A00078-2). Overlay histogram showing RT4 cells stained with A00078-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NRF2/NFE2L2 Antibody (A00078-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264512026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07334-2-sec61b-primary-antibodies-wb-testing-1.jpgAnti-SEC61B Antibody Picoband® Western blot analysis of SEC61B using anti-SEC61B antibody (A07334-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse C2C12 whole cell lysates, Lane 7: mouse RAW264.7 whole cell lysates, Lane 8: mouse 3T3-L1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SEC61B antigen affinity purified polyclonal antibody (Catalog # A07334-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SEC61B at approximately 15 kDa. The expected band size for SEC61B is at 10 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07334-2-sec61b-primary-antibodies-fcm-testing-2.jpgAnti-SEC61B Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-SEC61B antibody (A07334-2). Overlay histogram showing PC-3 cells stained with A07334-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SEC61B Antibody (A07334-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264522026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04376-1-slc17a6-primary-antibodies-wb-testing-1.jpgAnti-VGLUT2/SLC17A6 Antibody Picoband® Western blot analysis of VGLUT2/SLC17A6 using anti-VGLUT2/SLC17A6 antibody (A04376-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human U-87MG whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-VGLUT2/SLC17A6 antigen affinity purified polyclonal antibody (Catalog # A04376-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for VGLUT2/SLC17A6 at approximately 64 kDa. The expected band size for VGLUT2/SLC17A6 is at 64 kDa. https://www.bosterbio.com/catalog/product/view/id/1264532026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07845-1-itpkc-primary-antibodies-wb-testing-1.jpgAnti-ITPKC Antibody Picoband® Western blot analysis of ITPKC using anti-ITPKC antibody (A07845-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ITPKC antigen affinity purified polyclonal antibody (Catalog # A07845-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ITPKC at approximately 100 kDa. The expected band size for ITPKC is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07845-1-itpkc-primary-antibodies-fcm-testing-2.jpgAnti-ITPKC Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-ITPKC antibody (A07845-1). Overlay histogram showing Caco-2 cells stained with A07845-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ITPKC Antibody (A07845-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264542026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-wb-testing-1.jpgAnti-DIS3 Antibody Picoband® Western blot analysis of DIS3 using anti-DIS3 antibody (A01736-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DIS3 antigen affinity purified polyclonal antibody (Catalog # A01736-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DIS3 at approximately 109 kDa. The expected band size for DIS3 is at 109 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-2.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-3.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-4.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-5.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-6.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-7.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-8.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-ihc-testing-9.jpgAnti-DIS3 Antibody Picoband® IHC analysis of DIS3 using anti-DIS3 antibody (A01736-2). DIS3 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DIS3 Antibody (A01736-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-if-testing-10.jpgAnti-DIS3 Antibody Picoband® IF analysis of DIS3 using anti-DIS3 antibody (A01736-2) and anti-Beta Tubulin antibody (M01857-3). DIS3 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DIS3 Antibody (A01736-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01736-2-dis3-primary-antibodies-fcm-testing-11.jpgAnti-DIS3 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-DIS3 antibody (A01736-2). Overlay histogram showing MCF-7 cells stained with A01736-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DIS3 Antibody (A01736-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264552026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07510-1-glg1-primary-antibodies-wb-testing-1.jpgAnti-GLG1 Antibody Picoband® Western blot analysis of GLG1 using anti-GLG1 antibody (A07510-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLG1 antigen affinity purified polyclonal antibody (Catalog # A07510-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLG1 at approximately 150 kDa. The expected band size for GLG1 is at 135 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07510-1-glg1-primary-antibodies-ihc-testing-2.jpgAnti-GLG1 Antibody Picoband® IHC analysis of GLG1 using anti-GLG1 antibody (A07510-1). GLG1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLG1 Antibody (A07510-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07510-1-glg1-primary-antibodies-ihc-testing-3.jpgAnti-GLG1 Antibody Picoband® IHC analysis of GLG1 using anti-GLG1 antibody (A07510-1). GLG1 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLG1 Antibody (A07510-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07510-1-glg1-primary-antibodies-ihc-testing-4.jpgAnti-GLG1 Antibody Picoband® IHC analysis of GLG1 using anti-GLG1 antibody (A07510-1). GLG1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLG1 Antibody (A07510-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07510-1-glg1-primary-antibodies-ihc-testing-5.jpgAnti-GLG1 Antibody Picoband® IHC analysis of GLG1 using anti-GLG1 antibody (A07510-1). GLG1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLG1 Antibody (A07510-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07510-1-glg1-primary-antibodies-fcm-testing-6..jpgAnti-GLG1 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-GLG1 antibody (A07510-1). Overlay histogram showing SiHa cells stained with A07510-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLG1 Antibody (A07510-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264562026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04859-1-aph1a-primary-antibodies-wb-testing-1.jpgAnti-APH1A Antibody Picoband® Western blot analysis of APH1A using anti-APH1A antibody (A04859-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APH1A antigen affinity purified polyclonal antibody (Catalog # A04859-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for APH1A at approximately 29 kDa. The expected band size for APH1A is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04859-1-aph1a-primary-antibodies-ihc-testing-2.jpgAnti-APH1A Antibody Picoband® IHC analysis of APH1A using anti-APH1A antibody (A04859-1). APH1A was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APH1A Antibody (A04859-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04859-1-aph1a-primary-antibodies-ihc-testing-3.jpgAnti-APH1A Antibody Picoband® IHC analysis of APH1A using anti-APH1A antibody (A04859-1). APH1A was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APH1A Antibody (A04859-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04859-1-aph1a-primary-antibodies-ihc-testing-4.jpgAnti-APH1A Antibody Picoband® IHC analysis of APH1A using anti-APH1A antibody (A04859-1). APH1A was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APH1A Antibody (A04859-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04859-1-aph1a-primary-antibodies-if-testing-1.jpgAnti-APH1A Antibody Picoband®IF analysis of APH1A using anti-APH1A antibody (A04859-13). APH1A was detected in a paraffin-embedded section of mouse colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-APH1A Antibody (A04859-1) overnight at 4°C. DyLight®550 Conjugated Donkey Anti-Rabbit IgG (BA1144) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04859-1-aph1a-primary-antibodies-if-testing-2.jpgAnti-APH1A Antibody Picoband®IF analysis of APH1A using anti-APH1A antibody (A04859-13). APH1A was detected in a paraffin-embedded section of rat colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-APH1A Antibody (A04859-1) overnight at 4°C. DyLight®550 Conjugated Donkey Anti-Rabbit IgG (BA1144) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04859-1-aph1a-primary-antibodies-fcm-testing-5.jpgAnti-APH1A Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-APH1A antibody (A04859-1). Overlay histogram showing MCF-7 cells stained with A04859-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-APH1A Antibody (A04859-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264572026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13834-1-hifnt-primary-antibodies-wb-testing-1.jpgAnti-H1-7 Antibody Picoband® Western blot analysis of H1-7 using anti-H1-7 antibody (A13834-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat lung tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse lung tissue lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse testis tissue lysates, After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-H1-7 antigen affinity purified polyclonal antibody (Catalog # A13834-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for H1-7 at approximately 28 kDa. The expected band size for H1-7 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13834-1-hifnt-primary-antibodies-fcm-testing-2.jpgAnti-H1-7 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-H1-7 antibody (A13834-1). Overlay histogram showing JK cells stained with A13834-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-H1-7 Antibody (A13834-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264582026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-glipr2-primary-antibodies-wb-testing-1.jpgAnti-GLIPR2 Antibody Picoband® Western blot analysis of GLIPR2 using anti-GLIPR2 antibody (A10232-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 8: mouse brain tissue lysates, Lane 9: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLIPR2 antigen affinity purified polyclonal antibody (Catalog # A10232-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLIPR2 at approximately 17 kDa. The expected band size for GLIPR2 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-41598_2025_98754_fig7_html.pngAnti-GLIPR2 Antibody Picoband®Characterized genes and immune cells correlation analysis between sham and SAH 1d samples. Lollipop charts of the correlation of LCN2 ( A ), A2M ( B ), GLIPR2 ( C ), GPNMB ( D ), GFAP ( E ), respectively, with 22 immune cell types. Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41598-025-98754-x'>40274967</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-41598_2025_98754_fig10_html.pngAnti-GLIPR2 Antibody Picoband®A2M and GLIPR2 are highly expressed after SAH. ( A , C ) Western blot images and quantitative analyses of A2M and GLIPR2 in rat cortical tissues. ( B ) Western blot images of A2M and GLIPR2 in the cerebrospinal fluid of patients. (* p < 0.05, ** p < 0.01, *** p < 0.001) Index in PubMed under a CC BY license. PMID: <a href='https://www.nature.com/articles/s41598-025-98754-x'>40274967</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-glipr2-primary-antibodies-ihc-testing-2.jpgAnti-GLIPR2 Antibody Picoband® IHC analysis of GLIPR2 using anti-GLIPR2 antibody (A10232-1). GLIPR2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLIPR2 Antibody (A10232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-glipr2-primary-antibodies-ihc-testing-3.jpgAnti-GLIPR2 Antibody Picoband® IHC analysis of GLIPR2 using anti-GLIPR2 antibody (A10232-1). GLIPR2 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLIPR2 Antibody (A10232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-glipr2-primary-antibodies-ihc-testing-4.jpgAnti-GLIPR2 Antibody Picoband® IHC analysis of GLIPR2 using anti-GLIPR2 antibody (A10232-1). GLIPR2 was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLIPR2 Antibody (A10232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-glipr2-primary-antibodies-ihc-testing-5.jpgAnti-GLIPR2 Antibody Picoband® IHC analysis of GLIPR2 using anti-GLIPR2 antibody (A10232-1). GLIPR2 was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLIPR2 Antibody (A10232-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-glipr2-primary-antibodies-fcm-testing-6.jpgAnti-GLIPR2 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-GLIPR2 antibody (A10232-1). Overlay histogram showing THP-1 cells stained with A10232-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLIPR2 Antibody (A10232-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10232-1-glipr2-primary-antibodies-ip-testing-7.jpgAnti-GLIPR2 Antibody Picoband® Immunoprecipitating GLIPR2 in U251 whole cell lysate. Western blot analysis of GLIPR2 using anti-GLIPR2 antibody (A10232-1). Lane 1: U251 whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-GLIPR2 antibody in U251 whole cell lysate. Lane 3: anti-GLIPR2 antibody (2μg) + U251 whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GLIPR2 antigen affinity purified polyclonal antibody (A10232-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for GLIPR2 at approximately 17 kDa. The expected band size for GLIPR2 is at 17 kDa. https://www.bosterbio.com/catalog/product/view/id/1264592026-03-17T05:16:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07319-1-glmn-primary-antibodies-wb-testing-1.jpgAnti-GLMN Antibody Picoband® Western blot analysis of GLMN using anti-GLMN antibody (A07319-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLMN antigen affinity purified polyclonal antibody (Catalog # A07319-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLMN at approximately 68 kDa. The expected band size for GLMN is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07319-1-glmn-primary-antibodies-fcm-testing-2.jpgAnti-GLMN Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-GLMN antibody (A07319-1). Overlay histogram showing 293T cells stained with A07319-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLMN Antibody (A07319-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264612026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00868-1-anxa2-primary-antibodies-wb-testing-1.jpgAnti-Annexin A2/ANXA2 Antibody Picoband® Western blot analysis of Annexin A2/ANXA2 using anti-Annexin A2/ANXA2 antibody (A00868-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human placenta tissue lysates, Lane 5: rat kidney tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse kidney tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Annexin A2/ANXA2 antigen affinity purified polyclonal antibody (Catalog # A00868-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Annexin A2/ANXA2 at approximately 36 kDa. The expected band size for Annexin A2/ANXA2 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00868-1-anxa2-primary-antibodies-fcm-testing-2.jpgAnti-Annexin A2/ANXA2 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-Annexin A2/ANXA2 antibody (A00868-1). Overlay histogram showing Hela cells stained with A00868-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Annexin A2/ANXA2 Antibody (A00868-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264632026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05402-4-hspa6-primary-antibodies-wb-testing-1.jpgAnti-HSPA6 Antibody Picoband® Western blot analysis of HSPA6 using anti-HSPA6 antibody (A05402-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA6 antigen affinity purified polyclonal antibody (Catalog # A05402-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSPA6 at approximately 71 kDa. The expected band size for HSPA6 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05402-4-hspa6-primary-antibodies-fcm-testing-2.jpgAnti-HSPA6 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-HSPA6 antibody (A05402-4). Overlay histogram showing PC-3 cells stained with A05402-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSPA6 Antibody (A05402-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05402-4-hspa6-primary-antibodies-wb-testing-3.jpgAnti-HSPA6 Antibody Picoband® Western blot analysis of HSPA6 using anti-HSPA6 antibody (A05402-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA6 antigen affinity purified polyclonal antibody (A05402-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for HSPA6 at approximately 71 kDa. The expected band size for HSPA6 is at 71 kDa. https://www.bosterbio.com/catalog/product/view/id/1264642026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-wb-testing-1.jpgAnti-FAM40B/STRIP2 Antibody Picoband® Western blot analysis of FAM40B/STRIP2 using anti-FAM40B/STRIP2 antibody (A12139). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human SiHa whole cell lysates, Lane 5: rat testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAM40B/STRIP2 antigen affinity purified polyclonal antibody (Catalog # A12139) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FAM40B/STRIP2 at approximately 100 kDa. The expected band size for FAM40B/STRIP2 is at 95 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-ihc-testing-2.jpgAnti-FAM40B/STRIP2 Antibody Picoband® IHC analysis of FAM40B/STRIP2 using anti-FAM40B/STRIP2 antibody (A12139). FAM40B/STRIP2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM40B/STRIP2 Antibody (A12139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-ihc-testing-3.jpgAnti-FAM40B/STRIP2 Antibody Picoband® IHC analysis of FAM40B/STRIP2 using anti-FAM40B/STRIP2 antibody (A12139). FAM40B/STRIP2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM40B/STRIP2 Antibody (A12139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-ihc-testing-4.jpgAnti-FAM40B/STRIP2 Antibody Picoband® IHC analysis of FAM40B/STRIP2 using anti-FAM40B/STRIP2 antibody (A12139). FAM40B/STRIP2 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM40B/STRIP2 Antibody (A12139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-ihc-testing-5.jpgAnti-FAM40B/STRIP2 Antibody Picoband® IHC analysis of FAM40B/STRIP2 using anti-FAM40B/STRIP2 antibody (A12139). FAM40B/STRIP2 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM40B/STRIP2 Antibody (A12139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-ihc-testing-6.jpgAnti-FAM40B/STRIP2 Antibody Picoband® IHC analysis of FAM40B/STRIP2 using anti-FAM40B/STRIP2 antibody (A12139). FAM40B/STRIP2 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM40B/STRIP2 Antibody (A12139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-ihc-testing-7.jpgAnti-FAM40B/STRIP2 Antibody Picoband® IHC analysis of FAM40B/STRIP2 using anti-FAM40B/STRIP2 antibody (A12139). FAM40B/STRIP2 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FAM40B/STRIP2 Antibody (A12139) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12139-strip2-primary-antibodies-fcm-testing-8.jpgAnti-FAM40B/STRIP2 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-FAM40B/STRIP2 antibody (A12139). Overlay histogram showing U87 cells stained with A12139 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FAM40B/STRIP2 Antibody (A12139, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264652026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12454-stx10-primary-antibodies-wb-testing-1.jpgAnti-Syntaxin 10/STX10 Antibody Picoband® Western blot analysis of Syntaxin 10/STX10 using anti-Syntaxin 10/STX10 antibody (A12454). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Syntaxin 10/STX10 antigen affinity purified polyclonal antibody (Catalog # A12454) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Syntaxin 10/STX10 at approximately 32 kDa. The expected band size for Syntaxin 10/STX10 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12454-stx10-primary-antibodies-fcm-testing-2.jpgAnti-Syntaxin 10/STX10 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-Syntaxin 10/STX10 antibody (A12454). Overlay histogram showing JK cells stained with A12454 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Syntaxin 10/STX10 Antibody (A12454, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12454-stx10-primary-antibodies-if-testing-3.jpgAnti-Syntaxin 10/STX10 Antibody Picoband® IF analysis of Syntaxin 10/STX10 using anti-Syntaxin 10/STX10 antibody (A12454). Syntaxin 10/STX10 was detected in immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5μg/mL rabbit anti-Syntaxin 10/STX10 Antibody (A12454) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:100 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1264672026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06705-2-rad51ap1-primary-antibodies-wb-testing-1.jpgAnti-RAD51AP1 Antibody Picoband® Western blot analysis of RAD51AP1 using anti-RAD51AP1 antibody (A06705-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAD51AP1 antigen affinity purified polyclonal antibody (Catalog # A06705-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAD51AP1 at approximately 38 kDa. The expected band size for RAD51AP1 is at 38 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06705-2-rad51ap1-primary-antibodies-ihc-testing-2.jpgAnti-RAD51AP1 Antibody Picoband® IHC analysis of RAD51AP1 using anti-RAD51AP1 antibody (A06705-2). RAD51AP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAD51AP1 Antibody (A06705-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06705-2-rad51ap1-primary-antibodies-ihc-testing-3.jpgAnti-RAD51AP1 Antibody Picoband® IHC analysis of RAD51AP1 using anti-RAD51AP1 antibody (A06705-2). RAD51AP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAD51AP1 Antibody (A06705-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06705-2-rad51ap1-primary-antibodies-if-testing-4.jpgAnti-RAD51AP1 Antibody Picoband® IF analysis of RAD51AP1 using anti-RAD51AP1 antibody (A06705-2) and anti-Beta Tubulin antibody (M01857-3). RAD51AP1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RAD51AP1 Antibody (A06705-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06705-2-rad51ap1-primary-antibodies-fcm-testing-5.jpgAnti-RAD51AP1 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-RAD51AP1 antibody (A06705-2). Overlay histogram showing Caco-2 cells stained with A06705-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAD51AP1 Antibody (A06705-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264682026-03-27T05:07:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05585-1-rhbg-primary-antibodies-wb-testing-1.jpgAnti-RHBG Antibody Picoband® Western blot analysis of RHBG using anti-RHBG antibody (A05585-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RHBG antigen affinity purified polyclonal antibody (Catalog # A05585-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RHBG at approximately 47 kDa. The expected band size for RHBG is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05585-1-rhbg-primary-antibodies-fcm-testing-2.jpgAnti-RHBG Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-RHBG antibody (A05585-1). Overlay histogram showing HepG2 cells stained with A05585-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RHBG Antibody (A05585-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05585-1-rhbg-primary-antibodies-fcm-testing-3.jpgAnti-RHBG Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-RHBG antibody (A05585-1). Overlay histogram showing RT4 cells stained with A05585-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RHBG Antibody (A05585-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264692026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12576-1-rtkn2-primary-antibodies-wb-testing-1.jpgAnti-RTKN2 Antibody Picoband® Western blot analysis of RTKN2 using anti-RTKN2 antibody (A12576-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HL-60 whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse lung tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RTKN2 antigen affinity purified polyclonal antibody (Catalog # A12576-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RTKN2 at approximately 69 kDa. The expected band size for RTKN2 is at 69 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12576-1-rtkn2-primary-antibodies-fcm-testing-2.jpgAnti-RTKN2 Antibody Picoband® Flow Cytometry analysis of Raji cells using anti-RTKN2 antibody (A12576-1). Overlay histogram showing Raji cells stained with A12576-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RTKN2 Antibody (A12576-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-marf-dz41514-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-centaurin-b1-a-dz41516-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-myxococcales-bacterium-eoo73-05625-dz41538-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-candidatus-entotheonella-gemina-etsy2-08400-dz41540-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-mertka-dz41553-boster.html2026-03-17T05:16:12+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-axolotl-msx1-dz41558-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-acomys-ptprc-dz41559-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-epstein-barr-virus-bclf1-dz41560-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-epstein-barr-virus-borf1-dz41561-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-epstein-barr-virus-bdrf1-dz41562-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-epstein-barr-virus-bfrf1-dz41563-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-epstein-barr-virus-bfrf2-dz41564-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-epstein-barr-virus-bnrf1-dz41565-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-dsn1-dz41567-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-mad-dz41570-boster.html2026-03-10T04:37:40+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1264862026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10377-1-pyhin1-primary-antibodies-wb-testing-1_1.jpgAnti-PYHIN1 Antibody Picoband®Western blot analysis of PYHIN1 using anti-PYHIN1 antibody (A10377-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human Jurkat whole cell lysates. Lane 3: human HEL whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse A20 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PYHIN1 antigen affinity purified polyclonal antibody (Catalog # A10377-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PYHIN1 at approximately 55 kDa. The expected band size for PYHIN1 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10377-1-pyhin1-primary-antibodies-ihc-testing-1.jpgAnti-PYHIN1 Antibody Picoband®IHC analysis of PYHIN1 using anti-PYHIN1 antibody (A10377-1). PYHIN1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PYHIN1 Antibody (A10377-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10377-1-pyhin1-primary-antibodies-if-testing-1.jpgAnti-PYHIN1 Antibody Picoband®IF analysis of PYHIN1 using anti-PYHIN1 antibody (A10377-1) and anti-Tubulin Alpha antibody (M03989-3). PYHIN1 was detected in immunocytochemical section of SiHa cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PYHIN1 Antibody (A10377-1) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10377-1-pyhin1-primary-antibodies-fcm-testing-1.jpgAnti-PYHIN1 Antibody Picoband®Flow Cytometry analysis of THP-1 cells using anti-PYHIN1 antibody (A10377-1). Overlay histogram showing THP-1 cells stained with A10377-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PYHIN1 Antibody (A10377-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264872026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04671-2-ankrd1-primary-antibodies-wb-testing-1.jpgAnti-ANKRD1 Antibody Picoband® Western blot analysis of ANKRD1 using anti-ANKRD1 antibody (A04671-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ANKRD1 antigen affinity purified polyclonal antibody (Catalog # A04671-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ANKRD1 at approximately 36 kDa. The expected band size for ANKRD1 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04671-2-ankrd1-primary-antibodies-fcm-testing-2.jpgAnti-ANKRD1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ANKRD1 antibody (A04671-2). Overlay histogram showing HepG2 cells stained with A04671-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ANKRD1 Antibody (A04671-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264882026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11807-rtl1-primary-antibodies-wb-testing-1.jpgAnti-RTL1 Antibody Picoband® Western blot analysis of RTL1 using anti-RTL1 antibody (A11807). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RTL1 antigen affinity purified polyclonal antibody (Catalog # A11807) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RTL1 at approximately 200 kDa. The expected band size for RTL1 is at 155 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11807-rtl1-primary-antibodies-fcm-testing-2.jpgAnti-RTL1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-RTL1 antibody (A11807). Overlay histogram showing SH-SY5Y cells stained with A11807 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RTL1 Antibody (A11807, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264892026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11249-1-synj2bp-primary-antibodies-wb-testing-1.jpgAnti-SYNJ2BP Antibody Picoband® Western blot analysis of SYNJ2BP using anti-SYNJ2BP antibody (A11249-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SYNJ2BP antigen affinity purified polyclonal antibody (Catalog # A11249-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SYNJ2BP at approximately 16 kDa. The expected band size for SYNJ2BP is at 16 kDa. https://www.bosterbio.com/catalog/product/view/id/1264902026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04679-noxa1-primary-antibodies-wb-testing-1.jpgAnti-NOXA1 Antibody Picoband® Western blot analysis of NOXA1 using anti-NOXA1 antibody (A04679). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOXA1 antigen affinity purified polyclonal antibody (Catalog # A04679) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOXA1 at approximately 60 kDa. The expected band size for NOXA1 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04679-noxa1-primary-antibodies-wb-testing-2.jpgAnti-NOXA1 Antibody Picoband® Western blot analysis of NOXA1 using anti-NOXA1 antibody (A04679). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOXA1 antigen affinity purified polyclonal antibody (Catalog # A04679) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOXA1 at approximately 60 kDa. The expected band size for NOXA1 is at 51 kDa. https://www.bosterbio.com/catalog/product/view/id/1264912026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14266-1-synpo2l-primary-antibodies-wb-testing-1.jpgAnti-SYNPO2L Antibody Picoband® Western blot analysis of SYNPO2L using anti-SYNPO2L antibody (A14266-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: rat testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SYNPO2L antigen affinity purified polyclonal antibody (Catalog # A14266-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SYNPO2L at approximately 102 kDa. The expected band size for SYNPO2L is at 102 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14266-1-synpo2l-primary-antibodies-fcm-testing-2.jpgAnti-SYNPO2L Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-SYNPO2L antibody (A14266-1). Overlay histogram showing SH-SY5Y cells stained with A14266-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SYNPO2L Antibody (A14266-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264922026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02343-1-rps19-primary-antibodies-wb-testing-1.jpgAnti-RPS19 Antibody Picoband® Western blot analysis of RPS19 using anti-RPS19 antibody (A02343-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS19 antigen affinity purified polyclonal antibody (Catalog # A02343-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPS19 at approximately 16 kDa. The expected band size for RPS19 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02343-1-rps19-primary-antibodies-if-testing-2.jpgAnti-RPS19 Antibody Picoband® IF analysis of RPS19 using anti-RPS19 antibody (A02343-1). RPS19 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RPS19 Antibody (A02343-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02343-1-rps19-primary-antibodies-fcm-testing-3.jpgAnti-RPS19 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-RPS19 antibody (A02343-1). Overlay histogram showing 293T cells stained with A02343-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPS19 Antibody (A02343-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02343-1-rps19-primary-antibodies-ip-testing-1.jpgAnti-RPS19 Antibody Picoband®Immunoprecipitating (IP) RPS19 in K562 whole cell lysate. Western blot analysis of RPS19 using anti-RPS19 antibody (A02343-1); Lane 1: K562 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-RPS19 antibody in K562 whole cell lysate; Lane 3: anti-RPS19 antibody (2μg) + K562 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RPS19 antigen affinity purified polyclonal antibody (A02343-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for RPS19 at approximately 16 kDa. The expected band size for RPS19 is at 16 kDa. https://www.bosterbio.com/catalog/product/view/id/1264932026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01250-3-eno1-primary-antibodies-wb-testing-1.jpgAnti-ENO1 Antibody Picoband® Western blot analysis of ENO1 using anti-ENO1 antibody (A01250-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ENO1 antigen affinity purified polyclonal antibody (Catalog # A01250-3) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ENO1 at approximately 47 kDa. The expected band size for ENO1 is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01250-3-eno1-primary-antibodies-ihc-testing-1.jpgAnti-ENO1 Antibody Picoband®IHC analysis of ENO1 using anti-ENO1 antibody (A01250-3). ENO1 was detected in a paraffin-embedded section of human cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ENO1 Antibody (A01250-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01250-3-eno1-primary-antibodies-ihc-testing-2.jpgAnti-ENO1 Antibody Picoband® IHC analysis of ENO1 using anti-ENO1 antibody (A01250-3). ENO1 was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ENO1 Antibody (A01250-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01250-3-eno1-primary-antibodies-ihc-testing-3.jpgAnti-ENO1 Antibody Picoband® IHC analysis of ENO1 using anti-ENO1 antibody (A01250-3). ENO1 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ENO1 Antibody (A01250-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01250-3-eno1-primary-antibodies-fcm-testing-4.jpgAnti-ENO1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-ENO1 antibody (A01250-3). Overlay histogram showing A549 cells stained with A01250-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ENO1 Antibody (A01250-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01250-3-eno1-primary-antibodies-fcm-testing-5.jpgAnti-ENO1 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-ENO1 antibody (A01250-3). Overlay histogram showing Hela cells stained with A01250-3 (Blue line). The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ENO1 Antibody (A01250-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264942026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-wb-testing-1.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® Western blot analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Annexin A1/ANXA1 antigen affinity purified polyclonal antibody (Catalog # A01451-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Annexin A1/ANXA1 at approximately 35 kDa. The expected band size for Annexin A1/ANXA1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-wb-testing-2.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® Western blot analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Annexin A1/ANXA1 antigen affinity purified polyclonal antibody (Catalog # A01451-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for Annexin A1/ANXA1 at approximately 35 kDa. The expected band size for Annexin A1/ANXA1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-3.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-4.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-5.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-6.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-7.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of human testis cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-8.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-9.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of mouse lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-ihc-testing-10.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IHC analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in a paraffin-embedded section of rat lung tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-if-testing-11.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® IF analysis of Annexin A1/ANXA1 using anti-Annexin A1/ANXA1 antibody (A01451-1). Annexin A1/ANXA1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01451-1-anxa1-primary-antibodies-fcm-testing-12.jpgAnti-Annexin A1/ANXA1 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-Annexin A1/ANXA1 antibody (A01451-1). Overlay histogram showing A431 cells stained with A01451-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Annexin A1/ANXA1 Antibody (A01451-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264952026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15361-1-ogfod3-primary-antibodies-wb-testing-1.jpgAnti-OGFOD3 Antibody Picoband® Western blot analysis of OGFOD3 using anti-OGFOD3 antibody (A15361-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse brain tissue lysates, Lane 4: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OGFOD3 antigen affinity purified polyclonal antibody (Catalog # A15361-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OGFOD3 at approximately 36 kDa. The expected band size for OGFOD3 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15361-1-ogfod3-primary-antibodies-ihc-testing-1.jpgAnti-OGFOD3 Antibody Picoband®IHC analysis of OGFOD3 using anti-OGFOD3 antibody (A15361-1). OGFOD3 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-OGFOD3 Antibody (A15361-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15361-1-ogfod3-primary-antibodies-if-testing-2.jpgAnti-OGFOD3 Antibody Picoband® IF analysis of OGFOD3 using anti-OGFOD3 antibody (A15361-1) and anti-Beta Tubulin antibody (M01857-3). OGFOD3 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-OGFOD3 Antibody (A15361-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15361-1-ogfod3-primary-antibodies-fcm-testing-3.jpgAnti-OGFOD3 Antibody Picoband® Flow Cytometry analysis of MOLT-4 cells using anti-OGFOD3 antibody (A15361-1). Overlay histogram showing MOLT-4 cells stained with A15361-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-OGFOD3 Antibody (A15361-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15361-1-ogfod3-primary-antibodies-fcm-testing-4.jpgAnti-OGFOD3 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-OGFOD3 antibody (A15361-1). Overlay histogram showing SiHa cells stained with A15361-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-OGFOD3 Antibody (A15361-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264962026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09235-1-p3h2-primary-antibodies-wb-testing-1.jpgAnti-P3H2 Antibody Picoband® Western blot analysis of P3H2 using anti-P3H2 antibody (A09235-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P3H2 antigen affinity purified polyclonal antibody (Catalog # A09235-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for P3H2 at approximately 81 kDa. The expected band size for P3H2 is at 81,60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09235-1-p3h2-primary-antibodies-ihc-testing-2.jpgAnti-P3H2 Antibody Picoband® IHC analysis of P3H2 using anti-P3H2 antibody (A09235-1). P3H2 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-P3H2 Antibody (A09235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09235-1-p3h2-primary-antibodies-ihc-testing-3.jpgAnti-P3H2 Antibody Picoband® IHC analysis of P3H2 using anti-P3H2 antibody (A09235-1). P3H2 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-P3H2 Antibody (A09235-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09235-1-p3h2-primary-antibodies-if-testing-4.jpgAnti-P3H2 Antibody Picoband® IF analysis of P3H2 using anti-P3H2 antibody (A09235-1) and anti-Beta Tubulin antibody (M01857-3). P3H2 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-P3H2 Antibody (A09235-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1142) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09235-1-p3h2-primary-antibodies-fcm-testing-5.jpgAnti-P3H2 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-P3H2 antibody (A09235-1). Overlay histogram showing RT4 cells stained with A09235-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-P3H2 Antibody (A09235-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264972026-03-17T05:16:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09573-2-pdlim4-primary-antibodies-wb-testing-1.jpgAnti-PDLIM4 Antibody Picoband® Western blot analysis of PDLIM4 using anti-PDLIM4 antibody (A09573-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDLIM4 antigen affinity purified polyclonal antibody (Catalog # A09573-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PDLIM4 at approximately 35 kDa. The expected band size for PDLIM4 is at 35,26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09573-2-pdlim4-primary-antibodies-if-testing-2.jpgAnti-PDLIM4 Antibody Picoband® IF analysis of PDLIM4 using anti-PDLIM4 antibody (A09573-2). PDLIM4 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PDLIM4 Antibody (A09573-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09573-2-pdlim4-primary-antibodies-fcm-testing-3.jpgAnti-PDLIM4 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-PDLIM4 antibody (A09573-2). Overlay histogram showing A431 cells stained with A09573-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PDLIM4 Antibody (A09573-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09573-2-pdlim4-primary-antibodies-wb-testing-4.jpgAnti-PDLIM4 Antibody Picoband® Western blot analysis of PDLIM4 using anti-PDLIM4 antibody (A09573-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PDLIM4 antigen affinity purified polyclonal antibody (A09573-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for PDLIM4 at approximately 37 kDa. The expected band size for PDLIM4 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09573-2-pdlim4-primary-antibodies-ip-testing-5.jpgAnti-PDLIM4 Antibody Picoband® Immunoprecipitating (IP) PDLIM4 in U251 whole cell lysate. Western blot analysis of PDLIM4 using anti-PDLIM4 antibody (A09573-2); Lane 1: U251 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-PDLIM4 antibody in U251 whole cell lysate; Lane 3: anti-PDLIM4 antibody (2μg) + U251 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PDLIM4 antigen affinity purified polyclonal antibody (A09573-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PDLIM4 at approximately 37 kDa. The expected band size for PDLIM4 is at 35 kDa. https://www.bosterbio.com/catalog/product/view/id/1264982026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00921-1-egr2-primary-antibodies-wb-testing-1.jpgAnti-EGR2 Antibody Picoband® Western blot analysis of EGR2 using anti-EGR2 antibody (A00921-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EGR2 antigen affinity purified polyclonal antibody (Catalog # A00921-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EGR2 at approximately 50 kDa. The expected band size for EGR2 is at 50,45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00921-1-egr2-primary-antibodies-fcm-testing-2.jpgAnti-EGR2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-EGR2 antibody (A00921-1). Overlay histogram showing MCF-7 cells stained with A00921-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EGR2 Antibody (A00921-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1264992026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03618-2-hspa4-primary-antibodies-wb-testing-1.jpgAnti-HSPA4 Antibody Picoband® Western blot analysis of HSPA4 using anti-HSPA4 antibody (A03618-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse NIH/3T3 whole cell lysates, Lane 8: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA4 antigen affinity purified polyclonal antibody (Catalog # A03618-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for HSPA4 at approximately 110 kDa. The expected band size for HSPA4 is at 96,14 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03618-2-hspa4-primary-antibodies-wb-testing-2.jpgAnti-HSPA4 Antibody Picoband® Western blot analysis of HSPA4 using anti-HSPA4 antibody (A03618-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates, Lane 7: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HSPA4 antigen affinity purified polyclonal antibody (Catalog # A03618-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HSPA4 at approximately 110 kDa. The expected band size for HSPA4 is at 94,16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03618-2-hspa4-primary-antibodies-ihc-testing-3.jpgAnti-HSPA4 Antibody Picoband® IHC analysis of HSPA4 using anti-HSPA4 antibody (A03618-2). HSPA4 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSPA4 Antibody (A03618-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03618-2-hspa4-primary-antibodies-ihc-testing-4.jpgAnti-HSPA4 Antibody Picoband® IHC analysis of HSPA4 using anti-HSPA4 antibody (A03618-2). HSPA4 was detected in a paraffin-embedded section of mouse ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-HSPA4 Antibody (A03618-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03618-2-hspa4-primary-antibodies-fcm-testing-5.jpgAnti-HSPA4 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-HSPA4 antibody (A03618-2). Overlay histogram showing 293T cells stained with A03618-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSPA4 Antibody (A03618-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03618-2-hspa4-primary-antibodies-fcm-testing-6.jpgAnti-HSPA4 Antibody Picoband® Flow Cytometry analysis of MOLT-4 cells using anti-HSPA4 antibody (A03618-2). Overlay histogram showing MOLT-4 cells stained with A03618-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HSPA4 Antibody (A03618-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265002026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03989-2-tubulin-alpha-primary-antibodies-wb-testing-1.jpgAnti-Alpha Tubulin/TUBA1C Antibody Picoband® Western blot analysis of Tubulin Alpha using anti-Tubulin Alpha antibody (A03989-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: rat liver tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Tubulin Alpha antigen affinity purified polyclonal antibody (Catalog # A03989-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Tubulin Alpha at approximately 55 kDa. The expected band size for Tubulin Alpha is at 50 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03989-2-tubulin-alpha-primary-antibodies-ihc-testing-2.jpgAnti-Alpha Tubulin/TUBA1C Antibody Picoband® IHC analysis of Tubulin Alpha using anti-Tubulin Alpha antibody (A03989-2). Tubulin Alpha was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Tubulin Alpha Antibody (A03989-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03989-2-tubulin-alpha-primary-antibodies-ihc-testing-3.jpgAnti-Alpha Tubulin/TUBA1C Antibody Picoband® IHC analysis of Tubulin Alpha using anti-Tubulin Alpha antibody (A03989-2). Tubulin Alpha was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Tubulin Alpha Antibody (A03989-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03989-2-tubulin-alpha-primary-antibodies-ihc-testing-4.jpgAnti-Alpha Tubulin/TUBA1C Antibody Picoband® IHC analysis of Tubulin Alpha using anti-Tubulin Alpha antibody (A03989-2). Tubulin Alpha was detected in a paraffin-embedded section of human urothelial carcinoma with squamous differentiation tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Tubulin Alpha Antibody (A03989-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03989-2-tubulin-alpha-primary-antibodies-if-testing-5.jpgAnti-Alpha Tubulin/TUBA1C Antibody Picoband® IF analysis of Tubulin Alpha using anti-Tubulin Alpha antibody (A03989-2). Tubulin Alpha was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Tubulin Alpha Antibody (A03989-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03989-2-tubulin-alpha-primary-antibodies-fcm-testing-6.jpgAnti-Alpha Tubulin/TUBA1C Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-Tubulin Alpha antibody (A03989-2). Overlay histogram showing 293T cells stained with A03989-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Tubulin Alpha Antibody (A03989-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265012026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07543-3-osbpl2-primary-antibodies-wb-testing-1.jpgAnti-OSBPL2 Antibody Picoband® Western blot analysis of OSBPL2 using anti-OSBPL2 antibody (A07543-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OSBPL2 antigen affinity purified polyclonal antibody (Catalog # A07543-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OSBPL2 at approximately 55 kDa. The expected band size for OSBPL2 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07543-3-osbpl2-primary-antibodies-if-testing-2.jpgAnti-OSBPL2 Antibody Picoband® IF analysis of OSBPL2 using anti-OSBPL2 antibody (A07543-3). OSBPL2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-OSBPL2 Antibody (A07543-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07543-3-osbpl2-primary-antibodies-fcm-testing-3.jpgAnti-OSBPL2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-OSBPL2 antibody (A07543-3). Overlay histogram showing HepG2 cells stained with A07543-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-OSBPL2 Antibody (A07543-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265022026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07503-2-tbr1-primary-antibodies-wb-testing-1.jpgAnti-TBR1 Antibody Picoband® Western blot analysis of TBR1 using anti-TBR1 antibody (A07503-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: rat brain tissue lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TBR1 antigen affinity purified polyclonal antibody (Catalog # A07503-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TBR1 at approximately 74 kDa. The expected band size for TBR1 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07503-2-tbr1-primary-antibodies-fcm-testing-2.jpgAnti-TBR1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-TBR1 antibody (A07503-2). Overlay histogram showing SH-SY5Y cells stained with A07503-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TBR1 Antibody (A07503-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265032026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06672-1-strn3-primary-antibodies-wb-testing-1.jpgAnti-STRN3 Antibody Picoband® Western blot analysis of STRN3 using anti-STRN3 antibody (A06672-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat H9C2(2-1) whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STRN3 antigen affinity purified polyclonal antibody (Catalog # A06672-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STRN3 at approximately 94 kDa. The expected band size for STRN3 is at 87,78 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06672-1-strn3-primary-antibodies-if-testing-2.jpgAnti-STRN3 Antibody Picoband® IF analysis of STRN3 using anti-STRN3 antibody (A06672-1). STRN3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-STRN3 Antibody (A06672-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06672-1-strn3-primary-antibodies-fcm-testing-3.jpgAnti-STRN3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-STRN3 antibody (A06672-1). Overlay histogram showing HepG2 cells stained with A06672-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-STRN3 Antibody (A06672-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265042026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16683-1-rtfdc1-primary-antibodies-wb-testing-1.jpgAnti-RTF2 Antibody Picoband® Western blot analysis of RTF2 using anti-RTF2 antibody (A16683-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human Siha whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RTF2 antigen affinity purified polyclonal antibody (Catalog # A16683-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RTF2 at approximately 37 kDa. The expected band size for RTF2 is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16683-1-rtfdc1-primary-antibodies-if-testing-2.jpgAnti-RTF2 Antibody Picoband® IF analysis of RTF2 using anti-RTF2 antibody (A16683-1) and anti-Beta Tubulin antibody (M01857-3). RTF2 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RTF2 Antibody (A16683-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16683-1-rtfdc1-primary-antibodies-fcm-testing-3.jpgAnti-RTF2 Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-RTF2 antibody (A16683-1). Overlay histogram showing U87 cells stained with A16683-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RTF2 Antibody (A16683-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16683-1-rtf2-primary-antibodies-ip-testing-4.jpgAnti-RTF2 Antibody Picoband® Immunoprecipitating RTF2 in MCF-7 whole cell lysate. Western blot analysis of RTF2 using anti-RTF2 antibody (A16683-1); Lane 1: MCF-7 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-RTF2 antibody in MCF-7 whole cell lysate; Lane 3: anti-RTF2 antibody (2μg) + MCF-7 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RTF2 antigen affinity purified polyclonal antibody (A16683-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for RTF2 at approximately 37 kDa. The expected band size for RTF2 is at 34 kDa. https://www.bosterbio.com/catalog/product/view/id/1265052026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07675-1-pls1-primary-antibodies-wb-testing-1.jpgAnti-PLS1 Antibody Picoband® Western blot analysis of PLS1 using anti-PLS1 antibody (A07675-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat small intestine tissue lysates, Lane 6: rat stomach tissue lysates, Lane 7: mouse small intestine tissue lysates, Lane 8: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLS1 antigen affinity purified polyclonal antibody (Catalog # A07675-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLS1 at approximately 70 kDa. The expected band size for PLS1 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07675-1-pls1-primary-antibodies-ihc-testing-2.jpgAnti-PLS1 Antibody Picoband® IHC analysis of PLS1 using anti-PLS1 antibody (A07675-1). PLS1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLS1 Antibody (A07675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07675-1-pls1-primary-antibodies-ihc-testing-3.jpgAnti-PLS1 Antibody Picoband® IHC analysis of PLS1 using anti-PLS1 antibody (A07675-1). PLS1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLS1 Antibody (A07675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07675-1-pls1-primary-antibodies-ihc-testing-4.jpgAnti-PLS1 Antibody Picoband® IHC analysis of PLS1 using anti-PLS1 antibody (A07675-1). PLS1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLS1 Antibody (A07675-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07675-1-pls1-primary-antibodies-if-testing-5.jpgAnti-PLS1 Antibody Picoband® IF analysis of PLS1 using anti-PLS1 antibody (A07675-1). PLS1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PLS1 Antibody (A07675-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07675-1-pls1-primary-antibodies-fcm-testing-6.jpgAnti-PLS1 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-PLS1 antibody (A07675-1). Overlay histogram showing RT4 cells stained with A07675-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PLS1 Antibody (A07675-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07675-1-pls1-primary-antibodies-wb-testing-7.jpgAnti-PLS1 Antibody Picoband® Western blot analysis of PLS1 using anti-PLS1 antibody (A07675-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: mouse small intestine tissue lysates, Lane 6: rat stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLS1 antigen affinity purified polyclonal antibody (A07675-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for PLS1 at approximately 70 kDa. The expected band size for PLS1 is at 70 kDa. https://www.bosterbio.com/catalog/product/view/id/1265062026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04134-1-pls3-primary-antibodies-wb-testing-1.jpgAnti-PLS3 Antibody Picoband® Western blot analysis of PLS3 using anti-PLS3 antibody (A04134-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human Siha whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat stomach tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse stomach tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLS3 antigen affinity purified polyclonal antibody (Catalog # A04134-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLS3 at approximately 71 kDa. The expected band size for PLS3 is at 71,69,66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04134-1-pls3-primary-antibodies-if-testing-2.jpgAnti-PLS3 Antibody Picoband® IF analysis of PLS3 using anti-PLS3 antibody (A04134-1). PLS3 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PLS3 Antibody (A04134-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04134-1-pls3-primary-antibodies-fcm-testing-3.jpgAnti-PLS3 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-PLS3 antibody (A04134-1). Overlay histogram showing PC-3 cells stained with A04134-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PLS3 Antibody (A04134-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04134-1-pls3-primary-antibodies-wb-testing-4.jpgAnti-PLS3 Antibody Picoband® Western blot analysis of PLS3 using anti-PLS3 antibody (A04134-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: mouse pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLS3 antigen affinity purified polyclonal antibody (A04134-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for PLS3 at approximately 71 kDa. The expected band size for PLS3 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04134-1-pls3-primary-antibodies-ip-testing-5.jpgAnti-PLS3 Antibody Picoband® Immunoprecipitating PLS3 in Hela whole cell lysate. Western blot analysis of PLS3 using anti-PLS3 antibody (A04134-1). Lane 1: Hela whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-PLS3 antibody in Hela whole cell lysate. Lane 3: anti-PLS3 antibody (2μg) + Hela whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PLS3 antigen affinity purified polyclonal antibody (A04134-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PLS3 at approximately 71 kDa. The expected band size for PLS3 is at 71 kDa. https://www.bosterbio.com/catalog/product/view/id/1265072026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00577-1-creb1-primary-antibodies-wb-testing-1.jpgAnti-CREB1 Antibody Picoband® Western blot analysis of CREB1 using anti-CREB1 antibody (A00577-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: monkey COS-7 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CREB1 antigen affinity purified polyclonal antibody (Catalog # A00577-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CREB1 at approximately 43,49 kDa. The expected band size for CREB1 is at 36,37,25 kDa. https://www.bosterbio.com/catalog/product/view/id/1265082026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00859-2-stk4-primary-antibodies-wb-testing-1.jpgAnti-MST1/STK4 Antibody Picoband® Western blot analysis of MST1/STK4 using anti-MST1/STK4 antibody (A00859-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human Ramos whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MST1/STK4 antigen affinity purified polyclonal antibody (Catalog # A00859-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MST1/STK4 at approximately 56 kDa. The expected band size for MST1/STK4 is at 56,52 kDa. https://www.bosterbio.com/catalog/product/view/id/1265092026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07605-1-rere-primary-antibodies-wb-testing-1.jpgAnti-RERE Antibody Picoband® Western blot analysis of RERE using anti-RERE antibody (A07605-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RERE antigen affinity purified polyclonal antibody (Catalog # A07605-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RERE at approximately 170,212 kDa. The expected band size for RERE is at 172,109 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07605-1-rere-primary-antibodies-ihc-testing-2.jpgAnti-RERE Antibody Picoband® IHC analysis of RERE using anti-RERE antibody (A07605-1). RERE was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RERE Antibody (A07605-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07605-1-rere-primary-antibodies-if-testing-3.jpgAnti-RERE Antibody Picoband® IF analysis of RERE using anti-RERE antibody (A07605-1) and anti-Beta Tubulin antibody (M01857-3). RERE was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RERE Antibody (A07605-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07605-1-rere-primary-antibodies-fcm-testing-4.jpgAnti-RERE Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-RERE antibody (A07605-1). Overlay histogram showing HepG2 cells stained with A07605-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RERE Antibody (A07605-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07605-1-rere-primary-antibodies-fcm-testing-5.jpgAnti-RERE Antibody Picoband® Flow Cytometry analysis of U87 cells using anti-RERE antibody (A07605-1). Overlay histogram showing U87 cells stained with A07605-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RERE Antibody (A07605-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265102026-03-17T05:16:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14327-pcdha2-primary-antibodies-wb-testing-1.jpgAnti-PCDHA2 Antibody Picoband® Western blot analysis of PCDHA2 using anti-PCDHA2 antibody (A14327). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHA2 antigen affinity purified polyclonal antibody (Catalog # A14327) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHA2 at approximately 120 kDa. The expected band size for PCDHA2 is at 102,69,87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14327-pcdha2-primary-antibodies-fcm-testing-2.jpgAnti-PCDHA2 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PCDHA2 antibody (A14327). Overlay histogram showing Hela cells stained with A14327 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PCDHA2 Antibody (A14327, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265112026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15832-1-pcdha11-primary-antibodies-wb-testing-1.jpgAnti-PCDHA11 Antibody Picoband® Western blot analysis of PCDHA11 using anti-PCDHA11 antibody (A15832-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PCDHA11 antigen affinity purified polyclonal antibody (Catalog # A15832-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PCDHA11 at approximately 150-170 kDa. The expected band size for PCDHA11 is at 103,88 kDa. https://www.bosterbio.com/catalog/product/view/id/1265122026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00239-2-lgr5-primary-antibodies-wb-testing-1.jpgAnti-LGR5 Antibody Picoband® Western blot analysis of LGR5 using anti-LGR5 antibody (A00239-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human 293T whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LGR5 antigen affinity purified polyclonal antibody (Catalog # A00239-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LGR5 at approximately 130 kDa. The expected band size for LGR5 is at 100,97,92 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00239-2-lgr5-primary-antibodies-ihc-testing-2.jpgAnti-LGR5 Antibody Picoband® IHC analysis of LGR5 using anti-LGR5 antibody (A00239-2). LGR5 was detected in a paraffin-embedded section of mouse small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGR5 Antibody (A00239-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00239-2-lgr5-primary-antibodies-ihc-testing-3.jpgAnti-LGR5 Antibody Picoband® IHC analysis of LGR5 using anti-LGR5 antibody (A00239-2). LGR5 was detected in a paraffin-embedded section of rat small intestine tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGR5 Antibody (A00239-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00239-2-lgr5-primary-antibodies-ihc-testing-4.jpgAnti-LGR5 Antibody Picoband®IHC analysis of LGR5 using anti-LGR5 antibody (A00239-2). LGR5 was detected in a paraffin-embedded section of human kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-LGR5 Antibody (A00239-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00239-2-lgr5-primary-antibodies-fcm-testing-4.jpgAnti-LGR5 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-LGR5 antibody (A00239-2). Overlay histogram showing 293T cells stained with A00239-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LGR5 Antibody (A00239-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265132026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01840-2-ror2-primary-antibodies-wb-testing-1.jpgAnti-ROR2 Antibody Picoband® Western blot analysis of ROR2 using anti-ROR2 antibody (A01840-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat small intestine tissue lysates, Lane 6: rat ovary tissue lysates, Lane 8: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ROR2 antigen affinity purified polyclonal antibody (Catalog # A01840-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ROR2 at approximately 105 kDa. The expected band size for ROR2 is at 105 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01840-2-ror2-primary-antibodies-fcm-testing-2.jpgAnti-ROR2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-ROR2 antibody (A01840-2). Overlay histogram showing K562 cells stained with A01840-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ROR2 Antibody (A01840-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01840-2-ror2-primary-antibodies-fcm-testing-3.jpgAnti-ROR2 Antibody Picoband® Flow Cytometry analysis of Raji cells using anti-ROR2 antibody (A01840-2). Overlay histogram showing Raji cells stained with A01840-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ROR2 Antibody (A01840-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265142026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05268-1-rps3a-primary-antibodies-wb-testing-1_1.jpgAnti-RPS3A Antibody Picoband®Western blot analysis of RPS3A using anti-RPS3A antibody (A05268-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat H9C2 whole cell lysates, Lane 7: mouse lung tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS3A antigen affinity purified polyclonal antibody (Catalog # A05268-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for RPS3A at approximately 35 kDa. The expected band size for RPS3A is at 30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05268-1-rps3a-primary-antibodies-if-testing-1.jpgAnti-RPS3A Antibody Picoband®IF analysis of RPS3A using anti-RPS3A antibody (A05268-1). RPS3A was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RPS3A Antibody (A05268-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05268-1-rps3a-primary-antibodies-fcm-testing-1.jpgAnti-RPS3A Antibody Picoband®Flow Cytometry analysis of A431 cells using anti-RPS3A antibody (A05268-1). Overlay histogram showing A431 cells stained with A05268-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPS3A Antibody (A05268-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265152026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05439-2-rrn3-primary-antibodies-wb-testing-1.jpgAnti-RRN3 Antibody Picoband® Western blot analysis of RRN3 using anti-RRN3 antibody (A05439-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RRN3 antigen affinity purified polyclonal antibody (Catalog # A05439-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RRN3 at approximately 74 kDa. The expected band size for RRN3 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05439-2-rrn3-primary-antibodies-fcm-testing-2.jpgAnti-RRN3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-RRN3 antibody (A05439-2). Overlay histogram showing HepG2 cells stained with A05439-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RRN3 Antibody (A05439-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265162026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10068-2-rps21-primary-antibodies-wb-testing-1.jpgAnti-RPS21 Antibody Picoband® Western blot analysis of RPS21 using anti-RPS21 antibody (A10068-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat stomach tissue lysates, Lane 6: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPS21 antigen affinity purified polyclonal antibody (Catalog # A10068-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPS21 at approximately 13 kDa. The expected band size for RPS21 is at 9 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10068-2-rps21-primary-antibodies-ihc-testing-1.jpgAnti-RPS21 Antibody Picoband®IHC analysis of RPS21 using anti-RPS21 antibody (A10068-2). RPS21 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RPS21 Antibody (A10068-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10068-2-rps21-primary-antibodies-if-testing-2.jpgAnti-RPS21 Antibody Picoband® IF analysis of RPS21 using anti-RPS21 antibody (A10068-2). RPS21 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RPS21 Antibody (A10068-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10068-2-rps21-primary-antibodies-fcm-testing-3.jpgAnti-RPS21 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-RPS21 antibody (A10068-2). Overlay histogram showing HepG2 cells stained with A10068-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPS21 Antibody (A10068-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265172026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05927-2-plcb2-primary-antibodies-wb-testing-1.jpgAnti-PLCB2 Antibody Picoband® Western blot analysis of PLCB2 using anti-PLCB2 antibody (A05927-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLCB2 antigen affinity purified polyclonal antibody (Catalog # A05927-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLCB2 at approximately 140 kDa. The expected band size for PLCB2 is at 134 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05927-2-plcb2-primary-antibodies-fcm-testing-2.jpgAnti-PLCB2 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-PLCB2 antibody (A05927-2). Overlay histogram showing THP-1 cells stained with A05927-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PLCB2 Antibody (A05927-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265182026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06554-2-acp2-primary-antibodies-wb-testing-1.jpgAnti-ACP2 Antibody Picoband® Western blot analysis of ACP2 using anti-ACP2 antibody (A06554-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: human 293T whole cell lysates, Lane 6: human A549 whole cell lysates, Lane 7: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACP2 antigen affinity purified polyclonal antibody (Catalog # A06554-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACP2 at approximately 52 kDa. The expected band size for ACP2 is at 48,18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06554-2-acp2-primary-antibodies-wb-testing-2.jpgAnti-ACP2 Antibody Picoband® Western blot analysis of ACP2 using anti-ACP2 antibody (A06554-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat C6 whole cell lysates, Lane 3: mouse brain tissue lysates, Lane 4: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACP2 antigen affinity purified polyclonal antibody (Catalog # A06554-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACP2 at approximately 52 kDa. The expected band size for ACP2 is at 48,18 kDa. https://www.bosterbio.com/catalog/product/view/id/1265192026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06344-1-phactr1-primary-antibodies-wb-testing-1.jpgAnti-PHACTR1 Antibody Picoband® Western blot analysis of PHACTR1 using anti-PHACTR1 antibody (A06344-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHACTR1 antigen affinity purified polyclonal antibody (Catalog # A06344-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHACTR1 at approximately 69 kDa. The expected band size for PHACTR1 is at 66 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06344-1-phactr1-primary-antibodies-fcm-testing-2.jpgAnti-PHACTR1 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-PHACTR1 antibody (A06344-1). Overlay histogram showing A549 cells stained with A06344-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHACTR1 Antibody (A06344-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265202026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14122-1-phyhipl-primary-antibodies-wb-testing-1.jpgAnti-PHYHIPL Antibody Picoband® Western blot analysis of PHYHIPL using anti-PHYHIPL antibody (A14122-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHYHIPL antigen affinity purified polyclonal antibody (Catalog # A14122-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHYHIPL at approximately 40 kDa. The expected band size for PHYHIPL is at 42,40,6 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14122-1-phyhipl-primary-antibodies-fcm-testing-2.jpgAnti-PHYHIPL Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-PHYHIPL antibody (A14122-1). Overlay histogram showing CACO-2 cells stained with A14122-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHYHIPL Antibody (A14122-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265212026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09775-1-pkn3-primary-antibodies-wb-testing-1.jpgAnti-PKN3 Antibody Picoband® Western blot analysis of PKN3 using anti-PKN3 antibody (A09775-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PKN3 antigen affinity purified polyclonal antibody (Catalog # A09775-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PKN3 at approximately 99 kDa. The expected band size for PKN3 is at 99 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09775-1-pkn3-primary-antibodies-if-testing-2.jpgAnti-PKN3 Antibody Picoband® IF analysis of PKN3 using anti-PKN3 antibody (A09775-1). PKN3 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PKN3 Antibody (A09775-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09775-1-pkn3-primary-antibodies-fcm-testing-3.jpgAnti-PKN3 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-PKN3 antibody (A09775-1). Overlay histogram showing THP-1 cells stained with A09775-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PKN3 Antibody (A09775-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265222026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14197-1-pld5-primary-antibodies-wb-testing-1.jpgAnti-PLD5 Antibody Picoband® Western blot analysis of PLD5 using anti-PLD5 antibody (A14197-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse Neoro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLD5 antigen affinity purified polyclonal antibody (Catalog # A14197-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLD5 at approximately 69 kDa. The expected band size for PLD5 is at 61,51,38,54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14197-1-pld5-primary-antibodies-ihc-testing-2.jpgAnti-PLD5 Antibody Picoband® IHC analysis of PLD5 using anti-PLD5 antibody (A14197-1). PLD5 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLD5 Antibody (A14197-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14197-1-pld5-primary-antibodies-ihc-testing-3.jpgAnti-PLD5 Antibody Picoband® IHC analysis of PLD5 using anti-PLD5 antibody (A14197-1). PLD5 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLD5 Antibody (A14197-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14197-1-pld5-primary-antibodies-ihc-testing-4.jpgAnti-PLD5 Antibody Picoband® IHC analysis of PLD5 using anti-PLD5 antibody (A14197-1). PLD5 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLD5 Antibody (A14197-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14197-1-pld5-primary-antibodies-ihc-testing-5.jpgAnti-PLD5 Antibody Picoband® IHC analysis of PLD5 using anti-PLD5 antibody (A14197-1). PLD5 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLD5 Antibody (A14197-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14197-1-pld5-primary-antibodies-ihc-testing-6.jpgAnti-PLD5 Antibody Picoband® IHC analysis of PLD5 using anti-PLD5 antibody (A14197-1). PLD5 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PLD5 Antibody (A14197-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14197-1-pld5-primary-antibodies-fcm-testing-7.jpgAnti-PLD5 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-PLD5 antibody (A14197-1). Overlay histogram showing SH-SY5Y cells stained with A14197-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PLD5 Antibody (A14197-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265232026-03-17T05:16:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01041-ednrb-primary-antibodies-wb-testing-1.jpgAnti-EDNRB Antibody Picoband® Western blot analysis of EDNRB using anti-EDNRB antibody (A01041). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EDNRB antigen affinity purified polyclonal antibody (Catalog # A01041) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for EDNRB at approximately 45 kDa. The expected band size for EDNRB is at 49,59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01041-ednrb-primary-antibodies-fcm-testing-2.jpgAnti-EDNRB Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-EDNRB antibody (A01041). Overlay histogram showing CACO-2 cells stained with A01041 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-EDNRB Antibody (A01041, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265242026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01583-5-gdf15-primary-antibodies-wb-testing-1.jpgAnti-Gdf15 Antibody Picoband® Western blot analysis of Gdf15 using anti-Gdf15 antibody (A01583-5). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: rat RH35 whole cell lysates, Lane 4: mouse liver tissue lysates, Lane 5: mouse kidney tissue lysates, Lane 6: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Gdf15 antigen affinity purified polyclonal antibody (Catalog # A01583-5) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Gdf15 at approximately 34 kDa. The expected band size for Gdf15 is at 34,12 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01583-5-gdf15-primary-antibodies-fcm-testing-2.jpgAnti-Gdf15 Antibody Picoband® Flow Cytometry analysis of EL-4 cells using anti-Gdf15 antibody (A01583-5). Overlay histogram showing EL-4 cells stained with A01583-5 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Gdf15 Antibody (A01583-5, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265252026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05348-1-lmnb2-primary-antibodies-wb-testing-1.jpgAnti-Lamin B2/LMNB2 Antibody Picoband® Western blot analysis of Lamin B2/LMNB2 using anti-Lamin B2/LMNB2 antibody (A05348-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Raji whole cell lysates, Lane 4: human Hacat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Lamin B2/LMNB2 antigen affinity purified polyclonal antibody (Catalog # A05348-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Lamin B2/LMNB2 at approximately 72 kDa. The expected band size for Lamin B2/LMNB2 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05348-1-lmnb2-primary-antibodies-ihc-testing-2.jpgAnti-Lamin B2/LMNB2 Antibody Picoband® IHC analysis of Lamin B2/LMNB2 using anti-Lamin B2/LMNB2 antibody (A05348-1). Lamin B2/LMNB2 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lamin B2/LMNB2 Antibody (A05348-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05348-1-lmnb2-primary-antibodies-ihc-testing-3.jpgAnti-Lamin B2/LMNB2 Antibody Picoband® IHC analysis of Lamin B2/LMNB2 using anti-Lamin B2/LMNB2 antibody (A05348-1). Lamin B2/LMNB2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lamin B2/LMNB2 Antibody (A05348-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05348-1-lmnb2-primary-antibodies-ihc-testing-4.jpgAnti-Lamin B2/LMNB2 Antibody Picoband® IHC analysis of Lamin B2/LMNB2 using anti-Lamin B2/LMNB2 antibody (A05348-1). Lamin B2/LMNB2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Lamin B2/LMNB2 Antibody (A05348-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05348-1-lmnb2-primary-antibodies-fcm-testing-5.jpgAnti-Lamin B2/LMNB2 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-Lamin B2/LMNB2 antibody (A05348-1). Overlay histogram showing THP-1 cells stained with A05348-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Lamin B2/LMNB2 Antibody (A05348-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265262026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11546-1-panx3-primary-antibodies-wb-testing-1.jpgAnti-PANX3 Antibody Picoband® Western blot analysis of PANX3 using anti-PANX3 antibody (A11546-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PANX3 antigen affinity purified polyclonal antibody (Catalog # A11546-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PANX3 at approximately 45 kDa. The expected band size for PANX3 is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11546-1-panx3-primary-antibodies-fcm-testing-2.jpgAnti-PANX3 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PANX3 antibody (A11546-1). Overlay histogram showing MCF-7 cells stained with A11546-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PANX3 Antibody (A11546-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11546-1-panx3-primary-antibodies-ip-testing-3.jpgAnti-PANX3 Antibody Picoband® Immunoprecipitating (IP) PANX3 in MCF-7 whole cell lysate. Western blot analysis of PANX3 using anti-PANX3 antibody (A11546-1); Lane 1: MCF-7 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-PANX3 antibody in MCF-7 whole cell lysate; Lane 3: anti-PANX3 antibody (2μg) + MCF-7 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-PANX3 antigen affinity purified polyclonal antibody (A11546-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for PANX3 at approximately 45 kDa. The expected band size for PANX3 is at 45 kDa. https://www.bosterbio.com/catalog/product/view/id/1265272026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12964-1-phyhd1-primary-antibodies-wb-testing-1.jpgAnti-PHYHD1 Antibody Picoband® Western blot analysis of PHYHD1 using anti-PHYHD1 antibody (A12964-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat kidney tissue lysates, Lane 3: mouse liver tissue lysates, Lane 4: mouse kidney tissue lysates, Lane 5: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHYHD1 antigen affinity purified polyclonal antibody (Catalog # A12964-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PHYHD1 at approximately 32 kDa. The expected band size for PHYHD1 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12964-1-phyhd1-primary-antibodies-fcm-testing-2.jpgAnti-PHYHD1 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-PHYHD1 antibody (A12964-1). Overlay histogram showing Hela cells stained with A12964-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHYHD1 Antibody (A12964-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12964-1-phyhd1-primary-antibodies-fcm-testing-3.jpgAnti-PHYHD1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PHYHD1 antibody (A12964-1). Overlay histogram showing HepG2 cells stained with A12964-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHYHD1 Antibody (A12964-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265282026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00006-5-pten-primary-antibodies-wb-testing-1.jpgAnti-PTEN Antibody Picoband® Western blot analysis of PTEN using anti-PTEN antibody (A00006-5). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PTEN antigen affinity purified polyclonal antibody (Catalog # A00006-5) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PTEN at approximately 56 kDa. The expected band size for PTEN is at 47,65,20 kDa. https://www.bosterbio.com/catalog/product/view/id/1265292026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00923-3-ceacam1-primary-antibodies-wb-testing-1.jpgAnti-Ceacam1 Antibody Picoband® Western blot analysis of CEACAM1 using anti-CEACAM1 antibody (A00923-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse Raw264.7 whole cell lysates, Lane 3: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CEACAM1 antigen affinity purified polyclonal antibody (Catalog # A00923-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CEACAM1 at approximately 150 kDa. The expected band size for CEACAM1 is at 57,50,37,30 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00923-3-ceacam1-primary-antibodies-if-testing-2.jpgAnti-Ceacam1 Antibody Picoband® IF analysis of CEACAM1 using anti-CEACAM1 antibody (A00923-3). CEACAM1 was detected in an immunocytochemical section of RAW264.7 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CEACAM1 Antibody (A00923-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00923-3-ceacam1-primary-antibodies-fcm-testing-3.jpgAnti-Ceacam1 Antibody Picoband® Flow Cytometry analysis of HEPA1-6 cells using anti-CEACAM1 antibody (A00923-3). Overlay histogram showing HEPA1-6 cells stained with A00923-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CEACAM1 Antibody (A00923-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00923-3-ceacam1-primary-antibodies-fcm-testing-4.jpgAnti-Ceacam1 Antibody Picoband® Flow Cytometry analysis of RAW264.7 cells using anti-CEACAM1 antibody (A00923-3). Overlay histogram showing RAW264.7 cells stained with A00923-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CEACAM1 Antibody (A00923-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265302026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15197-1-rasl12-primary-antibodies-wb-testing-1.jpgAnti-RASL12 Antibody Picoband® Western blot analysis of RASL12 using anti-RASL12 antibody (A15197-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RASL12 antigen affinity purified polyclonal antibody (Catalog # A15197-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RASL12 at approximately 30 kDa. The expected band size for RASL12 is at 30,29,27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15197-1-rasl12-primary-antibodies-if-testing-2.jpgAnti-RASL12 Antibody Picoband® IF analysis of RASL12 using anti-RASL12 antibody (A15197-1). RASL12 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RASL12 Antibody (A15197-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15197-1-rasl12-primary-antibodies-fcm-testing-3.jpgAnti-RASL12 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-RASL12 antibody (A15197-1). Overlay histogram showing HepG2 cells stained with A15197-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-RASL12 Antibody (A15197-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265312026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09119-plxnb2-primary-antibodies-wb-testing-1.jpgAnti-PLXNB2 Antibody Picoband® Western blot analysis of PLXNB2 using anti-PLXNB2 antibody (A09119). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLXNB2 antigen affinity purified polyclonal antibody (Catalog # A09119) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PLXNB2 at approximately 205 kDa. The expected band size for PLXNB2 is at 205 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09119-plxnb2-primary-antibodies-fcm-testing-2.jpgAnti-PLXNB2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-PLXNB2 antibody (A09119). Overlay histogram showing HepG2 cells stained with A09119 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PLXNB2 Antibody (A09119, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265322026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-3-ace-primary-antibodies-wb-testing-1.jpgAnti-ACE Antibody Picoband® Western blot analysis of ACE using anti-ACE antibody (A00251-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat lung tissue lysates, Lane 2: mouse lung tissue lysates, Lane 3: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACE antigen affinity purified polyclonal antibody (Catalog # A00251-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACE at approximately 150-180 kDa. The expected band size for ACE is at 150 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-3-ace-primary-antibodies-ihc-testing-2.jpgAnti-ACE Antibody Picoband® IHC analysis of ACE using anti-ACE antibody (A00251-3). ACE was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACE Antibody (A00251-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-3-ace-primary-antibodies-ihc-testing-3.jpgAnti-ACE Antibody Picoband® IHC analysis of ACE using anti-ACE antibody (A00251-3). ACE was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACE Antibody (A00251-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-3-ace-primary-antibodies-ihc-testing-4.jpgAnti-ACE Antibody Picoband® IHC analysis of ACE using anti-ACE antibody (A00251-3). ACE was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ACE Antibody (A00251-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00251-3-ace-primary-antibodies-fcm-testing-5.jpgAnti-ACE Antibody Picoband® Flow Cytometry analysis of MOLT-4 cells using anti-ACE antibody (A00251-3). Overlay histogram showing MOLT-4 cells stained with A00251-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ACE Antibody (A00251-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265332026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01963-2-s100p-primary-antibodies-wb-testing-1.jpgAnti-S100P Antibody Picoband® Western blot analysis of S100P using anti-S100P antibody (A01963-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-S100P antigen affinity purified polyclonal antibody (Catalog # A01963-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for S100P at approximately 14 kDa. The expected band size for S100P is at 10 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01963-2-s100p-primary-antibodies-if-testing-2.jpgAnti-S100P Antibody Picoband® IF analysis of S100P using anti-S100P antibody (A01963-2) and anti-Beta Tubulin antibody (M01857-3). S100P was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-S100P Antibody (A01963-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1127) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01963-2-s100p-primary-antibodies-fcm-testing-3.jpgAnti-S100P Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-S100P antibody (A01963-2). Overlay histogram showing SiHa cells stained with A01963-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-S100P Antibody (A01963-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265342026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01128-rs1-primary-antibodies-wb-testing-1.jpgAnti-RS1 Antibody Picoband® Western blot analysis of RS1 using anti-RS1 antibody (A01128). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse eye tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RS1 antigen affinity purified polyclonal antibody (Catalog # A01128) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RS1 at approximately 25 kDa. The expected band size for RS1 is at 25 kDa. https://www.bosterbio.com/catalog/product/view/id/1265352026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02170-2-capn3-primary-antibodies-wb-testing-1.jpgAnti-Calpain 3/CAPN3 Antibody Picoband® Western blot analysis of Calpain 3/CAPN3 using anti-Calpain 3/CAPN3 antibody (A02170-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse thymus tissue lysates, Lane 2: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calpain 3/CAPN3 antigen affinity purified polyclonal antibody (Catalog # A02170-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calpain 3/CAPN3 at approximately 99 kDa. The expected band size for Calpain 3/CAPN3 is at 99 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02170-2-capn3-primary-antibodies-fcm-testing-2.jpgAnti-Calpain 3/CAPN3 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-Calpain 3/CAPN3 antibody (A02170-2). Overlay histogram showing THP-1 cells stained with A02170-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Calpain 3/CAPN3 Antibody (A02170-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265362026-03-17T05:16:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09736-2-rpl27-primary-antibodies-wb-testing-1.jpgAnti-RPL27 Antibody Picoband® Western blot analysis of RPL27 using anti-RPL27 antibody (A09736-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: human RT4 whole cell lysates, Lane 6: human Hela whole cell lysates, Lane 8: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPL27 antigen affinity purified polyclonal antibody (Catalog # A09736-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPL27 at approximately 16 kDa. The expected band size for RPL27 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09736-2-rpl27-primary-antibodies-wb-testing-2.jpgAnti-RPL27 Antibody Picoband® Western blot analysis of RPL27 using anti-RPL27 antibody (A09736-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: rat brain tissue lysates, Lane 3: rat thymus tissue lysates, Lane 4: rat RH35 whole cell lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RPL27 antigen affinity purified polyclonal antibody (Catalog # A09736-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RPL27 at approximately 16 kDa. The expected band size for RPL27 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09736-2-rpl27-primary-antibodies-fcm-testing-3.jpgAnti-RPL27 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-RPL27 antibody (A09736-2). Overlay histogram showing CACO-2 cells stained with A09736-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPL27 Antibody (A09736-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09736-2-rpl27-primary-antibodies-fcm-testing-4.jpgAnti-RPL27 Antibody Picoband® Flow Cytometry analysis of NIH/3T3 cells using anti-RPL27 antibody (A09736-2). Overlay histogram showing NIH/3T3 cells stained with A09736-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPL27 Antibody (A09736-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09736-2-rpl27-primary-antibodies-fcm-testing-5.jpgAnti-RPL27 Antibody Picoband® Flow Cytometry analysis of RH35 cells using anti-RPL27 antibody (A09736-2). Overlay histogram showing RH35 cells stained with A09736-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RPL27 Antibody (A09736-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09736-2-rpl27-primary-antibodies-ip-testing-6.jpgAnti-RPL27 Antibody Picoband® Immunoprecipitating RPL27 in Hela whole cell lysate. Western blot analysis of RPL27 using anti-RPL27 antibody (A09736-2). Lane 1: Hela whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-RPL27 antibody in Hela whole cell lysate. Lane 3: anti-RPL27 antibody (2μg) + Hela whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-RPL27 antigen affinity purified polyclonal antibody (A09736-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for RPL27 at approximately 16 kDa. The expected band size for RPL27 is at 16 kDa. https://www.bosterbio.com/catalog/product/view/id/1265372026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10103-pmvk-primary-antibodies-wb-testing-1_1.jpgAnti-PMVK Antibody Picoband®Western blot analysis of PMVK using anti-PMVK antibody (A10103). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: rat RH35 whole cell lysates, Lane 5: mouse Neuro-2a whole cell lysates, Lane 6: mouse NIH/3T3 whole cell lysates.<br After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PMVK antigen affinity purified polyclonal antibody (A10103) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PMVK at approximately 22 kDa. The expected band size for PMVK is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10103-pmvk-primary-antibodies-if-testing-1.jpgAnti-PMVK Antibody Picoband®IF analysis of PMVK using anti-PMVK antibody (A10103). PMVK was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PMVK Antibody (A10103) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10103-pmvk-primary-antibodies-fcm-testing-1.jpgAnti-PMVK Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-PMVK antibody (A10103). Overlay histogram showing HepG2 cells stained with A10103 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-PMVK Antibody (A10103, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265382026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08694-1-poc1a-primary-antibodies-wb-testing-1.jpgAnti-POC1A Antibody Picoband® Western blot analysis of POC1A using anti-POC1A antibody (A08694-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat thymus tissue lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POC1A antigen affinity purified polyclonal antibody (Catalog # A08694-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POC1A at approximately 40 kDa. The expected band size for POC1A is at 45 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08694-1-poc1a-primary-antibodies-ihc-testing-2.jpgAnti-POC1A Antibody Picoband® IHC analysis of POC1A using anti-POC1A antibody (A08694-1). POC1A was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POC1A Antibody (A08694-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08694-1-poc1a-primary-antibodies-ihc-testing-3.jpgAnti-POC1A Antibody Picoband® IHC analysis of POC1A using anti-POC1A antibody (A08694-1). POC1A was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POC1A Antibody (A08694-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08694-1-poc1a-primary-antibodies-ihc-testing-4.jpgAnti-POC1A Antibody Picoband® IHC analysis of POC1A using anti-POC1A antibody (A08694-1). POC1A was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POC1A Antibody (A08694-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08694-1-poc1a-primary-antibodies-ihc-testing-5.jpgAnti-POC1A Antibody Picoband® IHC analysis of POC1A using anti-POC1A antibody (A08694-1). POC1A was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-POC1A Antibody (A08694-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08694-1-poc1a-primary-antibodies-if-testing-6.jpgAnti-POC1A Antibody Picoband® IF analysis of POC1A using anti-POC1A antibody (A08694-1). POC1A was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-POC1A Antibody (A08694-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08694-1-poc1a-primary-antibodies-fcm-testing-7.jpgAnti-POC1A Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-POC1A antibody (A08694-1). Overlay histogram showing PC-3 cells stained with A08694-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POC1A Antibody (A08694-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265392026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13969-2-ociad2-primary-antibodies-wb-testing-1.jpgAnti-OCIAD2 Antibody Picoband® Western blot analysis of OCIAD2 using anti-OCIAD2 antibody (A13969-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human U20S whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OCIAD2 antigen affinity purified polyclonal antibody (Catalog # A13969-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OCIAD2 at approximately 17 kDa. The expected band size for OCIAD2 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13969-2-ociad2-primary-antibodies-fcm-testing-2.jpgAnti-OCIAD2 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-OCIAD2 antibody (A13969-2). Overlay histogram showing U251 cells stained with A13969-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-OCIAD2 Antibody (A13969-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265402026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02404-4-dvl2-primary-antibodies-wb-testing-1.jpgAnti-DVL2 Antibody Picoband® Western blot analysis of DVL2 using anti-DVL2 antibody (A02404-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DVL2 antigen affinity purified polyclonal antibody (Catalog # A02404-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DVL2 at approximately 85 kDa. The expected band size for DVL2 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02404-4-dvl2-primary-antibodies-fcm-testing-2.jpgAnti-DVL2 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-DVL2 antibody (A02404-4). Overlay histogram showing A431 cells stained with A02404-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DVL2 Antibody (A02404-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265412026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03520-3-bad-primary-antibodies-wb-testing-1.jpgAnti-BAD Antibody Picoband® Western blot analysis of BAD using anti-BAD antibody (A03520-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: mouse Raw264.7 whole cell lysates, Lane 4: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BAD antigen affinity purified polyclonal antibody (Catalog # A03520-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BAD at approximately 22 kDa. The expected band size for BAD is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03520-3-bad-primary-antibodies-fcm-testing-2.jpgAnti-BAD Antibody Picoband® Flow Cytometry analysis of JK cells using anti-BAD antibody (A03520-3). Overlay histogram showing JK cells stained with A03520-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BAD Antibody (A03520-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265422026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05708-1-rnf111-primary-antibodies-wb-testing-1.jpgAnti-RNF111 Antibody Picoband® Western blot analysis of RNF111 using anti-RNF111 antibody (A05708-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RNF111 antigen affinity purified polyclonal antibody (Catalog # A05708-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RNF111 at approximately 109 kDa. The expected band size for RNF111 is at 109 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05708-1-rnf111-primary-antibodies-ihc-testing-4.jpgAnti-RNF111 Antibody Picoband®IHC analysis of RNF111 using anti-RNF111 antibody (A05708-1). RNF111 was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF111 Antibody (A05708-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05708-1-rnf111-primary-antibodies-ihc-testing-2.jpgAnti-RNF111 Antibody Picoband® IHC analysis of RNF111 using anti-RNF111 antibody (A05708-1). RNF111 was detected in a paraffin-embedded section of mouse spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF111 Antibody (A05708-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05708-1-rnf111-primary-antibodies-ihc-testing-3.jpgAnti-RNF111 Antibody Picoband® IHC analysis of RNF111 using anti-RNF111 antibody (A05708-1). RNF111 was detected in a paraffin-embedded section of rat spleen tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RNF111 Antibody (A05708-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05708-1-rnf111-primary-antibodies-if-testing-4.jpgAnti-RNF111 Antibody Picoband® IF analysis of RNF111 using anti-RNF111 antibody (A05708-1) and anti-Beta Tubulin antibody (M01857-3). RNF111 was detected in immunocytochemical section of A549 cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RNF111 Antibody (A05708-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05708-1-rnf111-primary-antibodies-fcm-testing-5.jpgAnti-RNF111 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-RNF111 antibody (A05708-1). Overlay histogram showing SH-SY5Y cells stained with A05708-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RNF111 Antibody (A05708-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265432026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03138-1-odc1-primary-antibodies-wb-testing-1.jpgAnti-ODC1 Antibody Picoband® Western blot analysis of ODC1 using anti-ODC1 antibody (A03138-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human LNCAP whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ODC1 antigen affinity purified polyclonal antibody (Catalog # A03138-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ODC1 at approximately 51 kDa. The expected band size for ODC1 is at 51,55 kDa. https://www.bosterbio.com/catalog/product/view/id/1265442026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08128-2-pitpnm1-primary-antibodies-wb-testing-1.jpgAnti-Nir2/PITPNM1 Antibody Picoband® Western blot analysis of Nir2/PITPNM1 using anti-Nir2/PITPNM1 antibody (A08128-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Nir2/PITPNM1 antigen affinity purified polyclonal antibody (Catalog # A08128-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Nir2/PITPNM1 at approximately 150 kDa. The expected band size for Nir2/PITPNM1 is at 135 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08128-2-pitpnm1-primary-antibodies-fcm-testing-2.jpgAnti-Nir2/PITPNM1 Antibody Picoband® Flow Cytometry analysis of Raji cells using anti-Nir2/PITPNM1 antibody (A08128-2). Overlay histogram showing Raji cells stained with A08128-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Nir2/PITPNM1 Antibody (A08128-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265452026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00565-3-trpv4-primary-antibodies-wb-testing-1.jpgAnti-TRPV4 Antibody Picoband® Western blot analysis of TRPV4 using anti-TRPV4 antibody (A00565-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat testis tissue lysates, Lane 3: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TRPV4 antigen affinity purified polyclonal antibody (Catalog # A00565-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TRPV4 at approximately 100 kDa. The expected band size for TRPV4 is at 98 kDa. https://www.bosterbio.com/catalog/product/view/id/1265462026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05087-3-acsl5-primary-antibodies-wb-testing-1.jpgAnti-ACSL5 Antibody Picoband® Western blot analysis of ACSL5 using anti-ACSL5 antibody (A05087-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ACSL5 antigen affinity purified polyclonal antibody (Catalog # A05087-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ACSL5 at approximately 76 kDa. The expected band size for ACSL5 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05087-3-acsl5-primary-antibodies-if-testing-1.jpgAnti-ACSL5 Antibody Picoband®IF analysis of ACSL5 using anti-ACSL5 antibody (A05087-3). ACSL5 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ACSL5 Antibody (A05087-3) overnight at 4°C. Fluoro488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05087-3-acsl5-primary-antibodies-ip-testing-1.jpgAnti-ACSL5 Antibody Picoband®Immunoprecipitating (IP) ACSL5 in HepG2 whole cell lysate. Western blot analysis of ACSL5 using anti-ACSL5 antibody (A05087-3); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-ACSL5 antibody in HepG2 whole cell lysate; Lane 3: anti-ACSL5 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-ACSL5 antigen affinity purified polyclonal antibody (A05087-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for ACSL5 at approximately 70 kDa. The expected band size for ACSL5 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05087-3-acsl5-primary-antibodies-fcm-testing-2.jpgAnti-ACSL5 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-ACSL5 antibody (A05087-3). Overlay histogram showing Caco-2 cells stained with A05087-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ACSL5 Antibody (A05087-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05087-3-acsl5-primary-antibodies-fcm-testing-3.jpgAnti-ACSL5 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-ACSL5 antibody (A05087-3). Overlay histogram showing Hela cells stained with A05087-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ACSL5 Antibody (A05087-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265472026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00387-2-il2-primary-antibodies-wb-testing-1.jpgAnti-IL2 Antibody Picoband® Western blot analysis of IL2 using anti-IL2 antibody (A00387-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: recombinant human IL-2 protein 10 ng, Lane 2: rat spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IL2 antigen affinity purified polyclonal antibody (Catalog # A00387-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IL2 at approximately 18 kDa. The expected band size for IL2 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00387-2-il2-primary-antibodies-fcm-testing-2.jpgAnti-IL2 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-IL2 antibody (A00387-2). Overlay histogram showing JK cells stained with A00387-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-IL2 Antibody (A00387-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00387-2-il2-primary-antibodies-fcm-testing-3.jpgAnti-IL2 Antibody Picoband® Flow Cytometry analysis of MOLT-4 cells using anti-IL2 antibody (A00387-2). Overlay histogram showing MOLT-4 cells stained with A00387-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-IL2 Antibody (A00387-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265482026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07995-nudt9-primary-antibodies-wb-testing-1.jpgAnti-NUDT9 Antibody Picoband® Western blot analysis of NUDT9 using anti-NUDT9 antibody (A07995). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT9 antigen affinity purified polyclonal antibody (Catalog # A07995) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDT9 at approximately 39 kDa. The expected band size for NUDT9 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07995-nudt9-primary-antibodies-if-testing-2.jpgAnti-NUDT9 Antibody Picoband® IF analysis of NUDT9 using anti-NUDT9 antibody (A07995). NUDT9 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NUDT9 Antibody (A07995) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07995-nudt9-primary-antibodies-fcm-testing-3.jpgAnti-NUDT9 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-NUDT9 antibody (A07995). Overlay histogram showing A431 cells stained with A07995 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDT9 Antibody (A07995, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265492026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11092-2-prdm11-primary-antibodies-wb-testing-1_1.jpgAnti-PRDM11 Antibody Picoband®Western blot analysis of PRDM11 using anti-PRDM11 antibody (A11092-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: rat lung tissue lysates, Lane 7: mouse spleen tissue lysates, Lane 8: mouse lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PRDM11 antigen affinity purified polyclonal antibody (A11092-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PRDM11 at approximately 58 kDa. The expected band size for PRDM11 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11092-2-prdm11-primary-antibodies-ihc-testing-1.jpgAnti-PRDM11 Antibody Picoband®IHC analysis of PRDM11 using anti-PRDM11 antibody (A11092-2). PRDM11 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PRDM11 Antibody (A11092-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11092-2-prdm11-primary-antibodies-ihc-testing-2.jpgAnti-PRDM11 Antibody Picoband®IHC analysis of PRDM11 using anti-PRDM11 antibody (A11092-2). PRDM11 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PRDM11 Antibody (A11092-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11092-2-prdm11-primary-antibodies-if-testing-1.jpgAnti-PRDM11 Antibody Picoband®IF analysis of PRDM11 using anti-PRDM11 antibody (A11092-2) and anti-Tubulin Alpha antibody (M03989-3). PRDM11 was detected in immunocytochemical section of Hela cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PRDM11 Antibody (A11092-2) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11092-2-prdm11-primary-antibodies-if-testing-2_1.jpgAnti-PRDM11 Antibody Picoband®IF analysis of PRDM11 using anti-PRDM11 antibody (A11092-2). PRDM11 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PRDM11 Antibody (A11092-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11092-2-prdm11-primary-antibodies-if-testing-3.jpgAnti-PRDM11 Antibody Picoband®IF analysis of PRDM11 using anti-PRDM11 antibody (A11092-2). PRDM11 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PRDM11 Antibody (A11092-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11092-2-prdm11-primary-antibodies-fcm-testing-1.jpgAnti-PRDM11 Antibody Picoband®Flow Cytometry analysis of THP-1 cells using anti-PRDM11 antibody (A11092-2). Overlay histogram showing THP-1 cells stained with A11092-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PRDM11 Antibody (A11092-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265502026-03-10T04:37:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2283.pngHuman ECM1 ELISA Kit PicoKine®Human ECM1 ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1265512026-03-10T04:37:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2284.pngMouse ECM1 ELISA Kit PicoKine®Mouse ECM1 ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1265522026-03-10T04:37:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2285.pngMouse IFN-Beta ELISA Kit PicoKine®Mouse IFN-Beta ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1265532026-03-10T04:37:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2286.pngHuman IFN-Beta ELISA Kit PicoKine®Human IFN-Beta ELISA Kit PicoKine standard curve https://www.bosterbio.com/products/consumables/cell-culture-flask-cs0002-boster.html2026-03-10T04:37:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0002-cell_culture_flasks-1.jpgCell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0002-cell_culture_flasks-2.jpgCell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0002-cell_culture_flasks-3.jpgCell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0002-cell_culture_flasks-4.jpgCell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0002-cell_culture_flasks-5.jpgCell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0002-cell_culture_flasks-6.jpgCell Culture Flask https://www.bosterbio.com/products/primary-antibodies/anti-human-momo-methyl-paxx-leu139-dz41548-boster.html2026-03-10T04:37:43+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-prominin-1-isoform-x1-prom1b-dz41551-boster.html2026-03-17T05:16:16+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-gip-dz41555-boster.html2026-03-10T04:37:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-re08173p-dmel-tg-dz41557-boster.html2026-03-10T04:37:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-cenp-s-dz41569-boster.html2026-03-10T04:37:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-chlamydomonas-smithii-crptch1-seq1-dz41573-boster.html2026-03-10T04:37:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-turquoise-killifish-sglt2-dz41576-boster.html2026-03-10T04:37:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-cg1674-isoformb-dz41580-boster.html2026-03-10T04:37:44+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-purple-sea-urchin-wnt8-s-dz41588-boster.html2026-03-10T04:37:44+00:00daily0.9 https://www.bosterbio.com/products/consumables/cell-culture-plate-cs0003-boster.html2026-03-10T04:37:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0003-cell_culture_plate-1.jpgCell Culture Platehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0003-cell_culture_plate-2.jpgCell Culture Platehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0003-cell_culture_plate-3.jpgCell Culture Platehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0003-cell_culture_plate-4.jpgCell Culture Plate https://www.bosterbio.com/products/consumables/cell-culture-dish-cs0004-boster.html2026-03-10T04:37:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0004-cell_culture_dish-1.jpgCell Culture Dishhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0004-cell_culture_dish-2.jpgCell Culture Dishhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0004-cell_culture_dish-3.jpgCell Culture Dishhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0004-cell_culture_dish-4.jpgCell Culture Dish https://www.bosterbio.com/products/consumables/cell-culture-insert-cs0005-boster.html2026-03-10T04:37:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0005-cell_culture_insert-1.jpgCell Culture Inserthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0005-cell_culture_insert-2.jpgCell Culture Inserthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0005-cell_culture_insert-3.jpgCell Culture Inserthttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0005-cell_culture_insert-4.jpgCell Culture Insert https://www.bosterbio.com/products/consumables/multi-layer-cell-culture-flask-cs0007-boster.html2026-03-10T04:37:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-1.jpgMulti-layer Cell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-2.jpgMulti-layer Cell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-3.jpgMulti-layer Cell Culture Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-4.jpgMulti-layer Cell Culture Flask https://www.bosterbio.com/products/consumables/cell-culture-chamber-slides-cs0006-boster.html2026-03-10T04:37:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-1.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-2.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-3.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-4.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-5.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-6.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-7.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-8.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-9.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-10.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-11.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-12.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-13.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-14.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-15.jpgCell Culture Chamber Slideshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0006-cell-culture-chamber_slides-16.jpgCell Culture Chamber Slides https://www.bosterbio.com/catalog/product/view/id/1265692026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02111-2-pum1-primary-antibodies-wb-testing-1.jpgAnti-PUM1 Antibody Picoband® Western blot analysis of PUM1 using anti-PUM1 antibody (A02111-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human Caco-2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PUM1 antigen affinity purified polyclonal antibody (Catalog # A02111-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PUM1 at approximately 140 kDa. The expected band size for PUM1 is at 126 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02111-2-pum1-primary-antibodies-if-testing-2.jpgAnti-PUM1 Antibody Picoband® IF analysis of PUM1 using anti-PUM1 antibody (A02111-2). PUM1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-PUM1 Antibody (A02111-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02111-2-pum1-primary-antibodies-fcm-testing-3.jpgAnti-PUM1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-PUM1 antibody (A02111-2). Overlay histogram showing U251 cells stained with A02111-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PUM1 Antibody (A02111-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265702026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10537-1-naxe-primary-antibodies-wb-testing-1.jpgAnti-NAXE Antibody Picoband® Western blot analysis of NAXE using anti-NAXE antibody (A10537-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: rat heart tissue lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat liver tissue lysates, Lane 5: mouse heart tissue lysates, Lane 6: mouse kidney tissue lysates, Lane 7: mouse liver tissue lysaets. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAXE antigen affinity purified polyclonal antibody (Catalog # A10537-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAXE at approximately 26 kDa. The expected band size for NAXE is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10537-1-naxe-primary-antibodies-ihc-testing-2.jpgAnti-NAXE Antibody Picoband® IHC analysis of NAXE using anti-NAXE antibody (A10537-1). NAXE was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NAXE Antibody (A10537-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10537-1-naxe-primary-antibodies-ihc-testing-3.jpgAnti-NAXE Antibody Picoband® IHC analysis of NAXE using anti-NAXE antibody (A10537-1). NAXE was detected in a paraffin-embedded section of mouse testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NAXE Antibody (A10537-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10537-1-naxe-primary-antibodies-ihc-testing-4.jpgAnti-NAXE Antibody Picoband® IHC analysis of NAXE using anti-NAXE antibody (A10537-1). NAXE was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NAXE Antibody (A10537-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10537-1-naxe-primary-antibodies-fcm-testing-5.jpgAnti-NAXE Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NAXE antibody (A10537-1). Overlay histogram showing HEL cells stained with A10537-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NAXE Antibody (A10537-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265712026-03-17T05:16:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-wb-testing-1.jpgAnti-MATK Antibody Picoband® Western blot analysis of MATK using anti-MATK antibody (A02050-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse thymus tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MATK antigen affinity purified polyclonal antibody (Catalog # A02050-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MATK at approximately 52 kDa. The expected band size for MATK is at 56 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-ihc-testing-2.jpgAnti-MATK Antibody Picoband® IHC analysis of MATK using anti-MATK antibody (A02050-2). MATK was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATK Antibody (A02050-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-ihc-testing-3.jpgAnti-MATK Antibody Picoband® IHC analysis of MATK using anti-MATK antibody (A02050-2). MATK was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATK Antibody (A02050-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-ihc-testing-4.jpgAnti-MATK Antibody Picoband® IHC analysis of MATK using anti-MATK antibody (A02050-2). MATK was detected in a paraffin-embedded section of human teratoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATK Antibody (A02050-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-ihc-testing-5.jpgAnti-MATK Antibody Picoband® IHC analysis of MATK using anti-MATK antibody (A02050-2). MATK was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MATK Antibody (A02050-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-if-testing-6.jpgAnti-MATK Antibody Picoband® IF analysis of MATK using anti-MATK antibody (A02050-2). MATK was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MATK Antibody (A02050-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-if-testing-1.jpgAnti-MATK Antibody Picoband®IF analysis of MATK using anti-MATK antibody (A02050-2). MATK was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MATK Antibody (A02050-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02050-2-matk-primary-antibodies-fcm-testing-7.jpgAnti-MATK Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-MATK antibody (A02050-2). Overlay histogram showing Caco-2 cells stained with A02050-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MATK Antibody (A02050-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265722026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02030-1-madd-primary-antibodies-wb-testing-1.jpgAnti-MADD Antibody Picoband® Western blot analysis of MADD using anti-MADD antibody (A02030-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MADD antigen affinity purified polyclonal antibody (Catalog # A02030-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MADD at approximately 240 kDa. The expected band size for MADD is at 183 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02030-1-madd-primary-antibodies-fcm-testing-2.jpgAnti-MADD Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MADD antibody (A02030-1). Overlay histogram showing Hela cells stained with A02030-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MADD Antibody (A02030-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265732026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-wb-testing-1.jpgAnti-ATP1A2 Antibody Picoband® Western blot analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates,(100°C boiled for 5 minutes) Lane 2: rat brain tissue lysates,(37°C incubated for 10 minutes) Lane 3: mouse brain tissue lysates,(100°C boiled for 5 minutes) Lane 4: mouse brain tissue lysates.(37°C incubated for 10 minutes) After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP1A2 antigen affinity purified polyclonal antibody (Catalog # A02064-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP1A2 at approximately 112 kDa. The expected band size for ATP1A2 is at 112 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-ihc-testing-2.jpgAnti-ATP1A2 Antibody Picoband® IHC analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). ATP1A2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A2 Antibody (A02064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-ihc-testing-3.jpgAnti-ATP1A2 Antibody Picoband® IHC analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). ATP1A2 was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A2 Antibody (A02064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-ihc-testing-4.jpgAnti-ATP1A2 Antibody Picoband® IHC analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). ATP1A2 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A2 Antibody (A02064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-ihc-testing-5.jpgAnti-ATP1A2 Antibody Picoband®IHC analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). ATP1A2 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A2 Antibody (A02064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-ihc-testing-6.jpgAnti-ATP1A2 Antibody Picoband®IHC analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). ATP1A2 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A2 Antibody (A02064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-ihc-testing-7.jpgAnti-ATP1A2 Antibody Picoband®IHC analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). ATP1A2 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A2 Antibody (A02064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02064-1-atp1a2-primary-antibodies-ihc-testing-8.jpgAnti-ATP1A2 Antibody Picoband®IHC analysis of ATP1A2 using anti-ATP1A2 antibody (A02064-1). ATP1A2 was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ATP1A2 Antibody (A02064-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1265742026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02678-1-cxcl13-primary-antibodies-wb-testing-1.jpgAnti-BCA1/CXCL13 Antibody Picoband® Western blot analysis of BCA1/CXCL13 using anti-BCA1/CXCL13 antibody (A02678-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. Lane 1: recombinant human CXCL13 protein. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCA1/CXCL13 antigen affinity purified polyclonal antibody (Catalog # A02678-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCA1/CXCL13 at approximately 9 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02678-1-cxcl13-primary-antibodies-ihc-testing-2.jpgAnti-BCA1/CXCL13 Antibody Picoband® IHC analysis of BCA1/CXCL13 using anti-BCA1/CXCL13 antibody (A02678-1). BCA1/CXCL13 was detected in a paraffin-embedded section of human appendiceal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BCA1/CXCL13 Antibody (A02678-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02678-1-cxcl13-primary-antibodies-fcm-testing-3.jpgAnti-BCA1/CXCL13 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-BCA1/CXCL13 antibody (A02678-1). Overlay histogram showing SH-SY5Y cells stained with A02678-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-BCA1/CXCL13 Antibody (A02678-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265752026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-2-scd-primary-antibodies-wb-testing-1.jpgAnti-SCD Antibody Picoband® Western blot analysis of SCD using anti-SCD antibody (A00588-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCD antigen affinity purified polyclonal antibody (Catalog # A00588-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SCD at approximately 37 kDa. The expected band size for SCD is at 41 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-2-scd-primary-antibodies-if-testing-2.jpgAnti-SCD Antibody Picoband® IF analysis of SCD using anti-SCD antibody (A00588-2). SCD was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-SCD Antibody (A00588-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-2-scd-primary-antibodies-fcm-testing-3.jpgAnti-SCD Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-SCD antibody (A00588-2). Overlay histogram showing Caco-2 cells stained with A00588-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SCD Antibody (A00588-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00588-2-scd-primary-antibodies-ip-testing-4.jpgAnti-SCD Antibody Picoband® Immunoprecipitating SCD in A431 whole cell lysate. Western blot analysis of SCD using anti-SCD antibody (A00588-2). Lane 1: A431 whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-SCD antibody in A431 whole cell lysate. Lane 3: anti-SCD antibody (2μg) + A431 whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-SCD antigen affinity purified polyclonal antibody (A00588-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for SCD at approximately 37 kDa. The expected band size for SCD is at 41 kDa. https://www.bosterbio.com/catalog/product/view/id/1265762026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00517-2-col2ca1-primary-antibodies-wb-testing-1.jpgAnti-Collagen Type II/COL2A1 Antibody Picoband® Western blot analysis of Collagen Type II/COL2A1 using anti-Collagen Type II/COL2A1 antibody (A00517-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat bone tissue lysates(100°C boiled for 5 minutes), Lane 2: rat bone tissue lysates(37°C incubated for 10 minutes), Lane 3: mouse bone tissue lysates(100°C boiled for 5 minutes). After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Collagen Type II/COL2A1 antigen affinity purified polyclonal antibody (Catalog # A00517-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Collagen Type II/COL2A1 at approximately 150-180 kDa. The expected band size for Collagen Type II/COL2A1 is at 142 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00517-2-col2ca1-primary-antibodies-ihc-testing-2.jpgAnti-Collagen Type II/COL2A1 Antibody Picoband® IHC analysis of Collagen Type II/COL2A1 using anti-Collagen Type II/COL2A1 antibody (A00517-2). Collagen Type II/COL2A1 was detected in a paraffin-embedded section of mouse knee cartilage tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Collagen Type II/COL2A1 Antibody (A00517-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00517-2-col2ca1-primary-antibodies-ihc-testing-3.jpgAnti-Collagen Type II/COL2A1 Antibody Picoband® IHC analysis of Collagen Type II/COL2A1 using anti-Collagen Type II/COL2A1 antibody (A00517-2). Collagen Type II/COL2A1 was detected in a paraffin-embedded section of rat knee cartilage tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Collagen Type II/COL2A1 Antibody (A00517-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1265772026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12287-1-hddc3-primary-antibodies-wb-testing-1.jpgAnti-HDDC3 Antibody Picoband® Western blot analysis of HDDC3 using anti-HDDC3 antibody (A12287-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HDDC3 antigen affinity purified polyclonal antibody (Catalog # A12287-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HDDC3 at approximately 22 kDa. The expected band size for HDDC3 is at 20 kDa. https://www.bosterbio.com/catalog/product/view/id/1265782026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00142-2-bcl6-primary-antibodies-wb-testing-1.jpgAnti-BCL6 Antibody Picoband® Western blot analysis of BCL6 using anti-BCL6 antibody (A00142-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human Daudi whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCL6 antigen affinity purified polyclonal antibody (Catalog # A00142-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCL6 at approximately 88 kDa. The expected band size for BCL6 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00142-2-bcl6-primary-antibodies-fcm-testing-2.jpgAnti-BCL6 Antibody Picoband® Flow Cytometry analysis of Raji cells using anti-BCL6 antibody (A00142-2). Overlay histogram showing Raji cells stained with A00142-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BCL6 Antibody (A00142-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265792026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16079-3-mob3abc-primary-antibodies-wb-testing-1.jpgAnti-MOB3A/B/C Antibody Picoband® Western blot analysis of MOB3A/B/C using anti-MOB3A/B/C antibody (A16079-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Raji whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat thymus tissue lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MOB3A/B/C antigen affinity purified polyclonal antibody (Catalog # A16079-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MOB3A/B/C at approximately 25 kDa. The expected band size for MOB3A/B/C is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16079-3-mob3abc-primary-antibodies-fcm-testing-2.jpgAnti-MOB3A/B/C Antibody Picoband® Flow Cytometry analysis of Raji cells using anti-MOB3A/B/C antibody (A16079-3). Overlay histogram showing Raji cells stained with A16079-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MOB3A/B/C Antibody (A16079-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265802026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02465-2-mvk-primary-antibodies-wb-testing-1.jpgAnti-MVK Antibody Picoband®Western blot analysis of MVK using anti-MVK antibody (A02465-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates, Lane 5: rat RH35 whole cell lysates, Lane 6: mouse HEPA1/6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MVK antigen affinity purified polyclonal antibody (A02465-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MVK at approximately 42 kDa. The expected band size for MVK is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02465-2-mvk-primary-antibodies-ihc-testing-1.jpgAnti-MVK Antibody Picoband®IHC analysis of MVK using anti-MVK antibody (A02465-2). MVK was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MVK Antibody (A02465-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02465-2-mvk-primary-antibodies-ihc-testing-2.jpgAnti-MVK Antibody Picoband®IHC analysis of MVK using anti-MVK antibody (A02465-2). MVK was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MVK Antibody (A02465-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02465-2-mvk-primary-antibodies-if-testing-1.jpgAnti-MVK Antibody Picoband®IF analysis of MVK using anti-MVK antibody (A02465-2). MVK was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-MVK Antibody (A02465-2) overnight at 4°C. Cy3 Conjugated Goat Anti-Rabbit IgG (BA1032) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02465-2-mvk-primary-antibodies-ip-testing-1.jpgAnti-MVK Antibody Picoband®Immunoprecipitating (IP) MVK in HepG2 whole cell lysate. Western blot analysis of MVK using anti-MVK antibody (A02465-2); Lane 1: HepG2 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-MVK antibody in HepG2 whole cell lysate; Lane 3: anti-MVK antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MVK antigen affinity purified polyclonal antibody (A02465-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for MVK at approximately 42 kDa. The expected band size for MVK is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02465-2-mvk-primary-antibodies-fcm-testing-1.jpgAnti-MVK Antibody Picoband®Flow Cytometry analysis of HepG2 cells using anti-MVK antibody (A02465-2). Overlay histogram showing HepG2 cells stained with A02465-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MVK Antibody (A02465-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265812026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06546-1-lsm14a-primary-antibodies-wb-testing-1.jpgAnti-LSM14A Antibody Picoband® Western blot analysis of LSM14A using anti-LSM14A antibody (A06546-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates, Lane 4: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LSM14A antigen affinity purified polyclonal antibody (Catalog # A06546-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LSM14A at approximately 60 kDa. The expected band size for LSM14A is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06546-1-lsm14a-primary-antibodies-if-testing-2.jpgAnti-LSM14A Antibody Picoband® IF analysis of LSM14A using anti-LSM14A antibody (A06546-1). LSM14A was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LSM14A Antibody (A06546-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06546-1-lsm14a-primary-antibodies-fcm-testing-3.jpgAnti-LSM14A Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-LSM14A antibody (A06546-1). Overlay histogram showing SH-SY5Y cells stained with A06546-1(Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LSM14A Antibody (A06546-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06546-1-lsm14a-primary-antibodies-ip-testing-4.jpgAnti-LSM14A Antibody Picoband® Immunoprecipitating LSM14A in A549 whole cell lysate . Western blot analysis of LSM14A using anti-LSM14A antibody (A06546-1). Lane 1: A549 whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-LSM14A antibody in A549 whole cell lysate. Lane 3: anti-LSM14A antibody (2μg) + A549 whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-LSM14A antigen affinity purified polyclonal antibody (A06546-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for LSM14A at approximately 60 kDa. The expected band size for LSM14A is at 51 kDa. https://www.bosterbio.com/catalog/product/view/id/1265822026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09668-2-ganab-primary-antibodies-wb-testing-1.jpgAnti-GANAB Antibody Picoband® Western blot analysis of GANAB using anti-GANAB antibody (A09668-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GANAB antigen affinity purified polyclonal antibody (Catalog # A09668-2) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GANAB at approximately 100 kDa. The expected band size for GANAB is at 107 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09668-2-ganab-primary-antibodies-ihc-testing-2.jpgAnti-GANAB Antibody Picoband® IHC analysis of GANAB using anti-GANAB antibody (A09668-2). GANAB was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GANAB Antibody (A09668-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09668-2-ganab-primary-antibodies-if-testing-3.jpgAnti-GANAB Antibody Picoband® IF analysis of GANAB using anti-GANAB antibody (A09668-2). GANAB was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GANAB Antibody (A09668-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09668-2-ganab-primary-antibodies-if-testing-4.jpgAnti-GANAB Antibody Picoband® IF analysis of GANAB using anti-GANAB antibody (A09668-2). GANAB was detected in a paraffin-embedded section of human placenta tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-GANAB Antibody (A09668-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09668-2-ganab-primary-antibodies-fcm-testing-5.jpgAnti-GANAB Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-GANAB antibody (A09668-2). Overlay histogram showing SH-SY5Y cells stained with A09668-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GANAB Antibody (A09668-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265832026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10999-1-scnm1-primary-antibodies-wb-testing-1.jpgAnti-SCNM1 Antibody Picoband® Western blot analysis of SCNM1 using anti-SCNM1 antibody (A10999-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: rat lung tissue lysates, Lane 3: rat stomach tissue lysates, Lane 4: mouse lung tissue lysates, Lane 5: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SCNM1 antigen affinity purified polyclonal antibody (Catalog # A10999-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SCNM1 at approximately 26 kDa. The expected band size for SCNM1 is at 26 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10999-1-scnm1-primary-antibodies-ihc-testing-2.jpgAnti-SCNM1 Antibody Picoband® IHC analysis of SCNM1 using anti-SCNM1 antibody (A10999-1). SCNM1 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCNM1 Antibody (A10999-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10999-1-scnm1-primary-antibodies-ihc-testing-3.jpgAnti-SCNM1 Antibody Picoband® IHC analysis of SCNM1 using anti-SCNM1 antibody (A10999-1). SCNM1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCNM1 Antibody (A10999-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10999-1-scnm1-primary-antibodies-ihc-testing-4.jpgAnti-SCNM1 Antibody Picoband® IHC analysis of SCNM1 using anti-SCNM1 antibody (A10999-1). SCNM1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SCNM1 Antibody (A10999-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10999-1-scnm1-primary-antibodies-fcm-testing-5.jpgAnti-SCNM1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-SCNM1 antibody (A10999-1). Overlay histogram showing U251 cells stained with A10999-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SCNM1 Antibody (A10999-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265842026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05714-1-marveld2-primary-antibodies-wb-testing-1.jpgAnti-MARVELD2 Antibody Picoband® Western blot analysis of MARVELD2 using anti-MARVELD2 antibody (A05714-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MARVELD2 antigen affinity purified polyclonal antibody (Catalog # A05714-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MARVELD2 at approximately 64 kDa. The expected band size for MARVELD2 is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05714-1-marveld2-primary-antibodies-wb-testing-2.jpgAnti-MARVELD2 Antibody Picoband® Western blot analysis of MARVELD2 using anti-MARVELD2 antibody (A05714-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat small intestine tissue lysates, Lane 2: rat kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MARVELD2 antigen affinity purified polyclonal antibody (Catalog # A05714-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MARVELD2 at approximately 64 kDa. The expected band size for MARVELD2 is at 64 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05714-1-marveld2-primary-antibodies-ihc-testing-3.jpgAnti-MARVELD2 Antibody Picoband® IHC analysis of MARVELD2 using anti-MARVELD2 antibody (A05714-1). MARVELD2 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MARVELD2 Antibody (A05714-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05714-1-marveld2-primary-antibodies-fcm-testing-4.jpgAnti-MARVELD2 Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-MARVELD2 antibody (A05714-1). Overlay histogram showing Caco-2 cells stained with A05714-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MARVELD2 Antibody (A05714-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265852026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15360-1-mettl15-primary-antibodies-wb-testing-1.jpgAnti-METT5D1/METTL15 Antibody Picoband® Western blot analysis of METT5D1/METTL15 using anti-METT5D1/METTL15 antibody (A15360-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates, Lane 7: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-METT5D1/METTL15 antigen affinity purified polyclonal antibody (Catalog # A15360-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for METT5D1/METTL15 at approximately 46 kDa. The expected band size for METT5D1/METTL15 is at 46 kDa. https://www.bosterbio.com/catalog/product/view/id/1265892026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04546-2-magi2-primary-antibodies-wb-testing-1.jpgAnti-MAGI2 Antibody Picoband® Western blot analysis of MAGI2 using anti-MAGI2 antibody (A04546-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAGI2 antigen affinity purified polyclonal antibody (Catalog # A04546-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MAGI2 at approximately 140 kDa. The expected band size for MAGI2 is at 159 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04546-2-magi2-primary-antibodies-fcm-testing-2.jpgAnti-MAGI2 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-MAGI2 antibody (A04546-2). Overlay histogram showing SH-SY5Y cells stained with A04546-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MAGI2 Antibody (A04546-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265912026-03-17T05:16:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-wb-testing-1.jpgAnti-GBF1 Antibody Picoband® Western blot analysis of GBF1 using anti-GBF1 antibody (A01817-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GBF1 antigen affinity purified polyclonal antibody (Catalog # A01817-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GBF1 at approximately 250 kDa. The expected band size for GBF1 is at 207 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-wb-testing-2.jpgAnti-GBF1 Antibody Picoband® Western blot analysis of GBF1 using anti-GBF1 antibody (A01817-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human CACO-2 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GBF1 antigen affinity purified polyclonal antibody (A01817-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GBF1 at approximately 250 kDa. The expected band size for GBF1 is at 207 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-ihc-testing-3.jpgAnti-GBF1 Antibody Picoband® IHC analysis of GBF1 using anti-GBF1 antibody (A01817-1). GBF1 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GBF1 Antibody (A01817-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-ihc-testing-4.jpgAnti-GBF1 Antibody Picoband® IHC analysis of GBF1 using anti-GBF1 antibody (A01817-1). GBF1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GBF1 Antibody (A01817-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-ihc-testing-5.jpgAnti-GBF1 Antibody Picoband® IHC analysis of GBF1 using anti-GBF1 antibody (A01817-1). GBF1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GBF1 Antibody (A01817-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-ihc-testing-6.jpgAnti-GBF1 Antibody Picoband® IHC analysis of GBF1 using anti-GBF1 antibody (A01817-1). GBF1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GBF1 Antibody (A01817-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-if-testing-7.jpgAnti-GBF1 Antibody Picoband® IF analysis of GBF1 using anti-GBF1 antibody (A01817-1). GBF1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GBF1 Antibody (A01817-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01817-1-gbf1-primary-antibodies-fcm-testing-8.jpgAnti-GBF1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GBF1 antibody (A01817-1). Overlay histogram showing HepG2 cells stained with A01817-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GBF1 Antibody (A01817-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265922026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03067-1-gbp1-primary-antibodies-wb-testing-1.jpgAnti-GBP1 Antibody Picoband® Western blot analysis of GBP1 using anti-GBP1 antibody (A03067-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates, Lane 2: human HUVEC whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat spleen tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse spleen tissue lysayes. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GBP1 antigen affinity purified polyclonal antibody (Catalog # A03067-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GBP1 at approximately 68 kDa. The expected band size for GBP1 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03067-1-gbp1-primary-antibodies-ihc-testing-2.jpgAnti-GBP1 Antibody Picoband® IHC analysis of GBP1 using anti-GBP1 antibody (A03067-1). GBP1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GBP1 Antibody (A03067-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03067-1-gbp1-primary-antibodies-ihc-testing-3.jpgAnti-GBP1 Antibody Picoband® IHC analysis of GBP1 using anti-GBP1 antibody (A03067-1). GBP1 was detected in a paraffin-embedded section of mouse heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GBP1 Antibody (A03067-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03067-1-gbp1-primary-antibodies-ihc-testing-4.jpgAnti-GBP1 Antibody Picoband® IHC analysis of GBP1 using anti-GBP1 antibody (A03067-1). GBP1 was detected in a paraffin-embedded section of rat heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GBP1 Antibody (A03067-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03067-1-gbp1-primary-antibodies-if-testing-5.jpgAnti-GBP1 Antibody Picoband® IF analysis of GBP1 using anti-GBP1 antibody (A03067-1). GBP1 was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GBP1 Antibody (A03067-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03067-1-gbp1-primary-antibodies-ip-testing-6.jpgAnti-GBP1 Antibody Picoband® Immunoprecipitating GBP1 in Hela whole cell lysate. Western blot analysis of GBP1 using anti-GBP1 antibody (A03067-1). Lane 1: Hela whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-GBP1 antibody in Hela whole cell lysate. Lane 3: anti-GBP1 antibody (2μg) + Hela whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-GBP1 antigen affinity purified polyclonal antibody (A03067-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for GBP1 at approximately 68 kDa. The expected band size for GBP1 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03067-1-gbp1-primary-antibodies-fcm-testing-7.jpgAnti-GBP1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-GBP1 antibody (A03067-1). Overlay histogram showing MCF-7 cells stained with A03067-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-GBP1 Antibody (A03067-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1265962026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04173-abce1-primary-antibodies-wb-testing-1.jpgAnti-ABCE1 Antibody Picoband® Western blot analysis of ABCE1 using anti-ABCE1 antibody (A04173). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human U20S whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse 4T1 whole cell lysates, Laen 8: mouse NIH/3T3 whole cell lysate. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCE1 antigen affinity purified polyclonal antibody (Catalog # A04173) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ABCE1 at approximately 67 kDa. The expected band size for ABCE1 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04173-abce1-primary-antibodies-ihc-testing-4.jpgAnti-ABCE1 Antibody Picoband®IHC analysis of ABCE1 using anti-ABCE1 antibody (A04173). ABCE1 was detected in a paraffin-embedded section of human testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCE1 Antibody (A04173) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04173-abce1-primary-antibodies-ihc-testing-2.jpgAnti-ABCE1 Antibody Picoband® IHC analysis of ABCE1 using anti-ABCE1 antibody (A04173). ABCE1 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCE1 Antibody (A04173) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04173-abce1-primary-antibodies-ihc-testing-3.jpgAnti-ABCE1 Antibody Picoband® IHC analysis of ABCE1 using anti-ABCE1 antibody (A04173). ABCE1 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABCE1 Antibody (A04173) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04173-abce1-primary-antibodies-if-testing-4.jpgAnti-ABCE1 Antibody Picoband® IF analysis of ABCE1 using anti-ABCE1 antibody (A04173). ABCE1 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ABCE1 Antibody (A04173) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04173-abce1-primary-antibodies-fcm-testing-5.jpgAnti-ABCE1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-ABCE1 antibody (A04173). Overlay histogram showing U251 cells stained with A04173 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABCE1 Antibody (A04173, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04173-abce1-primary-antibodies-wb-testing-6.jpgAnti-ABCE1 Antibody Picoband® Western blot analysis of ABCE1 using anti-ABCE1 antibody (A04173). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human U20S whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: mouse 4T1 whole cell lysates, Lane 5: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABCE1 antigen affinity purified polyclonal antibody (A04173) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for ABCE1 at approximately 67 kDa. The expected band size for ABCE1 is at 67 kDa. https://www.bosterbio.com/catalog/product/view/id/1265992026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03990-2-maml1-primary-antibodies-wb-testing-1_1.jpgAnti-MAML1 Antibody Picoband®Western blot analysis of MAML1 using anti-MAML1 antibody (A03990-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human MOLT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MAML1 antigen affinity purified polyclonal antibody (Catalog # A03990-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MAML1 at approximately 130 kDa. The expected band size for MAML1 is at 108 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03990-2-maml1-primary-antibodies-if-testing-1.jpgAnti-MAML1 Antibody Picoband®IF analysis of MAML1 using anti-MAML1 antibody (A03990-2) and anti-Alpha Tubulin antibody (M03989-3). MAML1 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MAML1 Antibody (A03990-2) and mouse anti-Alpha Tubulin antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03990-2-maml1-primary-antibodies-fcm-testing-1.jpgAnti-MAML1 Antibody Picoband®Flow Cytometry analysis of Jurkat cells using anti-MAML1 antibody (A03990-2). Overlay histogram showing Jurkat cells stained with A03990-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MAML1 Antibody (A03990-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266012026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12284-2-ncln-primary-antibodies-wb-testing-1.jpgAnti-NCLN Antibody Picoband® Western blot analysis of NCLN using anti-NCLN antibody (A12284-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human CCRF-CEM whole cell lysates, Lane 2: human HUH-7 whole cell lysates, Lane 3: rat skeletal muscle tissue lysates, Lane 4: rat L6 whole cell lysates, Lane 5: mouse pancreas tissue lysates, Lane 6: mouse skeletal muscle tissue lysates, Lane 7: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NCLN antigen affinity purified polyclonal antibody (Catalog # A12284-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NCLN at approximately 63 kDa. The expected band size for NCLN is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12284-2-ncln-primary-antibodies-ihc-testing-2.jpgAnti-NCLN Antibody Picoband® IHC analysis of NCLN using anti-NCLN antibody (A12284-2). NCLN was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCLN Antibody (A12284-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12284-2-ncln-primary-antibodies-if-testing-3.jpgAnti-NCLN Antibody Picoband® IF analysis of NCLN using anti-NCLN antibody (A12284-2). NCLN was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NCLN Antibody (A12284-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12284-2-ncln-primary-antibodies-fcm-testing-4.jpgAnti-NCLN Antibody Picoband® Flow Cytometry analysis of JK cells using anti-NCLN antibody (A12284-2). Overlay histogram showing JK cells stained with A12284-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NCLN Antibody (A12284-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266022026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08935-1-ngef-primary-antibodies-wb-testing-1.jpgAnti-NGEF Antibody Picoband® Western blot analysis of NGEF using anti-NGEF antibody (A08935-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NGEF antigen affinity purified polyclonal antibody (Catalog # A08935-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NGEF at approximately 71 kDa. The expected band size for NGEF is at 82,71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08935-1-ngef-primary-antibodies-fcm-testing-2.jpgAnti-NGEF Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-NGEF antibody (A08935-1). Overlay histogram showing HepG2 cells stained with A08935-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NGEF Antibody (A08935-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266032026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05288-1-mtch2-primary-antibodies-wb-testing-1.jpgAnti-MTCH2 Antibody Picoband® Western blot analysis of MTCH2 using anti-MTCH2 antibody (A05288-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MTCH2 antigen affinity purified polyclonal antibody (Catalog # A05288-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MTCH2 at approximately 33 kDa. The expected band size for MTCH2 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05288-1-mtch2-primary-antibodies-ihc-testing-2.jpgAnti-MTCH2 Antibody Picoband® IHC analysis of MTCH2 using anti-MTCH2 antibody (A05288-1). MTCH2 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTCH2 Antibody (A05288-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05288-1-mtch2-primary-antibodies-ihc-testing-3.jpgAnti-MTCH2 Antibody Picoband® IHC analysis of MTCH2 using anti-MTCH2 antibody (A05288-1). MTCH2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTCH2 Antibody (A05288-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05288-1-mtch2-primary-antibodies-ihc-testing-4.jpgAnti-MTCH2 Antibody Picoband® IHC analysis of MTCH2 using anti-MTCH2 antibody (A05288-1). MTCH2 was detected in a paraffin-embedded section of rat testis tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MTCH2 Antibody (A05288-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05288-1-mtch2-primary-antibodies-if-testing-5.jpgAnti-MTCH2 Antibody Picoband® IF analysis of MTCH2 using anti-MTCH2 antibody (A05288-1). MTCH2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MTCH2 Antibody (A05288-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05288-1-mtch2-primary-antibodies-ip-testing-6.jpgAnti-MTCH2 Antibody Picoband® Immunoprecipitating MTCH2 in Hela whole cell lysate. Western blot analysis of MTCH2 using anti-MTCH2 antibody (A05288-1). Lane 1: Hela whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-MTCH2 antibody in Hela whole cell lysate. Lane 3: anti-MTCH2 antibody (2μg) + Hela whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MTCH2 antigen affinity purified polyclonal antibody (A05288-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for MTCH2 at approximately 33 kDa. The expected band size for MTCH2 is at 33 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05288-1-mtch2-primary-antibodies-fcm-testing-7.jpgAnti-MTCH2 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-MTCH2 antibody (A05288-1). Overlay histogram showing PC-3 cells stained with A05288-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MTCH2 Antibody (A05288-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266042026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18908-1-lix1l-primary-antibodies-wb-testing-1.jpgAnti-LIX1L Antibody Picoband® Western blot analysis of LIX1L using anti-LIX1L antibody (A18908-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human SiHa whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIX1L antigen affinity purified polyclonal antibody (Catalog # A18908-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIX1L at approximately 37 kDa. The expected band size for LIX1L is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18908-1-lix1l-primary-antibodies-wb-testing-2.jpgAnti-LIX1L Antibody Picoband® Western blot analysis of LIX1L using anti-LIX1L antibody (A18908-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skeletal muscle tissue lysates, Lane 2: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LIX1L antigen affinity purified polyclonal antibody (Catalog # A18908-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LIX1L at approximately 37 kDa. The expected band size for LIX1L is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18908-1-lix1l-primary-antibodies-fcm-testing-3.jpgAnti-LIX1L Antibody Picoband® Flow Cytometry analysis of JK cells using anti-LIX1L antibody (A18908-1). Overlay histogram showing JK cells stained with A18908-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LIX1L Antibody (A18908-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266052026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04819-3-nlrp2-primary-antibodies-wb-testing-1.jpgAnti-NLRP2 Antibody Picoband® Western blot analysis of NLRP2 using anti-NLRP2 antibody (A04819-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NLRP2 antigen affinity purified polyclonal antibody (Catalog # A04819-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NLRP2 at approximately 121 kDa. The expected band size for NLRP2 is at 121 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04819-3-nlrp2-primary-antibodies-if-testing-2.jpgAnti-NLRP2 Antibody Picoband® IF analysis of NLRP2 using anti-NLRP2 antibody (A04819-3). NLRP2 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NLRP2 Antibody (A04819-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04819-3-nlrp2-primary-antibodies-fcm-testing-3.jpgAnti-NLRP2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NLRP2 antibody (A04819-3). Overlay histogram showing HEL cells stained with A04819-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NLRP2 Antibody (A04819-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04819-3-nlrp2-primary-antibodies-ip-testing-4.jpgAnti-NLRP2 Antibody Picoband® Immunoprecipitating NLRP2 in A431 whole cell lysate. Western blot analysis of NLRP2 using anti-NLRP2 antibody (A04819-3). Lane 1: A431 whole cell lysates (30ug) Lane 2: Rabbit control IgG instead of anti-NLRP2 antibody in A431 whole cell lysate. Lane 3: anti-NLRP2 antibody (2μg) + A431 whole cell lysate (500μg) After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-NLRP2 antigen affinity purified polyclonal antibody (A04819-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for NLRP2 at approximately 121 kDa. The expected band size for NLRP2 is at 121 kDa. https://www.bosterbio.com/catalog/product/view/id/1266072026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04927-1-atp6v1b2-primary-antibodies-wb-testing-1.jpgAnti-ATP6V1B2 Antibody Picoband® Western blot analysis of ATP6V1B2 using anti-ATP6V1B2 antibody (A04927-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat H9C2(2-1) whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP6V1B2 antigen affinity purified polyclonal antibody (Catalog # A04927-1) at 0.25 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP6V1B2 at approximately 57 kDa. The expected band size for ATP6V1B2 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04927-1-atp6v1b2-primary-antibodies-wb-testing-2.jpgAnti-ATP6V1B2 Antibody Picoband® Western blot analysis of ATP6V1B2 using anti-ATP6V1B2 antibody (A04927-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP6V1B2 antigen affinity purified polyclonal antibody (A04927-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-DyLight 647 Conjugated secondary antibody at a dilution of 1:2000 for 1.5 hour at RT. A specific band was detected for ATP6V1B2 at approximately 57 kDa. The expected band size for ATP6V1B2 is at 57 kDa. https://www.bosterbio.com/catalog/product/view/id/1266082026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07806-3-lzts2-primary-antibodies-wb-testing-1.jpgAnti-LZTS2 Antibody Picoband® Western blot analysis of LZTS2 using anti-LZTS2 antibody (A07806-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse RM-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LZTS2 antigen affinity purified polyclonal antibody (Catalog # A07806-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LZTS2 at approximately 73-75 kDa. The expected band size for LZTS2 is at 73 kDahttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07806-3-lzts2-primary-antibodies-if-testing-2.jpgAnti-LZTS2 Antibody Picoband® IF analysis of LZTS2 using anti-LZTS2 antibody (A07806-3). LZTS2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-LZTS2 Antibody (A07806-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07806-3-lzts2-primary-antibodies-fcm-testing-3.jpgAnti-LZTS2 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-LZTS2 antibody (A07806-3). Overlay histogram showing Hela cells stained with A07806-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LZTS2 Antibody (A07806-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266092026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01475-3-rps6kb1-primary-antibodies-wb-testing-1.jpgAnti-p70 S6K/RPS6KB1 Antibody Picoband® Western blot analysis of P70 S6K/RPS6KB1 using anti-P70 S6K/RPS6KB1 antibody (A01475-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human U251 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-P70 S6K/RPS6KB1 antigen affinity purified polyclonal antibody (Catalog # A01475-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for P70 S6K/RPS6KB1 at approximately 68 kDa. The expected band size for P70 S6K/RPS6KB1 is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01475-3-rps6kb1-primary-antibodies-fcm-testing-2.jpgAnti-p70 S6K/RPS6KB1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-P70 S6K/RPS6KB1 antibody (A01475-3). Overlay histogram showing U251 cells stained with A01475-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-P70 S6K/RPS6KB1 Antibody (A01475-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266112026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01719-abr-primary-antibodies-wb-testing-1.jpgAnti-ABR Antibody Picoband® Western blot analysis of ABR using anti-ABR antibody (A01719). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ABR antigen affinity purified polyclonal antibody (Catalog # A01719) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ABR at approximately 100 kDa. The expected band size for ABR is at 98 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01719-abr-primary-antibodies-ihc-testing-2.jpgAnti-ABR Antibody Picoband® IHC analysis of ABR using anti-ABR antibody (A01719). ABR was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABR Antibody (A01719) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01719-abr-primary-antibodies-ihc-testing-3.jpgAnti-ABR Antibody Picoband® IHC analysis of ABR using anti-ABR antibody (A01719). ABR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABR Antibody (A01719) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01719-abr-primary-antibodies-ihc-testing-4.jpgAnti-ABR Antibody Picoband® IHC analysis of ABR using anti-ABR antibody (A01719). ABR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ABR Antibody (A01719) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01719-abr-primary-antibodies-if-testing-5.jpgAnti-ABR Antibody Picoband® IF analysis of ABR using anti-ABR antibody (A01719). ABR was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ABR Antibody (A01719) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01719-abr-primary-antibodies-fcm-testing-6.jpgAnti-ABR Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-ABR antibody (A01719). Overlay histogram showing 293T cells stained with A01719 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ABR Antibody (A01719, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266142026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11598-1-galnt15-primary-antibodies-wb-testing-1.jpgAnti-GALNT15 Antibody Picoband® Western blot analysis of GALNT15 using anti-GALNT15 antibody (A11598-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: rat spleen tissue lysates, Lane 3: rat ovary tissue lysates, Lane 4: mouse spleen tissue lysates, Lane 5: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALNT15 antigen affinity purified polyclonal antibody (Catalog # A11598-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GALNT15 at approximately 73 kDa. The expected band size for GALNT15 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11598-1-galnt15-primary-antibodies-wb-testing-2.jpgAnti-GALNT15 Antibody Picoband® Western blot analysis of GALNT15 using anti-GALNT15 antibody (A11598-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GALNT15 antigen affinity purified polyclonal antibody (A11598-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GALNT15 at approximately 73 kDa. The expected band size for GALNT15 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11598-1-galnt15-primary-antibodies-if-testing-3.jpgAnti-GALNT15 Antibody Picoband® IF analysis of GALNT15 using anti-GALNT15 antibody (A11598-1). GALNT15 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-GALNT15 Antibody (A11598-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11598-1-galnt15-primary-antibodies-fcm-testing-4.jpgAnti-GALNT15 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-GALNT15 antibody (A11598-1). Overlay histogram showing 293T cells stained with A11598-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GALNT15 Antibody (A11598-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1266202026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01896-2-ccr1-primary-antibodies-wb-testing-1.jpgAnti-CCR1 Antibody Picoband® Western blot analysis of CCR1 using anti-CCR1 antibody (A01896-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CCR1 antigen affinity purified polyclonal antibody (Catalog # A01896-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CCR1 at approximatel 41 kDa. The expected band size for CCR1 is at 41 kDa. https://www.bosterbio.com/catalog/product/view/id/1266212026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02456-1-slc22a6-primary-antibodies-wb-testing-1.jpgAnti-OAT1/SLC22A6 Antibody Picoband® Western blot analysis of OAT1/SLC22A6 using anti-OAT1/SLC22A6 antibody (A02456-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human placenta tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OAT1/SLC22A6 antigen affinity purified polyclonal antibody (Catalog # A02456-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OAT1/SLC22A6 at approximately 70 kDa. The expected band size for OAT1/SLC22A6 is at 62 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02456-1-slc22a6-primary-antibodies-fcm-testing-2.jpgAnti-OAT1/SLC22A6 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-OAT1/SLC22A6 antibody (A02456-1). Overlay histogram showing THP-1 cells stained with A02456-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-OAT1/SLC22A6 Antibody (A02456-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/products/consumables/biofactory-cs0008-boster.html2026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-1_1.jpgBioFactoryhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-2_1.jpgBioFactoryhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-3_1.jpgBioFactoryhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0007-multi-layer_cell-culture-flasks-4_1.jpgBioFactory https://www.bosterbio.com/products/consumables/bioprocess-systems-accessorie-cs0009-boster.html2026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0009-bioprocess-systems-accessorie-1.jpgBioprocess Systems Accessoriehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0009-bioprocess-systems-accessorie-2.jpgBioprocess Systems Accessorie https://www.bosterbio.com/products/consumables/erlenmeyer-flasks-accessories-cs0010-boster.html2026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0010-erlenmeyer-flask-accessories-1.jpgErlenmeyer Flask Accessorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0010-erlenmeyer-flask-accessories-2.jpgErlenmeyer Flask Accessories https://www.bosterbio.com/products/consumables/erlenmeyer-flask-cs0011-boster.html2026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-1_1.jpgErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-2_1.jpgErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-3_1.jpgErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-4.jpgErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-5_1.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-6.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-7.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-8.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-9.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-10.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-11.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-12.pngErlenmeyer Flaskhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0011-erlenmeyer-flask-13.jpgErlenmeyer Flask https://www.bosterbio.com/products/consumables/2-3-5l-erlenmeyer-flask-cs0012-boster.html2026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-1.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-2.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-3.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-4.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-5.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-6.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-7.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-8.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-9.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-10.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-11.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-12.jpg2L/3L/5L Erlenmeyer Flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0012-2l3l5l-erlenmeyer-flasks-13.jpg2L/3L/5L Erlenmeyer Flasks https://www.bosterbio.com/products/consumables/2-3-5l-erlenmeyer-flask-accesories-cs0013-boster.html2026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-1.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-2.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-3.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-4.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-5.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-6.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-7.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-8.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-9.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-10.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-11.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-12.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-13.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-14.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-15.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-16.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-17.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-18.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-19.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-20.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-21.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-22.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-23.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-24.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-25.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-26.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-27.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-28.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-29.jpg2L/3L/5L Erlenmeyer Flask Accesorieshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-30.jpg2L/3L/5L Erlenmeyer Flask Accesories https://www.bosterbio.com/products/consumables/closed-systems-for-erlenmeyer-flasks-with-flasks-cs0014-boster.html2026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-1_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-2_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-3_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-4_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-5_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-6_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-7_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-8_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-9_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-10_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-11_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-12_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-13_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-14_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-15_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-16_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-17_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-18_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-19_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-20_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-21_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-22_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-23_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-24_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-25_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-26_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-27_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-28_1.jpgClosed Systems for Erlenmeyer Flasks, with flaskshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0013-2l3l5l-erlenmeyer-flask-accesories-29_1.jpgClosed Systems for Erlenmeyer Flasks, with flasks https://www.bosterbio.com/catalog/product/view/id/1266292026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp00973-1.jpgHuman recombinant OAS1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266302026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41218-1.jpgHuman recombinant MNDA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266312026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq13630-1.jpgHuman recombinant TSTA3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266322026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9y2v2-1.jpgHuman recombinant CARHSP1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266332026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9y3d8-1.jpgHuman recombinant TAF9 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266342026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq10589-1.jpgHuman recombinant BST-2/Tetherin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266352026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9bzg1-1.jpgHuman recombinant RAB34 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266362026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto96007-1.jpgHuman recombinant MOCS2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266372026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp20231-2.jpgHuman recombinant Tryptase beta-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266382026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota0a0b4j2f8.jpgHuman recombinant RNA polymerase II subunit RPB11-b2/POLR2J3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266392026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16410-3.jpgHuman recombinant CTLA4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266402026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto15304-1.jpgHuman recombinant SIVA1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266412026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp0c7q2-1.jpgHuman recombinant ARSM2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266422026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01911-1.jpgHuman recombinant HLA-DRB1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266432026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq63hm9-1.jpgHuman recombinant PLCXD3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266442026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq16385-2.jpgHuman recombinant SSX2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266452026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9byz8-2.jpgHuman recombinant Reg4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266462026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto00253-1.jpgHuman recombinant AgRP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266472026-03-10T04:37:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq16620-1.jpgHuman recombinant TrkB protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266482026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6qlq4.jpgMouse recombinant Dectin-1/CLEC7A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266492026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16278-1.jpgHuman recombinant beta -Galactosidase-1/GLB1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266502026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8nbl1-2.jpgHuman recombinant Protein O-glucosyltransferase 1/POGLUT1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266512026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp04921-1.jpgHuman recombinant Glycophorin C/GYPC protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266522026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10721-1.jpgHuman recombinant CD117/c-kit protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266532026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq08345-1.jpgHuman recombinant DDR1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266542026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15813-1.jpgHuman recombinant CD1d protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266552026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp43489-1.jpgHuman recombinant OX40/TNFRSF4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266562026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq495a1-1.jpgHuman recombinant TIGIT protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266572026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq04900-1.jpgHuman recombinant CD164 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266582026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq7z6a9-1.jpgHuman recombinant BTLA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266592026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09619-1.jpgHuman recombinant PDGF R beta protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266602026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp27930-1.jpgHuman recombinant IL-1R beta/IL1R2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266612026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9ubk5-1.jpgHuman recombinant DAP10/HCST protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266622026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16144-1.jpgHuman recombinant Integrin beta 4/CD104 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266632026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16671-1.jpgHuman recombinant CD36/SR-B3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266642026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto14786-1.jpgHuman recombinant Neuropilin 1/NRP1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266652026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq01344-1.jpgHuman recombinant IL-5R alpha/IL5RA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266662026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16070-1.jpgHuman recombinant CD44 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266672026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15391-1.jpgHuman recombinant CD19 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266682026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp53779-1.jpgHuman recombinant JNK3/MAPK10 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266692026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq10472-1.jpgHuman recombinant GalNAc Transferase 1/GALNT1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266702026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9bxj0-1.jpgHuman recombinant CTRP5/C1qTNF5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266712026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp23141-1.jpgHuman recombinant Carboxylesterase 1/CES1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266722026-03-10T04:37:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp42081-1.jpgHuman recombinant B7-2/CD86 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266732026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq04771-1-sds-page.jpgHuman recombinant Activin RIA/ALK-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266742026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp56817-1-sds-page.jpgHuman recombinant BACE-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266752026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9hbe4-4-sds-page.jpgHuman recombinant Animal Free IL-21 Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266762026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp32942-1-sds-page.jpgHuman recombinant ICAM-3/CD50 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266772026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01582-5-sds-page.jpgMouse recombinant IL-1 alpha/IL1A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266782026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9bvh7-sds-page.jpgHuman recombinant ST6GALNAC5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266792026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp18510-4-sds-page.jpgHuman recombinant IL-1Ra/IL1RN protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266802026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq29118-sds-page.jpgPorcine recombinant GM-CSF protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266812026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp27169-1-sds-page.jpgHuman recombinant PON1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266822026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp70193-sds-page.jpgMouse recombinant LRIG1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266832026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp19801-1-sds-page.jpgHuman recombinant ABP1/AOC1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266842026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12643-6-sds-page.jpgHuman recombinant BMP-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266852026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq12794-1-sds-page.jpgHuman recombinant Hyaluronidase 1/HYAL1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266862026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp39905-2-sds-page.jpgHuman recombinant GDNF protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266872026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq06124-1-sds-page.jpgHuman recombinant SHP-2/PTPN11 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266882026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12821-sds-page.jpgHuman recombinant ACE Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266892026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07214-sds-page.jpgMouse recombinant SPARC protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266902026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6vns1-sds-page.jpgMouse recombinant TrkC Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266912026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq02763-2-sds-page.jpgHuman recombinant TIE2/TEK protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266922026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp0dml2-sds-page.jpgHuman recombinant Placental Lactogen/CSH1 Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266932026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq60846-sds-page.jpgMouse recombinant?CD30/TNFRSF8 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266942026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto08722-sds-page.jpgRat recombinant UNC5H2/UNC5B protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266952026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10451-4-sds-page.jpgHuman recombinant Osteopontin/OPN protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266962026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp48551-sds-page.jpgHuman recombinant IFN-alpha/beta R2/IFNAR2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266972026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8ce08-sds-page.jpgMouse recombinant?Prostatic Acid Phosphatase/ACPP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266982026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nr61-1-sds-page.jpgHuman recombinant DLL4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1266992026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9eqf2-sds-page.jpgMouse recombinant Kell protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267002026-03-10T04:37:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq2vce2-sds-page.jpgCanine recombinant IL-1 beta/IL1B protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267012026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9umf0-sds-page.jpgHuman recombinant ICAM-5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267022026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp42703-sds-page.jpgMouse recombinant LIFR alpha/LIFR Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267032026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07321-sds-page.jpgMouse recombinant Erythropoietin/EPO Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267042026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp59594-sds-page.jpgRecombinant SARS-CoV Spike RBD protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267052026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9byf1-sds-page.jpgHuman recombinant ACE-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267062026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto54901-1-sds-page.jpgMouse recombinant CD200 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267072026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8nhl6-sds-page.jpgHuman recombinant LILRB1/CD85j/ILT2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267082026-04-03T05:00:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp59594-1-sds-page.jpgRecombinant SARS-CoV Spike RBD protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267092026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp59594-2-sds-page.jpgRecombinant SARS-CoV Spike protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267102026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp40225-5-sds-page.jpgHuman recombinant Thrombopoietin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267112026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp47741-sds-page.jpgMouse recombinant OX40/TNFRSF4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267122026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95750-3-sds-page.jpgHuman recombinant FGF-19 Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267132026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp97299-sds-page.jpgMouse recombinant sFRP-2/SFRP2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267142026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6l7i9-sds-page.jpgCanine recombinant IL-21 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267152026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq99p68-sds-page.jpgMouse recombinant SOST/Sclerostin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267162026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto46612-sds-page.jpgCanine recombinant IL-1 alpha/IL1A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267172026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9hd89-7-sds-page.jpgHuman recombinant Resistin/RETN protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267182026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01833-1-sds-page.jpgHuman recombinant pIgR protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267192026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protk0brg7-sds-page.jpgRecombinant MERS-CoV Spike protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267202026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protk0brg7-1-sds-page.jpgRecombinant MERS-CoV Spike S1 Subunit protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267212026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protk0brg7-2-sds-page.jpgRecombinant MERS-CoV Spike S2 Subunit protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267222026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protk0brg7-3-sds-page.jpgRecombinant MERS-CoV Spike RBD protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267232026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05112-8-sds-page.jpgHuman recombinant IL-4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267242026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq3u0p5-sds-page.jpgMouse recombinant CD39L2/ENTPD6 Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267252026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq95j76-sds-page.jpgCanine recombinant IL-5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267262026-03-10T04:37:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14207-sds-page.jpgHuman recombinant FOLR2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267272026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq12884-1-sds-page.jpgHuman recombinant FAP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267282026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp18428-1-sds-page.jpgHuman recombinant LBP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267292026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq02297-2-sds-page.jpgHuman recombinant NRG1/HRG1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267302026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13591-sds-page.jpgHuman recombinant NCAM-1/CD56 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267312026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8vim0-sds-page.jpgMouse recombinant TIM-3/HAVCR2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267322026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp02741-4-sds-page.jpgHuman recombinant C-Reactive/CRP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267332026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16581-3-sds-page.jpgHuman recombinant E-selectin/CD62E protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267342026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9qup4-sds-page.jpgMouse recombinant CHST5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267352026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07204-1-sds-page.jpgHuman recombinant Thrombomodulin/BDCA-3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267362026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9h2x3-1-sds-page.jpgHuman recombinant CD299/CLEC4M protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267372026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq14242-2-sds-page.jpgHuman recombinant PSGL-1/CD162 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267382026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp29676-sds-page.jpgRat recombinant Erythropoietin/EPO protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267392026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq7lgc8-sds-page.jpgHuman recombinant Carbohydrate sulfotransferase 3/CHST3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267402026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14844-2-sds-page.jpgRat recombinant CCL2/MCP-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267412026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq32mv9-sds-page.jpgMouse recombinant BTLA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267422026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp31997-sds-page.jpgHuman recombinant CD66b/CEACAM8 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267432026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp30203-sds-page.jpgHuman recombinant CD6 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267442026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp25942-2-sds-page.jpgHuman recombinant CD40/TNFRSF5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267452026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9y5y7-4-sds-page.jpgHuman recombinant LYVE-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267462026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9bzm4-1-sds-page.jpgHuman recombinant ULBP-3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267472026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nnx6-sds-page.jpgHuman recombinant DC-SIGN/CD209 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267482026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9bqb4-1-sds-page.jpgHuman recombinant SOST/Sclerostin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267492026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp59594-3-sds-page.jpgRecombinant SARS-CoV S1 Subunit protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267502026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41217-4-sds-page.jpgHuman recombinant CD200 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267512026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8r0i0-1-sds-page.jpgMouse recombinant ACE-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267522026-03-10T04:37:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq08722-4-sds-page.jpgHuman recombinant CD47 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267532026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp35070-4-sds-page.jpgHuman recombinant Betacellulin/BTC Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267542026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq93038-2-sds-page_1.jpgHuman recombinant DR3/TNFRSF25 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain https://www.bosterbio.com/catalog/product/view/id/1267552026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9h293-2-sds-page.jpgHuman recombinant IL-17E/IL-25 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267562026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp29965-4-sds-page.jpgHuman recombinant CD40 Ligand/CD40LG protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267572026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq13253-5-sds-page.jpgHuman recombinant Noggin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267582026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp43488-sds-page.jpgMouse recombinant OX40 Ligand/TNFSF4 Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267592026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq5vy80-sds-page.jpgHuman recombinant ULBP-6/RAET1L Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267602026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9uhd0-2-sds-page.jpgHuman recombinant IL-19 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267612026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49763-9-sds-page.jpgHuman recombinant PIGF-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267622026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9ubx1-2-sds-page.jpgHuman recombinant Cathepsin F protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267632026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq15116-2-sds-page.jpgHuman recombinant PD-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267642026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp04401-2-sds-page.jpgMouse recombinant IL-5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267652026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp04401-3-sds-page.jpgMouse recombinant IL-5 Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267662026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9p1w8-4-sds-page.jpgHuman recombinant SIRP gamma/CD172g protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267672026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6vab8-sds-page.jpgPorcine recombinant IFN-alpha 1/IFNA1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267682026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp32004-2-sds-page.jpgHuman recombinant L1CAM protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267692026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp63302-2-sds-page.jpgHuman recombinant Selenoprotein W/SELENOW protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267702026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota0a024e3p0-sds-page.jpgRecombinant Influenza A H7N9 Hemagglutinin/HA1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267712026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9z1t2-sds-page.jpgMouse recombinant Thrombospondin 4/THBS4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267722026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto75594-1-sds-page.jpgHuman recombinant PGLYRP1/PGRP-S protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267732026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49747-1-sds-page.jpgHuman recombinant Thrombospondin 5/COMP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267742026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp54762-sds-page.jpgHuman recombinant EphB1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267752026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nrm6-2-sds-page.jpgHuman recombinant IL-17RB protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267762026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12032-2-sds-page.jpgMouse recombinant TIMP-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267772026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp52564-4-sds-page.jpgHuman recombinant MKK6 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267782026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8n423-1-sds-page.jpgHuman recombinant LILRB2/CD85d/ILT4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267792026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41324-1-sds-page.jpgCanine recombinant IL-8/CXCL8 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267802026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq15303-sds-page.jpgHuman recombinant ErbB4/Her4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267812026-03-10T04:37:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp43489-2-sds-page.jpgHuman recombinant OX40/TNFRSF4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267822026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09793-1-sds-page.jpgMouse recombinant CTLA4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267832026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp67870-2-sds-page.jpgHuman recombinant Casein kinase 2 beta/CSNK2B protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267842026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq5egz1-1-sds-page.jpgRat recombinant ACE-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267852026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9es17-2-sds-page.jpgMouse recombinant IL-21 Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267862026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp00797-5-sds-page.jpgHuman recombinant Renin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267872026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07998-sds-page.jpgHuman recombinant Ribonuclease A/RNASE 1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267882026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10923-sds-page.jpgMouse recombinant Osteopontin/OPN protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267892026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq04609-sds-page.jpgHuman recombinant Folate hydrolase 1/FOLH1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267902026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp0a7y8-sds-page.jpgE.coli recombinant rnpA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267912026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq61490-sds-page.jpgMouse recombinant ALCAM/CD166 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267922026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9jhx3-sds-page.jpgMouse recombinant IL-21R protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267932026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq13822-sds-page.jpgHuman recombinant ENPP-2/Autotaxin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267942026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp22303-1-sds-page.jpgHuman recombinant Acetylcholinesterase/ACHE protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267952026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq99985-sds-page.jpgHuman recombinant Semaphorin 3C(R551A/R552A/R611A/R612A) protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267962026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26842-4-sds-page.jpgHuman recombinant TNFRSF7/CD27 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267972026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9y243-1-sds-page.jpgHuman recombinant Akt3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267982026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp35590-1-sds-page.jpgHuman recombinant TIE1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1267992026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nzs2-sds-page.jpgHuman recombinant NKp80/KLRF1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268002026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp21926-2-sds-page.jpgHuman recombinant CD9 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268012026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10153-sds-page.jpgHuman recombinant RNASE2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268022026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto14944-4-sds-page.jpgHuman recombinant Epiregulin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268032026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13500-4-sds-page.jpgHuman recombinant CCL2/MCP-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268042026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protc6l8d7-sds-page.jpgCanine recombinant IL-17A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268052026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp78324-2-sds-page.jpgHuman recombinant SIRP alpha/CD172a protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268062026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq08722-5-sds-page.jpgHuman recombinant CD47 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268072026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto54908-sds-page.jpgMouse recombinant DKK1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268082026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp52803-2-sds-page.jpgHuman recombinant Ephrin-A5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268092026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95256-1-sds-page.jpgHuman recombinant IL-18R beta/IL18RAP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268102026-03-10T04:37:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14415-4-sds-page.jpgHuman recombinant ATP1B2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268112026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nsp4-2-sds-page.jpgHuman recombinant CENPM protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268122026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq06599-1-sds-page.jpgBovine recombinant TNF-alpha protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268132026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16435-2-sds-page.jpgHuman recombinant Cytochrome p450 reductase/POR protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268142026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05120-4-sds-page.jpgHuman recombinant Serpin B2/PAI-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268152026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8td30-4-sds-page.jpgHuman recombinant ALT2/GPT2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268162026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41743-1-sds-page.jpgHuman recombinant PKC iota protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268172026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto43827-1-sds-page.jpgHuman recombinant Angiopoietin-like 7/ANGPTL7 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268192026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95150-4-sds-page.jpgHuman recombinant TL1A/TNFSF15 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268202026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp35739-sds-page.jpgRat recombinant TrkA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268212026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07339-1-sds-page.jpgHuman recombinant Cathepsin D protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268232026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp42785-sds-page.jpgHuman recombinant PRCP protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268242026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp02763-3-sds-page.jpgHuman recombinant Alpha 1-Acid Glycoprotein 1/ORM1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268252026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto00592-sds-page.jpgHuman recombinant Podocalyxin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268262026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26952-sds-page.jpgMouse recombinant IL-3R alpha/IL3RA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268272026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq08481-sds-page.jpgMouse recombinant CD31/PECAM1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268282026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp97821-sds-page.jpgMouse recombinant Cathepsin C/DPPI protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268292026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01857-1-sds-page.jpgHuman recombinant IgG1 Fc protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268302026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08571-5-sds-page.jpgHuman recombinant CD14 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268312026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp00352-2-sds-page.jpgHuman recombinant Aldehyde Dehydrogenase 1-A1/ ALDH1A1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268322026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp55075-3-sds-page.jpgHuman recombinant FGF-8b protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268332026-03-10T04:37:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08637-4-sds-page.jpgHuman recombinant CD16a/FCGR3A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268342026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq96rq9-sds_3.jpgHuman recombinant IL-4I1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain https://www.bosterbio.com/catalog/product/view/id/1268352026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq68d85-1-sds-page.jpgHuman recombinant B7-H6 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268362026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp17948-7-sds-page.jpgHuman recombinant VEGFR1/Flt-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268372026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08637-5-sds-page.jpgHuman recombinant CD16a/FCGR3A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268382026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08833-2-sds-page.jpgHuman recombinant IGFBP-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268392026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nzc2-2-sds-page.jpgHuman recombinant TREM2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268402026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protc7g0w1-3-sds-page.jpgCanine recombinant IL31 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268412026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp50282-sds-page.jpgRat recombinant MMP-9 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268422026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16435-3-sds-page.jpgHuman recombinant POR protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268432026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01730-5-sds-page.jpgHuman recombinant CD4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268442026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp27487-3-sds-page.jpgHuman recombinant CD26/DPP4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268452026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9jl18-sds-page.jpgMouse recombinant BACE-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268462026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protk0brg7-4-sds-page.jpgRecombinant MERS-CoV Spike RBD protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268472026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protk0brg7-5-sds-page.jpgRecombinant MERS-CoV Spike protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268482026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05362-5-sds-page.jpgHuman recombinant ICAM-1/CD54 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268492026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13224-sds-page.jpgHuman recombinant GP1BB protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268502026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9ns85-1-sds-page.jpgHuman recombinant Carbonic Anhydrase X/CA10 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268512026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12318-1-sds-page.jpgHuman recombinant Fc gamma RIIA/CD32a (R167H) protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268522026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09038-8-sds-page.jpgHuman recombinant FGF basic/FGF-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268532026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp06151-2-sds-page.jpgMouse recombinant Lactate Dehydrogenase A/LDHA protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268542026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13597-1-sds-page.jpgMouse recombinant ICAM-1/CD54 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268552026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq62386-3-sds-page.jpgMouse recombinant IL-17A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268562026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10915-2-sds-page.jpgHuman recombinant HAPLN1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268572026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05067-2-sds-page.jpgHuman recombinant APP/Protease Nexin II protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268582026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq99645-sds-page.jpgHuman recombinant DSPG3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268592026-03-10T04:37:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12319-3-sds-page.jpgHuman recombinant Fc epsilon RI alpha protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268602026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05186-sds-page.jpgHuman recombinant Alkaline Phosphatase/ALPL protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268612026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8bif0-sds-page.jpgMouse recombinant CD99-L2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268622026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41245-1-sds-page.jpgMouse recombinant MMP-9 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268632026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14735-1-sds-page.jpgHuman recombinant Insulysin/IDE protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268642026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp21815-2-sds-page.jpgHuman recombinant IBSP/Sialoprotein II protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268652026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp35030-4-sds-page.jpgHuman recombinant Trypsin 3/PRSS3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268662026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq96rj3-2-sds-page.jpgHuman recombinant BAFF R/TNFRSF13C protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268672026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nzu0-2-sds-page.jpgHuman recombinant FLRT3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268682026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05000-2-sds-page.jpgHuman recombinant IFN-omega protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268692026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp36897-1-sds-page.jpgHuman recombinant TGF-beta RI/ALK-5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268702026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq16534-2-sds-page.jpgHuman recombinant HLF protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268712026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp23510-1-sds-page.jpgHuman recombinant OX40 Ligand/TNFSF4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268722026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp02511-2-sds-page.jpgHuman recombinant Crystallin alpha B/CRYAB protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268732026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp55899-1-sds-page.jpgHuman recombinant FCRN/FCGRT&B2M protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268742026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9y275-5-sds-page.jpgHuman recombinant BAFF/TNFSF13B protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268752026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49763-10-sds-page.jpgHuman recombinant PlGF-1/PGF protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268762026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp47741-1-sds-page.jpgMouse recombinant OX40/TNFRSF4 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268772026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq96bf3-1-sds-page.jpgHuman recombinant TMIGD2/CD28H protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268782026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49763-11-sds-page.jpgHuman recombinant PIGF-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268792026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp47877-sds-page.jpgMouse recombinant IGFBP-2 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268802026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq92854-2-sds-page.jpgHuman recombinant semaphorin-4D protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268812026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp37173-3-sds-page.jpgHuman recombinant TGF-beta RII protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268822026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp52803-3-sds-page.jpgHuman recombinant Ephrin-A5 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268832026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8brb1-sds-page.jpgMouse recombinant EphA3 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268842026-03-10T04:37:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp31994-2-sds-page.jpgHuman recombinant Fc gamma RIIB/CD32b protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268852026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp61366-1-sds-page.jpgHuman recombinant Osteocrin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268862026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9ulw2-sds-page.jpgHuman recombinant Frizzled-10 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268872026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq16620-2-sds-page.jpgHuman recombinant TrkB protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268882026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01133-4-sds-page.jpgHuman recombinant Animal Free EGF protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268892026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp56159-1-sds-page.jpgHuman recombinant GFR alpha-1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268902026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto35305-sds-page.jpgMouse recombinant RANK/TNFRSF11A protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268912026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp55786-sds-page.jpgHuman recombinant NPEPPS protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268922026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01009-1.jpgHuman recombinant Serpin A1/alpha 1-Antitrypsin protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268932026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto00559-1.jpgHuman recombinant EBAG9 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/catalog/product/view/id/1268942026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01562-1.jpgHuman recombinant IFN-alpha 1/IFNA1 protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain. https://www.bosterbio.com/products/consumables/transfer-caps-for-erlenmeyer-flasks-without-flasks-cs0015-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0015-transfer_caps-for-erlenmeyer-flasks-1.jpgTransfer Caps for Erlenmeyer Flasks, without flasks https://www.bosterbio.com/products/consumables/closed-systems-for-media-bottles-with-bottles-cs0016-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0016-closed-systems-for-media_bottles-with-bottles-1.jpgClosed Systems for Media Bottles, with bottles https://www.bosterbio.com/products/consumables/transfer-caps-for-media-bottles-withou-bottles-cs0017-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0017-closed-systems-for-media_bottles-without-_bottles-1.jpgTransfer Caps for Media Bottles, without bottles https://www.bosterbio.com/products/consumables/closed-systems-for-centrifuge-tubes-with-tubes-cs0018-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0018-closed-systems-for-centrifuge-tubes-with_tubes-1.pngClosed Systems for centrifuge tubes, with tubeshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0018-closed-systems-for-centrifuge-tubes-with_tubes-2.pngClosed Systems for centrifuge tubes, with tubeshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0018-closed-systems-for-centrifuge-tubes-with_tubes-3.pngClosed Systems for centrifuge tubes, with tubeshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0018-closed-systems-for-centrifuge-tubes-with_tubes-4.pngClosed Systems for centrifuge tubes, with tubes https://www.bosterbio.com/products/consumables/serological-pipettes-cs0019-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0019-serological-pipettes-1.jpgSerological Pipetteshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0019-serological-pipettes-2.jpgSerological Pipetteshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0019-serological-pipettes-3.jpgSerological 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Scrapershttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0021-cell_scrapers-3.jpgCell Scrapers https://www.bosterbio.com/products/consumables/glass-bottom-cell-cutlure-dishes-plates-cs0022-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0022glass-bottom-cell-culture-dish-plate-1.jpgGlass Bottom Cell Cutlure Dishes/ Plateshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0022glass-bottom-cell-culture-dish-plate-2.jpgGlass Bottom Cell Cutlure Dishes/ Plateshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0022glass-bottom-cell-culture-dish-plate-3.jpgGlass Bottom Cell Cutlure Dishes/ Plateshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0022glass-bottom-cell-culture-dish-plate-4.jpgGlass Bottom Cell Cutlure 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https://www.bosterbio.com/products/consumables/15ml-50ml-centrifuge-tubes-standard-cs0024-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0024-centrifuge-tubes-1.jpg15ml & 50ml Centrifuge Tubes, standardhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0024-centrifuge-tubes-2.jpg15ml & 50ml Centrifuge Tubes, standardhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0024-centrifuge-tubes-3.jpg15ml & 50ml Centrifuge Tubes, standardhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0024-centrifuge-tubes-4.jpg15ml & 50ml Centrifuge Tubes, standard https://www.bosterbio.com/products/consumables/peripheral-blood-lymphocyte-separation-tube-cs0025-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0025-pbmc-separation-tube-1.pngPeripheral Blood Lymphocyte Separation Tubehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0025-pbmc-separation-tube-2.pngPeripheral Blood Lymphocyte Separation Tubehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0025-pbmc-separation-tube-3.pngPeripheral Blood Lymphocyte Separation Tubehttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0025-pbmc-separation-tube-4.pngPeripheral Blood Lymphocyte Separation Tube https://www.bosterbio.com/products/consumables/250ml-500ml-centrifuge-tubes-cs0026-boster.html2026-03-10T04:37:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0026-250ml_500ml-centrifuge-tubes-1.png250mL&500mL Centrifuge Tubeshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0026-250ml_500ml-centrifuge-tubes-2.png250mL&500mL Centrifuge Tubes https://www.bosterbio.com/products/consumables/microcentrifuge-tubes-cs0027-boster.html2026-03-10T04:37:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0027-microcentrifuge-tubes-1.jpgMicrocentrifuge Tubes https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0027-microcentrifuge-tubes-2.jpgMicrocentrifuge Tubes https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0027-microcentrifuge-tubes-3.jpgMicrocentrifuge Tubes https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0027-microcentrifuge-tubes-4.jpgMicrocentrifuge Tubes https://www.bosterbio.com/products/consumables/micro-tube-boxes-cs0028-boster.html2026-03-10T04:37:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0028-micro-tube-boxes-1.jpgMicro Tube Boxeshttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0028-micro-tube-boxes-2.jpgMicro Tube Boxes https://www.bosterbio.com/products/consumables/pasteur-pipets-cs0029-boster.html2026-03-10T04:37:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/c/s/cs0029-pasteur-pipets-1.jpgPasteur 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https://www.bosterbio.com/catalog/product/view/id/1269702026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01085-1-atp7a-primary-antibodies-wb-testing-1.jpgAnti-ATP7A Antibody Picoband® Western blot analysis of ATP7A using anti-ATP7A antibody (A01085-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATP7A antigen affinity purified polyclonal antibody (Catalog # A01085-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATP7A at approximately 163 kDa. The expected band size for ATP7A is at 163 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01085-1-atp7a-primary-antibodies-fcm-testing-2.jpgAnti-ATP7A Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ATP7A antibody (A01085-1). Overlay histogram showing HepG2 cells stained with A01085-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ATP7A Antibody (A01085-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269712026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02341-alox5ap-primary-antibodies-wb-testing-1.jpgAnti-ALOX5AP Antibody Picoband® Western blot analysis of ALOX5AP using anti-ALOX5AP antibody (A02341). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Raji whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ALOX5AP antigen affinity purified polyclonal antibody (Catalog # A02341) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ALOX5AP at approximately 18 kDa. The expected band size for ALOX5AP is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02341-alox5ap-primary-antibodies-ihc-testing-1.jpgAnti-ALOX5AP Antibody Picoband®IHC analysis of ALOX5AP using anti-ALOX5AP antibody (A02341). ALOX5AP was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ALOX5AP Antibody (A02341) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02341-alox5ap-primary-antibodies-if-testing-2.jpgAnti-ALOX5AP Antibody Picoband® IF analysis of ALOX5AP using anti-ALOX5AP antibody (A02341). ALOX5AP was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ALOX5AP Antibody (A02341) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02341-alox5ap-primary-antibodies-fcm-testing-3.jpgAnti-ALOX5AP Antibody Picoband® Flow Cytometry analysis of JK cells using anti-ALOX5AP antibody (A02341). Overlay histogram showing JK cells stained with A02341 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ALOX5AP Antibody (A02341, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269722026-03-17T05:16:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07527-1-apobec3c-primary-antibodies-wb-testing-1.jpgAnti-APOBEC3C Antibody Picoband® Western blot analysis of APOBEC3C using anti-APOBEC3C antibody (A07527-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat spleen tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse spleen tissue lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-APOBEC3C antigen affinity purified polyclonal antibody (Catalog # A07527-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for APOBEC3C at approximately 23 kDa. The expected band size for APOBEC3C is at 23 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07527-1-apobec3c-primary-antibodies-ihc-testing-2.jpgAnti-APOBEC3C Antibody Picoband® IHC analysis of APOBEC3C using anti-APOBEC3C antibody (A07527-1). APOBEC3C was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APOBEC3C Antibody (A07527-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07527-1-apobec3c-primary-antibodies-ihc-testing-3.jpgAnti-APOBEC3C Antibody Picoband® IHC analysis of APOBEC3C using anti-APOBEC3C antibody (A07527-1). APOBEC3C was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APOBEC3C Antibody (A07527-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07527-1-apobec3c-primary-antibodies-ihc-testing-4.jpgAnti-APOBEC3C Antibody Picoband® IHC analysis of APOBEC3C using anti-APOBEC3C antibody (A07527-1). APOBEC3C was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-APOBEC3C Antibody (A07527-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07527-1-apobec3c-primary-antibodies-if-testing-5.jpgAnti-APOBEC3C Antibody Picoband® IF analysis of APOBEC3C using anti-APOBEC3C antibody (A07527-1) and anti-Beta Tubulin antibody (M01857-3). APOBEC3C was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-APOBEC3C Antibody (A07527-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07527-1-apobec3c-primary-antibodies-fcm-testing-6.jpgAnti-APOBEC3C Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-APOBEC3C antibody (A07527-1). Overlay histogram showing K562 cells stained with A07527-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-APOBEC3C Antibody (A07527-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269732026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08342-1-arpin-primary-antibodies-wb-testing-1.jpgAnti-ARPIN Antibody Picoband® Western blot analysis of ARPIN using anti-ARPIN antibody (A08342-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARPIN antigen affinity purified polyclonal antibody (Catalog # A08342-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARPIN at approximately 35 kDa. The expected band size for ARPIN is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08342-1-arpin-primary-antibodies-fcm-testing-2.jpgAnti-ARPIN Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-ARPIN antibody (A08342-1). Overlay histogram showing U251 cells stained with A08342-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ARPIN Antibody (A08342-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269742026-04-06T05:04:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03023-2-ascl1-primary-antibodies-wb-testing-1.jpgAnti-ASCL1 Antibody Picoband® Western blot analysis of ASCL1 using anti-ASCL1 antibody (A03023-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human NCL-H460 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ASCL1 antigen affinity purified polyclonal antibody (Catalog # A03023-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ASCL1 at approximately 30 kDa. The expected band size for ASCL1 is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03023-2-ascl1-primary-antibodies-ihc-testing-2.jpgAnti-ASCL1 Antibody Picoband® IHC analysis of ASCL1 using anti-ASCL1 antibody (A03023-2). ASCL1 was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-ASCL1 Antibody (A03023-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03023-2-ascl1-primary-antibodies-fcm-testing-3.jpgAnti-ASCL1 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-ASCL1 antibody (A03023-2). Overlay histogram showing K562 cells stained with A03023-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ASCL1 Antibody (A03023-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269752026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02792-1-atf5-primary-antibodies-wb-testing-1.jpgAnti-ATF5 Antibody Picoband® Western blot analysis of ATF5 using anti-ATF5 antibody (A02792-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: rat RH35 whole cell lysates, Lane 7: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ATF5 antigen affinity purified polyclonal antibody (Catalog # A02792-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ATF5 at approximately 37 kDa. The expected band size for ATF5 is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02792-1-atf5-primary-antibodies-fcm-testing-2.jpgAnti-ATF5 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-ATF5 antibody (A02792-1). Overlay histogram showing 293T cells stained with A02792-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ATF5 Antibody (A02792-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269762026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02592-3-tcf12-primary-antibodies-wb-testing-1.jpgAnti-HEB/TCF12 Antibody Picoband® Western blot analysis of HEB/TCF12 using anti-HEB/TCF12 antibody (A02592-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HEB/TCF12 antigen affinity purified polyclonal antibody (Catalog # A02592-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HEB/TCF12 at approximately 85 kDa. The expected band size for HEB/TCF12 is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02592-3-tcf12-primary-antibodies-fcm-testing-2.jpgAnti-HEB/TCF12 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-HEB/TCF12 antibody (A02592-3). Overlay histogram showing 293T cells stained with A02592-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-HEB/TCF12 Antibody (A02592-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269772026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10356-2-lmod3-primary-antibodies-wb-testing-1.jpgAnti-LMOD3 Antibody Picoband® Western blot analysis of LMOD3 using anti-LMOD3 antibody (A10356-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skeletal muscle tissue lysates, Lane 2: mouse heart tissue lysates, Lane 3: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMOD3 antigen affinity purified polyclonal antibody (Catalog # A10356-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for LMOD3 at approximately 70 kDa. The expected band size for LMOD3 is at 65 kDa. https://www.bosterbio.com/catalog/product/view/id/1269782026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01778-3-txnrd1-primary-antibodies-wb-testing-1.jpgAnti-TXNRD1 Antibody Picoband® Western blot analysis of TXNRD1 using anti-TXNRD1 antibody (A01778-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human A549 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TXNRD1 antigen affinity purified polyclonal antibody (Catalog # A01778-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TXNRD1 at approximately 65 kDa. The expected band size for TXNRD1 is at 71 kDa. https://www.bosterbio.com/catalog/product/view/id/1269792026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05317-1-arhgef6-primary-antibodies-wb-testing-1.jpgAnti-ARHGEF6 Antibody Picoband® Western blot analysis of ARHGEF6 using anti-ARHGEF6 antibody (A05317-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ARHGEF6 antigen affinity purified polyclonal antibody (Catalog # A05317-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ARHGEF6 at approximately 87 kDa. The expected band size for ARHGEF6 is at 87 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05317-1-arhgef6-primary-antibodies-fcm-testing-2.jpgAnti-ARHGEF6 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-ARHGEF6 antibody (A05317-1). Overlay histogram showing PC-3 cells stained with A05317-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-ARHGEF6 Antibody (A05317-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269802026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02754-1-gatm-primary-antibodies-wb-testing-1.jpgAnti-GATM Antibody Picoband® Western blot analysis of GATM using anti-GATM antibody (A02754-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human AGS whole cell lysates, Lane 2: human HUH-7 whole cell lysates, Lane 3: rat kidney tissue lysates, Lane 4: rat HBZY-1 whole cell lysates, Lane 5: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GATM antigen affinity purified polyclonal antibody (Catalog # A02754-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GATM at approximately 48 kDa. The expected band size for GATM is at 48 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02754-1-gatm-primary-antibodies-ihc-testing-2.jpgAnti-GATM Antibody Picoband® IHC analysis of GATM using anti-GATM antibody (A02754-1). GATM was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GATM Antibody (A02754-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02754-1-gatm-primary-antibodies-ihc-testing-3.jpgAnti-GATM Antibody Picoband® IHC analysis of GATM using anti-GATM antibody (A02754-1). GATM was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GATM Antibody (A02754-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02754-1-gatm-primary-antibodies-ihc-testing-4.jpgAnti-GATM Antibody Picoband® IHC analysis of GATM using anti-GATM antibody (A02754-1). GATM was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GATM Antibody (A02754-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02754-1-gatm-primary-antibodies-if-testing-1.jpgAnti-GATM Antibody Picoband®IF analysis of GATM using anti-GATM antibody (A02754-1). GATM was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-GATM Antibody (A02754-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02754-1-gatm-primary-antibodies-fcm-testing-5.jpgAnti-GATM Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-GATM antibody (A02754-1). Overlay histogram showing THP-1 cells stained with A02754-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GATM Antibody (A02754-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269812026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08835-1-adh6-primary-antibodies-wb-testing-1.jpgAnti-ADH6 Antibody Picoband® Western blot analysis of ADH6 using anti-ADH6 antibody (A08835-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ADH6 antigen affinity purified polyclonal antibody (Catalog # A08835-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for ADH6 at approximately 39 kDa. The expected band size for ADH6 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08835-1-adh6-primary-antibodies-fcm-testing-2.jpgAnti-ADH6 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-ADH6 antibody (A08835-1). Overlay histogram showing HepG2 cells stained with A08835-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ADH6 Antibody (A08835-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269822026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04209-1-ampd1-primary-antibodies-wb-testing-1.jpgAnti-AMPD1 Antibody Picoband® Western blot analysis of AMPD1 using anti-AMPD1 antibody (A04209-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat heart tissue lysates, Lane 4: rat skeletal muscle tissue lysates, Lane 5: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-AMPD1 antigen affinity purified polyclonal antibody (Catalog # A04209-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for AMPD1 at approximately 86 kDa. The expected band size for AMPD1 is at 86 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04209-1-ampd1-primary-antibodies-ihc-testing-2.jpgAnti-AMPD1 Antibody Picoband® IHC analysis of AMPD1 using anti-AMPD1 antibody (A04209-1). AMPD1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AMPD1 Antibody (A04209-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04209-1-ampd1-primary-antibodies-ihc-testing-3.jpgAnti-AMPD1 Antibody Picoband® IHC analysis of AMPD1 using anti-AMPD1 antibody (A04209-1). AMPD1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-AMPD1 Antibody (A04209-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04209-1-ampd1-primary-antibodies-fcm-testing-4.jpgAnti-AMPD1 Antibody Picoband® Flow Cytometry analysis of U251 cells using anti-AMPD1 antibody (A04209-1). Overlay histogram showing U251 cells stained with A04209-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-AMPD1 Antibody (A04209-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269832026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-3-arhgef2-primary-antibodies-wb-testing-1.jpgAnti-GEF-H1/ARHGEF2 Antibody Picoband® Western blot analysis of GEF-H1/ARHGEF2 using anti-GEF-H1/ARHGEF2 antibody (A02572-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse Raw264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GEF-H1/ARHGEF2 antigen affinity purified polyclonal antibody (Catalog # A02572-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GEF-H1/ARHGEF2 at approximately 112 kDa. The expected band size for GEF-H1/ARHGEF2 is at 112 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-3-arhgef2-primary-antibodies-ihc-testing-2.jpgAnti-GEF-H1/ARHGEF2 Antibody Picoband® IHC analysis of GEF-H1/ARHGEF2 using anti-GEF-H1/ARHGEF2 antibody (A02572-3). GEF-H1/ARHGEF2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GEF-H1/ARHGEF2 Antibody (A02572-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-3-arhgef2-primary-antibodies-ihc-testing-3.jpgAnti-GEF-H1/ARHGEF2 Antibody Picoband® IHC analysis of GEF-H1/ARHGEF2 using anti-GEF-H1/ARHGEF2 antibody (A02572-3). GEF-H1/ARHGEF2 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GEF-H1/ARHGEF2 Antibody (A02572-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-3-arhgef2-primary-antibodies-ihc-testing-4.jpgAnti-GEF-H1/ARHGEF2 Antibody Picoband® IHC analysis of GEF-H1/ARHGEF2 using anti-GEF-H1/ARHGEF2 antibody (A02572-3). GEF-H1/ARHGEF2 was detected in a paraffin-embedded section of human ovary cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GEF-H1/ARHGEF2 Antibody (A02572-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02572-3-arhgef2-primary-antibodies-fcm-testing-5.jpgAnti-GEF-H1/ARHGEF2 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-GEF-H1/ARHGEF2 antibody (A02572-3). Overlay histogram showing PC-3 cells stained with A02572-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GEF-H1/ARHGEF2 Antibody (A02572-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269842026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02090-2-bgn-primary-antibodies-wb-testing-1.jpgAnti-Biglycan/BGN Antibody Picoband® Western blot analysis of Biglycan/BGN using anti-Biglycan/BGN antibody (A02090-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human COLO320 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human HUVEC whole cell lysates, Lane 5: rat skeletal muscle tissue lysates, Lane 6: rat L6 whole cell lysates, Lane 7: mouse skeletal muscle tissue lysates, Lane 8: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Biglycan/BGN antigen affinity purified polyclonal antibody (Catalog # A02090-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Biglycan/BGN at approximately 48 kDa. The expected band size for Biglycan/BGN is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02090-2-bgn-primary-antibodies-ihc-testing-2.jpgAnti-Biglycan/BGN Antibody Picoband® IHC analysis of Biglycan/BGN using anti-Biglycan/BGN antibody (A02090-2). Biglycan/BGN was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Biglycan/BGN Antibody (A02090-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02090-2-bgn-primary-antibodies-ihc-testing-3.jpgAnti-Biglycan/BGN Antibody Picoband® IHC analysis of Biglycan/BGN using anti-Biglycan/BGN antibody (A02090-2). Biglycan/BGN was detected in a paraffin-embedded section of rat knee tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Biglycan/BGN Antibody (A02090-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02090-2-bgn-primary-antibodies-fcm-testing-4.jpgAnti-Biglycan/BGN Antibody Picoband® Flow Cytometry analysis of Caco-2 cells using anti-Biglycan/BGN antibody (A02090-2). Overlay histogram showing Caco-2 cells stained with A02090-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Biglycan/BGN Antibody (A02090-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1269852026-03-10T04:38:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/o/boster-box_17.pngWash Buffer (25x)Boster Kit Box https://www.bosterbio.com/products/all-secondary-antibodies/unconjugated-affinipure-mouse-anti-rabbit-igg-bm2020-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/biotin-conjugated-affinipure-mouse-anti-digoxin-igg-bm0040-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/hrp-conjugated-affinipure-mouse-anti-rabbit-igg-bm2006-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/hrp-conjugated-affinipure-mouse-anti-human-igg-bm2002-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/hrp-conjugated-affinipure-goat-anti-mouse-rabbit-igg-ba1056-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/hrp-conjugated-affinipure-rabbit-anti-guinea-pig-igg-ba1059-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/dyl488-conjugated-affinipure-rabbit-anti-rat-igg-ba1129-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/cy3-conjugated-affinipure-rabbit-anti-rat-igg-ba1036-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/dyl488-conjugated-affinipure-rabbit-anti-goat-igg-ba1124-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/dyl488-conjugated-avidin-ba1143-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/dyl550-conjugated-goat-anti-mouse-igg-ba1133-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/dyl550-conjugated-goat-anti-rabbit-igg-ba1135-boster.html2026-03-10T04:38:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/b/a/ba1135-1.jpgAffiniPure Goat Anti-rabbit IgG (H+L) secondary antibody, Fluoro550 ConjugatedIF analysis of PKC gamma using anti-PKC gamma antibody (A01890). PKC gamma was detected in a paraffin-embedded section of rat celebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-PKC gamma Antibody (A01890) overnight at 4°C. Fluoro550 conjugated goat anti-rabbit IgG (BA1035) was used as secondary antibody and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/products/all-secondary-antibodies/dyl550-conjugated-avidin-ba1134-boster.html2026-03-10T04:38:00+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/fitc-conjugated-mouse-anti-rabbit-igg-bm2012-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/tritc-conjugated-mouse-anti-human-igg-ba1094-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/all-secondary-antibodies/cy3-conjugated-protein-a-ba1033-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1270042026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2287.jpgHuman/Canine/Porcine Insulin ELISA Kit PicoKine®Human/Canine/Porcine Insulin ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1270052026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2288.pngHuman C-Peptide ELISA Kit PicoKine®Human C-Peptide ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1270062026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek1552.jpgHuman MEP1A ELISA Kit PicoKine®Human MEP1A ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1270072026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek2289.jpgHuman/Mouse COX-2 ELISA Kit PicoKine®Human/Mouse COX-2 ELISA Kit PicoKine standard curve https://www.bosterbio.com/catalog/product/view/id/1270082026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0421.pngHuman IL-12(P70) PicoKine® Quick ELISA KitHuman IL-12(P70) PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1270092026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0459.pngHuman MMP-2 PicoKine® Quick ELISA KitHuman MMP-2 PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1270102026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0728.pngHuman CXCL5/ENA-78 PicoKine® Quick ELISA KitHuman CXCL5/ENA-78 PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1270112026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0736.pngMouse CXCL10/IP-10 PicoKine® Quick ELISA KitMouse CXCL10/IP-10 PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1270122026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1295.pngRat Angiopoietin-1 PicoKine® Quick ELISA KitRat Angiopoietin-1 PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1270132026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1296.pngMouse Angiopoietin-1 PicoKine® Quick ELISA KitMouse Angiopoietin-1 PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1270142026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0686.pngHuman CCL18/PARC PicoKine® Quick ELISA KitHuman CCL18/PARC PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1270152026-03-10T04:38:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0373.pngHuman IFN Gamma/IFNG/Interferon Gamma PicoKine® Quick ELISA KitHuman IFN Gamma PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-gip-dz41579-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-centromere-protein-t-dz41607-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-chlamydomonas-reinhardtii-crptch1-dz41612-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-unc13b-protein-dz41614-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-liprin-alpha-protein-dz41615-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-fife-dz41616-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-neto-dz41619-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-rim-dz41621-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-stj-dz41622-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-3xflag-dz41623-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-cepn-dz41626-boster.html2026-03-10T04:38:01+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-pmf1-dz41628-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-ska1-dz41629-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-cenpf-dz41630-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-ahtcf1-dz41631-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-nup107-dz41632-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-pcna-dz41633-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-knstrn-dz41635-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-epstein-barr-virus-ebna1-dz41636-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-water-jellyfish-gfp-dz41637-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-mus-musculus-papillomavirus-type-1-e7-boster.html2026-03-10T04:38:02+00:00daily0.9 https://www.bosterbio.com/products/all-recombinant-proteins/human-trance-tnfsf11-rank-l-recombinant-protein-proto14788-5-boster.html2026-03-10T04:38:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto14788-5-sds-page.jpgHuman TRANCE/RANK L/TNFSF11 Recombinant Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto14788-5-biological-activity.jpgHuman TRANCE/RANK L/TNFSF11 Recombinant ProteinHuman TRANCE stimulates osteoclast differentiation in the RAW 264.7 mouse monocyte/macrophage cells. The ED50 range ≤ 25 ng/ml. https://www.bosterbio.com/products/all-recombinant-proteins/human-lilra3-cd85e-recombinant-protein-protoq8n6c8-boster.html2026-03-10T04:38:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protoq8n6c8-sds-page.jpgHuman LILRA3/CD85e Recombinant Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain https://www.bosterbio.com/catalog/product/view/id/1270412026-03-10T04:38:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13232-8-sds-page.jpgHuman IL-7 Recombinant Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stainhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13232-8-bioactivity.jpgHuman IL-7 Recombinant ProteinHuman IL-7 stimulates cell proliferation of the PHA-activated human Peripheral Blood Mononuclear Cells(PBMC). The ED50 range ≤ 8 ng/ml. https://www.bosterbio.com/catalog/product/view/id/1270422026-03-10T04:38:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1270432026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01581-1-bmpr1a-primary-antibodies-wb-testing-1.jpgAnti-BMPR1A Antibody Picoband® Western blot analysis of BMPR1A using anti-BMPR1A antibody (A01581-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BMPR1A antigen affinity purified polyclonal antibody (Catalog # A01581-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BMPR1A at approximately 60 kDa. The expected band size for BMPR1A is at 60 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01581-1-bmpr1a-primary-antibodies-ihc-testing-2.jpgAnti-BMPR1A Antibody Picoband® IHC analysis of BMPR1A using anti-BMPR1A antibody (A01581-1). BMPR1A was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BMPR1A Antibody (A01581-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01581-1-bmpr1a-primary-antibodies-fcm-testing-3.jpgAnti-BMPR1A Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-BMPR1A antibody (A01581-1). Overlay histogram showing MCF-7 cells stained with A01581-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-BMPR1A Antibody (A01581-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270442026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03072-2-bbs1-primary-antibodies-wb-testing-1.jpgAnti-BBS1 Antibody Picoband® Western blot analysis of BBS1 using anti-BBS1 antibody (A03072-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat kidney tissue lysates, Lane 2: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BBS1 antigen affinity purified polyclonal antibody (Catalog # A03072-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BBS1 at approximately 65 kDa. The expected band size for BBS1 is at 65 kDa. https://www.bosterbio.com/catalog/product/view/id/1270452026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-wb-testing-1.jpgAnti-BAP29/BCAP29 Antibody Picoband® Western blot analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HUVEC whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BAP29/BCAP29 antigen affinity purified polyclonal antibody (Catalog # A11769-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BAP29/BCAP29 at approximately 25 kDa. The expected band size for BAP29/BCAP29 is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-ihc-testing-2.jpgAnti-BAP29/BCAP29 Antibody Picoband® IHC analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). BAP29/BCAP29 was detected in a paraffin-embedded section of human colorectal adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP29/BCAP29 Antibody (A11769-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-ihc-testing-3.jpgAnti-BAP29/BCAP29 Antibody Picoband® IHC analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). BAP29/BCAP29 was detected in a paraffin-embedded section of human lung adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP29/BCAP29 Antibody (A11769-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-ihc-testing-4.jpgAnti-BAP29/BCAP29 Antibody Picoband® IHC analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). BAP29/BCAP29 was detected in a paraffin-embedded section of human prostatic acinar adenocarcinoma tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP29/BCAP29 Antibody (A11769-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-ihc-testing-5.jpgAnti-BAP29/BCAP29 Antibody Picoband® IHC analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). BAP29/BCAP29 was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP29/BCAP29 Antibody (A11769-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-ihc-testing-6.jpgAnti-BAP29/BCAP29 Antibody Picoband® IHC analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). BAP29/BCAP29 was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-BAP29/BCAP29 Antibody (A11769-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-if-testing-7.jpgAnti-BAP29/BCAP29 Antibody Picoband® IF analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). BAP29/BCAP29 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BAP29/BCAP29 Antibody (A11769-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-if-testing-1.jpgAnti-BAP29/BCAP29 Antibody Picoband®IF analysis of BAP29/BCAP29 using anti-BAP29/BCAP29 antibody (A11769-1). BAP29/BCAP29 was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-BAP29/BCAP29 Antibody (A11769-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11769-1-bcap29-primary-antibodies-fcm-testing-8.jpgAnti-BAP29/BCAP29 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-BAP29/BCAP29 antibody (A11769-1). Overlay histogram showing A549 cells stained with A11769-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BAP29/BCAP29 Antibody (A11769-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270472026-03-17T05:16:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05302-1-brd1-primary-antibodies-wb-testing-1.jpgAnti-BRD1 Antibody Picoband® Western blot analysis of BRD1 using anti-BRD1 antibody (A05302-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: rat thymus tissue lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BRD1 antigen affinity purified polyclonal antibody (Catalog # A05302-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BRD1 at approximately 120 kDa. The expected band size for BRD1 is at 120 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05302-1-brd1-primary-antibodies-if-testing-2.jpgAnti-BRD1 Antibody Picoband® IF analysis of BRD1 using anti-BRD1 antibody (A05302-1) and anti-Beta Tubulin antibody (M01857-3). BRD1 was detected in immunocytochemical section of HELA cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BRD1 Antibody (A04887-1) and mouse anti-Beta Tubulin antibody (A05302-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05302-1-brd1-primary-antibodies-fcm-testing-3.jpgAnti-BRD1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-BRD1 antibody (A05302-1). Overlay histogram showing SH-SY5Y cells stained with A05302-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BRD1 Antibody (A05302-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270482026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03215-3-myl2-primary-antibodies-wb-testing-1.jpgAnti-Myosin Light Chain 2/MLC-2V/MYL2 Antibody Picoband® Western blot analysis of Myosin Light Chain 2/MLC-2V/MYL2 using anti-Myosin Light Chain 2/MLC-2V/MYL2 antibody (A03215-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: monkey heart tissue lysates, Lane 3: rat heart tissue lysates, Lane 4: rat skeletal muscle tissue lysates, Lane 5: mouse heart tissue lysates, Lane 6: mouse skeletal muscle lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Myosin Light Chain 2/MLC-2V/MYL2 antigen affinity purified polyclonal antibody (Catalog # A03215-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Myosin Light Chain 2/MLC-2V/MYL2 at approximately 19 kDa. The expected band size for Myosin Light Chain 2/MLC-2V/MYL2 is at 19 kDa. https://www.bosterbio.com/catalog/product/view/id/1270492026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04730-2-myl3-primary-antibodies-wb-testing-1.jpgAnti-MYL3 Antibody Picoband® Western blot analysis of MYL3 using anti-MYL3 antibody (A04730-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human H9C2(2-1) whole cell lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse skeletal muscle tissue lysates, Lane 6: mouse C2C12 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYL3 antigen affinity purified polyclonal antibody (Catalog # A04730-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYL3 at approximately 25 kDa. The expected band size for MYL3 is at 22 kDa. https://www.bosterbio.com/catalog/product/view/id/1270502026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08496-2-myl4-primary-antibodies-wb-testing-1.jpgAnti-MYL4 Antibody Picoband® Western blot analysis of MYL4 using anti-MYL4 antibody (A08496-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYL4 antigen affinity purified polyclonal antibody (Catalog # A08496-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYL4 at approximately 24 kDa. The expected band size for MYL4 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08496-2-myl4-primary-antibodies-wb-testing-2.jpgAnti-MYL4 Antibody Picoband® Western blot analysis of MYL4 using anti-MYL4 antibody (A08496-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: rat heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYL4 antigen affinity purified polyclonal antibody (Catalog # A08496-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYL4 at approximately 24 kDa. The expected band size for MYL4 is at 22 kDa. https://www.bosterbio.com/catalog/product/view/id/1270512026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09646-1-myl6-primary-antibodies-wb-testing-1.jpgAnti-MYL6 Antibody Picoband® Western blot analysis of MYL6 using anti-MYL6 antibody (A09646-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYL6 antigen affinity purified polyclonal antibody (Catalog # A09646-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MYL6 at approximately 16 kDa. The expected band size for MYL6 is at 16 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09646-1-myl6-primary-antibodies-fcm-testing-2.jpgAnti-MYL6 Antibody Picoband® Flow Cytometry analysis of Hela cells using anti-MYL6 antibody (A09646-1). Overlay histogram showing Hela cells stained with A09646-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYL6 Antibody (A09646-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270522026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02665-3-atp6ap2-primary-antibodies-wb-testing-1.jpgAnti-Renin receptor/ATP6AP2 Antibody Picoband® Western blot analysis of Renin receptor/ATP6AP2 using anti-Renin receptor/ATP6AP2 antibody (A02665-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human HUVEC whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Renin receptor/ATP6AP2 antigen affinity purified polyclonal antibody (Catalog # A02665-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Renin receptor/ATP6AP2 at approximately 49 kDa. The expected band size for Renin receptor/ATP6AP2 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02665-3-atp6ap2-primary-antibodies-if-testing-2.jpgAnti-Renin receptor/ATP6AP2 Antibody Picoband® IF analysis of Renin receptor/ATP6AP2 using anti-Renin receptor/ATP6AP2 antibody (A02665-3). Renin receptor/ATP6AP2 was detected in an immunocytochemical section of HELA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Renin receptor/ATP6AP2 Antibody (A02665-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02665-3-atp6ap2-primary-antibodies-fcm-testing-3.jpgAnti-Renin receptor/ATP6AP2 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Renin receptor/ATP6AP2 antibody (A02665-3). Overlay histogram showing SiHa cells stained with A02665-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Renin receptor/ATP6AP2 Antibody (A02665-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02665-3-atp6ap2-primary-antibodies-ip-testing-4.jpgAnti-Renin receptor/ATP6AP2 Antibody Picoband® Immunoprecipitating Renin receptor/ATP6AP2 in U251 whole cell lysate. Western blot analysis of Renin receptor/ATP6AP2 using anti-Renin receptor/ATP6AP2 antibody (A02665-3); Lane 1: U251 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-Renin receptor/ATP6AP2 antibody in U251 whole cell lysate; Lane 3: anti-Renin receptor/ATP6AP2 antibody (2μg) + U251 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-Renin receptor/ATP6AP2 antigen affinity purified polyclonal antibody (A02665-3) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for Renin receptor/ATP6AP2 at approximately 45 kDa. The expected band size for Renin receptor/ATP6AP2 is at 39 kDa. https://www.bosterbio.com/catalog/product/view/id/1270532026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03107-3-bnip3l-primary-antibodies-wb-testing-1.jpgAnti-BNIP3L Antibody Picoband® Western blot analysis of BNIP3L using anti-BNIP3L antibody (A03107-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BNIP3L antigen affinity purified polyclonal antibody (Catalog # A03107-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BNIP3L at approximately 35 kDa. The expected band size for BNIP3L is at 24 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03107-3-bnip3l-primary-antibodies-if-testing-2.jpgAnti-BNIP3L Antibody Picoband® IF analysis of BNIP3L using anti-BNIP3L antibody (A03107-3). BNIP3L was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BNIP3L Antibody (A03107-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03107-3-bnip3l-primary-antibodies-fcm-testing-3.jpgAnti-BNIP3L Antibody Picoband® Flow Cytometry analysis of JK cells using anti-BNIP3L antibody (A03107-3). Overlay histogram showing JK cells stained with A03107-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BNIP3L Antibody (A03107-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270542026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-rab27b-primary-antibodies-wb-testing-1.jpgAnti-RAB27B Antibody Picoband® Western blot analysis of RAB27B using anti-RAB27B antibody (A04890-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human U-87MG whole cell lysates, Lane 4: rat stomach tissue lysates, Lane 5: mouse stomach tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-RAB27B antigen affinity purified polyclonal antibody (Catalog # A04890-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for RAB27B at approximately 25 kDa. The expected band size for RAB27B is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-1-s2.0-s2590006425008841-gr2.jpgAnti-RAB27B Antibody Picoband®CircPUM1 promotes angiogenesis in ovarian cancer as the form of exosomes. (A) The expression of circPUM1 was positively related with MVD in ovarian cancer tissue. (B) Experimental design schematic (Created in BioRender. Guan, X. (2025) https://BioRender.com/f5br0q0): HUVEC were co-cultured with exosomes derived from circPUM1-overexpressing and control OVCAR3 cells. (C) RT-qPCR showed that circPUM1 was highly expressed in HUVEC after co-cultured with exosomal circPUM1. Exosomal circPUM1 enhanced migration ability (D, E), viability (F), invasiveness (G), and tube formation ability (H) of HUVECs. (I) Circular RNA pull-down assays using biotinylated circPUM1 probes confirmed co-enrichment of circPUM1 and miR-607. (J) Dual-luciferase reporter assays showed miR-607 targeting 3′-UTR in both VEGFA and RAB27B. (K) Western blot revealed that overexpression of circPUM1 upregulated VEGFA and RAB27B, whereas miR-607 downregulated these targets in OVCAR3 cells. Exosomal circPUM1 elevated intracellular VEGFA expression in HUVECs. (L) Molecular schematic (Created in BioRender. Guan, X. (2025) https://BioRender.com/5eldsz5): In ovarian cancer, the highly expressed circPUM1 sponges miR-607, upregulating expression of VEGFA and RAB27B. This dual regulation establishes a pro-tumorigenic cascade through two distinct pathways: (1) RAB27B-mediated secretion of exosomal circPUM1, and (2) VEGFA-induced activation of angiogenic signaling. Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2590006425008841'>41050095</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-1-s2.0-s2590006425008841-gr4.jpgAnti-RAB27B Antibody Picoband®In vitro antitumor performance of P-Nb2C@si-circPUM1 in ovarian cancer cells. (A) Confocal microscopy images showed intracellular uptake of Cy3-labeled circPUM1 siRNA. Cell apoptosis assays (B), Transwell assays (C), wound healing assays (E) and EdU proliferation assays (F) showed that P-Nb2C-loaded circPUM1 siRNA effectively suppressed ovarian cancer cell phenotypes. (G) RT-qPCR demonstrated a significant downregulation of circPUM1 expression in lipo2000-transfected and P-Nb2C-loaded siRNA groups. Immunofluorescence (D) and Western blot (H) validated the downregulation of VEGFA and RAB27B expression in cells treated with P-Nb2C@si-circPUM1. (I) CCK8 assays showed inhibition of ovarian cancer cell viability in lipo2000-transfected and P-Nb2C-loaded siRNA groups. Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2590006425008841'>41050095</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-1-s2.0-s2590006425008841-gr7.jpgAnti-RAB27B Antibody Picoband®Molecular mechanism validation of P-Nb2C-PEG@si-circPUM1 anti-angiogenic performance in vivo. (A) H&E staining showed increased necrotic loci within tumors of P-Nb2C-PEG@si-circPUM1 group. (B, D) IHC staining of Ki-67 demonstrated a clear reduction in Ki-67-positive cells in P-Nb2C-PEG@si-circPUM1 group. (C, F) IHC staining of CD31 indicated a marked decrease in MVD within tumors of P-Nb2C-PEG@si-circPUM1 group. (H) QPCR showed a significant downregulation of circPUM1 expression in the P-Nb2C-PEG@si-circPUM1 treated group. IHC (E, G) and Western blot (I, J) demonstrated significant down-regulation of RAB27B and VEGFA. Index in PubMed under a CC BY license. PMID: <a href='https://www.sciencedirect.com/science/article/pii/S2590006425008841'>41050095</a>https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-rab27b-primary-antibodies-ihc-testing-2.jpgAnti-RAB27B Antibody Picoband® IHC analysis of RAB27B using anti-RAB27B antibody (A04890-1). RAB27B was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB27B Antibody (A04890-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-rab27b-primary-antibodies-ihc-testing-3.jpgAnti-RAB27B Antibody Picoband® IHC analysis of RAB27B using anti-RAB27B antibody (A04890-1). RAB27B was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB27B Antibody (A04890-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-rab27b-primary-antibodies-ihc-testing-4.jpgAnti-RAB27B Antibody Picoband® IHC analysis of RAB27B using anti-RAB27B antibody (A04890-1). RAB27B was detected in a paraffin-embedded section of mouse stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB27B Antibody (A04890-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-rab27b-primary-antibodies-ihc-testing-5.jpgAnti-RAB27B Antibody Picoband® IHC analysis of RAB27B using anti-RAB27B antibody (A04890-1). RAB27B was detected in a paraffin-embedded section of rat stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-RAB27B Antibody (A04890-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-rab27b-primary-antibodies-if-testing-6.jpgAnti-RAB27B Antibody Picoband® IF analysis of RAB27B using anti-RAB27B antibody (A04890-1). RAB27B was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-RAB27B Antibody (A04890-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04890-1-rab27b-primary-antibodies-fcm-testing-7.jpgAnti-RAB27B Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-RAB27B antibody (A04890-1). Overlay histogram showing PC-3 cells stained with A04890-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-RAB27B Antibody (A04890-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270552026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a34011-bcar4-primary-antibodies-wb-testing-1.jpgAnti-BCAR4 Antibody Picoband® Western blot analysis of BCAR4 using anti-BCAR4 antibody (A34011). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat C6 whole cell lysates, Lane 2: rat PC-12 whole cell lysates, Lane 3: rat RH35 whole cell lysates, Lane 4:mouse RAW265.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BCAR4 antigen affinity purified polyclonal antibody (Catalog # A34011) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for BCAR4 at approximately 13 kDa. The expected band size for BCAR4 is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a34011-bcar4-primary-antibodies-fcm-testing-2.jpgAnti-BCAR4 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-BCAR4 antibody (A34011). Overlay histogram showing 293T cells stained with A34011 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-BCAR4 Antibody (A34011, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270562026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13797-1-wdr55-primary-antibodies-wb-testing-1.jpgAnti-WDR55 Antibody Picoband® Western blot analysis of WDR55 using anti-WDR55 antibody (A13797-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-WDR55 antigen affinity purified polyclonal antibody (Catalog # A13797-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for WDR55 at approximately 50 kDa. The expected band size for WDR55 is at 42 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13797-1-wdr55-primary-antibodies-fcm-testing-2.jpgAnti-WDR55 Antibody Picoband® Flow Cytometry analysis of JK cells using anti-WDR55 antibody (A13797-1). Overlay histogram showing JK cells stained with A13797-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-WDR55 Antibody (A13797-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270572026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00739-1-cga-primary-antibodies-wb-testing-1.jpgAnti-Chromogranin A/CGA Antibody Picoband® Western blot analysis of Chromogranin A/CGA using anti-Chromogranin A/CGA antibody (A00739-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Chromogranin A/CGA antigen affinity purified polyclonal antibody (Catalog # A00739-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Chromogranin A/CGA at approximately 17 kDa. The expected band size for Chromogranin A/CGA is at 13 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00739-1-cga-primary-antibodies-ihc-testing-2.jpgAnti-Chromogranin A/CGA Antibody Picoband® IHC analysis of Chromogranin A/CGA using anti-Chromogranin A/CGA antibody (A00739-1). Chromogranin A/CGA was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Chromogranin A/CGA Antibody (A00739-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00739-1-cga-primary-antibodies-fcm-testing-3_1.jpgAnti-Chromogranin A/CGA Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-Chromogranin A/CGA antibody (A00739-1). Overlay histogram showing 293T cells stained with A00739-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Chromogranin A/CGA Antibody (A00739-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270582026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01706-2-ncoa2-primary-antibodies-wb-testing-1_1.jpgAnti-NCOA2 Antibody Picoband® Western blot analysis of NCOA2 using anti-NCOA2 antibody (A01706-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NCOA2 antigen affinity purified polyclonal antibody (A01706-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054) at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NCOA2 at approximately 160-170 kDa. The expected band size for NCOA2 is at 159 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01706-2-ncoa2-primary-antibodies-ihc-testing-2_1.jpgAnti-NCOA2 Antibody Picoband® IHC analysis of NCOA2 using anti-NCOA2 antibody (A01706-2). NCOA2 was detected in a paraffin-embedded section of human prostate hyperplasia cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCOA2 Antibody (A01706-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01706-2-ncoa2-primary-antibodies-ihc-testing-3.jpgAnti-NCOA2 Antibody Picoband® IHC analysis of NCOA2 using anti-NCOA2 antibody (A01706-2). NCOA2 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NCOA2 Antibody (A01706-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01706-2-ncoa2-primary-antibodies-if-testing-4.jpgAnti-NCOA2 Antibody Picoband® IF analysis of NCOA2 using anti-NCOA2 antibody (A01706-2) and anti-Tubulin Alpha antibody (M03989-3). NCOA2 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NCOA2 Antibody (A01706-2) and mouse anti-Tubulin Alpha antibody (M03989-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01706-2-ncoa2-primary-antibodies-fcm-testing-5.jpgAnti-NCOA2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-NCOA2 antibody (A01706-2). Overlay histogram showing MCF-7 cells stained with A01706-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NCOA2 Antibody (A01706-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270592026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01125-3-chd4-primary-antibodies-wb-testing-1.jpgAnti-CHD4 Antibody Picoband® Western blot analysis of CHD4 using anti-CHD4 antibody (A01125-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U20S whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHD4 antigen affinity purified polyclonal antibody (Catalog # A01125-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHD4 at approximately 260 kDa. The expected band size for CHD4 is at 218 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01125-3-chd4-primary-antibodies-fcm-testing-2.jpgAnti-CHD4 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-CHD4 antibody (A01125-3). Overlay histogram showing MCF-7 cells stained with A01125-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHD4 Antibody (A01125-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270602026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a16012-1-stox2-primary-antibodies-wb-testing-1.jpgAnti-STOX2 Antibody Picoband® Western blot analysis of STOX2 using anti-STOX2 antibody (A16012-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human RT4 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-STOX2 antigen affinity purified polyclonal antibody (Catalog # A16012-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for STOX2 at approximately 102 kDa. The expected band size for STOX2 is at 102 kDa. https://www.bosterbio.com/catalog/product/view/id/1270612026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08381-1-cldn11-primary-antibodies-wb-testing-1.jpgAnti-CLDN11 Antibody Picoband® Western blot analysis of CLDN11 using anti-CLDN11 antibody (A08381-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HUVEC whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLDN11 antigen affinity purified polyclonal antibody (Catalog # A08381-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CLDN11 at approximately 22 kDa. The expected band size for CLDN11 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08381-1-cldn11-primary-antibodies-fcm-testing-2.jpgAnti-CLDN11 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-CLDN11 antibody (A08381-1). Overlay histogram showing HepG2 cells stained with A08381-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-CLDN11 Antibody (A08381-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270622026-03-17T05:16:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09071-1-cltb-primary-antibodies-wb-testing-1.jpgAnti-CLTB Antibody Picoband® Western blot analysis of CLTB using anti-CLTB antibody (A09071-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: rat thymus tissue lysates, Lane 5: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CLTB antigen affinity purified polyclonal antibody (Catalog # A09071-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CLTB at approximately 32 kDa. The expected band size for CLTB is at 25 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09071-1-cltb-primary-antibodies-ihc-testing-2.jpgAnti-CLTB Antibody Picoband® IHC analysis of CLTB using anti-CLTB antibody (A09071-1). CLTB was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLTB Antibody (A09071-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09071-1-cltb-primary-antibodies-ihc-testing-3.jpgAnti-CLTB Antibody Picoband® IHC analysis of CLTB using anti-CLTB antibody (A09071-1). CLTB was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLTB Antibody (A09071-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09071-1-cltb-primary-antibodies-ihc-testing-4.jpgAnti-CLTB Antibody Picoband® IHC analysis of CLTB using anti-CLTB antibody (A09071-1). CLTB was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLTB Antibody (A09071-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09071-1-cltb-primary-antibodies-ihc-testing-5.jpgAnti-CLTB Antibody Picoband® IHC analysis of CLTB using anti-CLTB antibody (A09071-1). CLTB was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CLTB Antibody (A09071-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09071-1-cltb-primary-antibodies-fcm-testing-6.jpgAnti-CLTB Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-CLTB antibody (A09071-1). Overlay histogram showing A431 cells stained with A09071-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CLTB Antibody (A09071-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270632026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03299-1-cdkn2c-primary-antibodies-wb-testing-1.jpgAnti-CDKN2C Antibody Picoband® Western blot analysis of CDKN2C using anti-CDKN2C antibody (A03299-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDKN2C antigen affinity purified polyclonal antibody (Catalog # A03299-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDKN2C at approximately 18 kDa. The expected band size for CDKN2C is at 18 kDa. https://www.bosterbio.com/catalog/product/view/id/1270642026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-wb-testing-1.jpgAnti-YWHAH Antibody Picoband® Western blot analysis of YWHAH using anti-YWHAH antibody (A04219-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: monkey COS-7 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-YWHAH antigen affinity purified polyclonal antibody (Catalog # A04219-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for YWHAH at approximately 28 kDa. The expected band size for YWHAH is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-ihc-testing-2.jpgAnti-YWHAH Antibody Picoband® IHC analysis of YWHAH using anti-YWHAH antibody (A04219-2). YWHAH was detected in a paraffin-embedded section of mouse cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YWHAH Antibody (A04219-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-ihc-testing-4.jpgAnti-YWHAH Antibody Picoband®IHC analysis of YWHAH using anti-YWHAH antibody (A04219-2). YWHAH was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YWHAH Antibody (A04219-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-ihc-testing-5.jpgAnti-YWHAH Antibody Picoband®IHC analysis of YWHAH using anti-YWHAH antibody (A04219-2). YWHAH was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YWHAH Antibody (A04219-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-ihc-testing-3.jpgAnti-YWHAH Antibody Picoband® IHC analysis of YWHAH using anti-YWHAH antibody (A04219-2). YWHAH was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-YWHAH Antibody (A04219-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-if-testing-4.jpgAnti-YWHAH Antibody Picoband® IF analysis of YWHAH using anti-YWHAH antibody (A04219-2). YWHAH was detected in an immunocytochemical section of U20S cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-YWHAH Antibody (A04219-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-if-testing-1.jpgAnti-YWHAH Antibody Picoband®IF analysis of YWHAH using anti-YWHAH antibody (A04219-2). YWHAH was detected in a paraffin-embedded section of rat cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 5 μg/mL rabbit anti-YWHAH Antibody (A04219-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04219-2-ywhah-primary-antibodies-fcm-testing-5.jpgAnti-YWHAH Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-YWHAH antibody (A04219-2). Overlay histogram showing 293T cells stained with A04219-2(Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-YWHAH Antibody (A04219-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270652026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11201-2-synpr-primary-antibodies-wb-testing-1.jpgAnti-Synaptoporin/SYNPR Antibody Picoband® Western blot analysis of Synaptoporin/SYNPR using anti-Synaptoporin/SYNPR antibody (A11201-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Synaptoporin/SYNPR antigen affinity purified polyclonal antibody (Catalog # A11201-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Synaptoporin/SYNPR at approximately 37 kDa. The expected band size for Synaptoporin/SYNPR is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11201-2-synpr-primary-antibodies-ihc-testing-2.jpgAnti-Synaptoporin/SYNPR Antibody Picoband® IHC analysis of Synaptoporin/SYNPR using anti-Synaptoporin/SYNPR antibody (A11201-2). Synaptoporin/SYNPR was detected in a paraffin-embedded section of mouse brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Synaptoporin/SYNPR Antibody (A11201-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11201-2-synpr-primary-antibodies-ihc-testing-3.jpgAnti-Synaptoporin/SYNPR Antibody Picoband® IHC analysis of Synaptoporin/SYNPR using anti-Synaptoporin/SYNPR antibody (A11201-2). Synaptoporin/SYNPR was detected in a paraffin-embedded section of rat brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Synaptoporin/SYNPR Antibody (A11201-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11201-2-synpr-primary-antibodies-fcm-testing-4.jpgAnti-Synaptoporin/SYNPR Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-Synaptoporin/SYNPR antibody (A11201-2). Overlay histogram showing HepG2 cells stained with A11201-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Synaptoporin/SYNPR Antibody (A11201-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270662026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13211-2-meiob-primary-antibodies-wb-testing-1.jpgAnti-MEIOB Antibody Picoband® Western blot analysis of MEIOB using anti-MEIOB antibody (A13211-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MEIOB antigen affinity purified polyclonal antibody (Catalog # A13211-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MEIOB at approximately 49 kDa. The expected band size for MEIOB is at 49 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13211-2-meiob-primary-antibodies-if-testing-2.jpgAnti-MEIOB Antibody Picoband® IF analysis of MEIOB using anti-MEIOB antibody (A13211-2). MEIOB was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MEIOB Antibody (A13211-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13211-2-meiob-primary-antibodies-fcm-testing-3.jpgAnti-MEIOB Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-MEIOB antibody (A13211-2). Overlay histogram showing K562 cells stained with A13211-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MEIOB Antibody (A13211-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270672026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10929-2-nek11-primary-antibodies-wb-testing-1.jpgAnti-NEK11 Antibody Picoband® Western blot analysis of NEK11 using anti-NEK11 antibody (A10929-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat C6 whole cell lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NEK11 antigen affinity purified polyclonal antibody (Catalog # A10929-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NEK11 at approximately 74 kDa. The expected band size for NEK11 is at 74 kDa. https://www.bosterbio.com/catalog/product/view/id/1270682026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11992-1-mbtd1-primary-antibodies-wb-testing-1.jpgAnti-MBTD1 Antibody Picoband® Western blot analysis of MBTD1 using anti-MBTD1 antibody (A11992-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MBTD1 antigen affinity purified polyclonal antibody (Catalog # A11992-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MBTD1 at approximately 71 kDa. The expected band size for MBTD1 is at 71 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11992-1-mbtd1-primary-antibodies-if-testing-2.jpgAnti-MBTD1 Antibody Picoband® IF analysis of MBTD1 using anti-MBTD1 antibody (A11992-1) and anti-Beta Tubulin antibody (M01857-3). MBTD1 was detected in immunocytochemical section of U2OS cell. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-MBTD1 Antibody (A11992-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11992-1-mbtd1-primary-antibodies-fcm-testing-3.jpgAnti-MBTD1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-MBTD1 antibody (A11992-1). Overlay histogram showing SH-SY5Y cells stained with A11992-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MBTD1 Antibody (A11992-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270692026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07226-1-mcm9-primary-antibodies-wb-testing-1.jpgAnti-MCM9 Antibody Picoband® Western blot analysis of MCM9 using anti-MCM9 antibody (A07226-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCM9 antigen affinity purified polyclonal antibody (Catalog # A07226-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MCM9 at approximately 127 kDa. The expected band size for MCM9 is at 127 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07226-1-mcm9-primary-antibodies-fcm-testing-2.jpgAnti-MCM9 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-MCM9 antibody (A07226-1). Overlay histogram showing MCF-7 cells stained with A07226-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MCM9 Antibody (A07226-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270702026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15877-1-mettl11b-primary-antibodies-wb-testing-1.jpgAnti-NTMT2 Antibody Picoband® Western blot analysis of NTMT2 using anti-NTMT2 antibody (A15877-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat heart tissue lysates, Lane 3: rat C6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NTMT2 antigen affinity purified polyclonal antibody (Catalog # A15877-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NTMT2 at approximately 32 kDa. The expected band size for NTMT2 is at 32 kDa. https://www.bosterbio.com/catalog/product/view/id/1270712026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01878-4-oas2-primary-antibodies-wb-testing-1.jpgAnti-OAS2 Antibody Picoband® Western blot analysis of OAS2 using anti-OAS2 antibody (A01878-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OAS2 antigen affinity purified polyclonal antibody (Catalog # A01878-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OAS2 at approximately 69 kDa. The expected band size for OAS2 is at 82 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01878-4-oas2-primary-antibodies-fcm-testing-2.jpgAnti-OAS2 Antibody Picoband® Flow Cytometry analysis of Raw264.7 cells using anti-OAS2 antibody (A01878-4). Overlay histogram showing Raw264.7 cells stained with A01878-4 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-OAS2 Antibody (A01878-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1270722026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1270742026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1270752026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1270762026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1270772026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1270782026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1270792026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1270812026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1270822026-03-10T04:38:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1270832026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1270842026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1270852026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1270862026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Colon: transverse https://www.bosterbio.com/catalog/product/view/id/1270872026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1270882026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1270892026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1270902026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1270912026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1270922026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1270932026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1270942026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1270952026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1270962026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1270972026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1270982026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1270992026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271002026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271012026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271022026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271032026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Colon: rectosigmoid https://www.bosterbio.com/catalog/product/view/id/1271042026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1271052026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1271062026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1271072026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271082026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1271092026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1271102026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1271112026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271122026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271132026-03-10T04:38:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1271142026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast, left https://www.bosterbio.com/catalog/product/view/id/1271152026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271162026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271172026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1271182026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1271192026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271202026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271212026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271222026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1271232026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1271242026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271252026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1271262026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Colon: sigmoid https://www.bosterbio.com/catalog/product/view/id/1271272026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1271282026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1271292026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1271302026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271312026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1271322026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1271332026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1271342026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271352026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271372026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271382026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1271392026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1271402026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Colon: sigmoid https://www.bosterbio.com/catalog/product/view/id/1271412026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271422026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1271432026-03-10T04:38:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271442026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1271452026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271462026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1271472026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1271482026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1271492026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1271502026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271512026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1271522026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1271532026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1271542026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1271552026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1271562026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1271572026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1271582026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1271592026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1271602026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1271612026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Small intestine https://www.bosterbio.com/catalog/product/view/id/1271622026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1271632026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1271652026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1271662026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271672026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Gastroesophageal junction https://www.bosterbio.com/catalog/product/view/id/1271682026-03-10T04:38:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271692026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1271702026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271712026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Thyroid gland https://www.bosterbio.com/catalog/product/view/id/1271722026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1271732026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1271742026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1271752026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Thyroid gland https://www.bosterbio.com/catalog/product/view/id/1271762026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1271772026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271782026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1271792026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1271802026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1271812026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271822026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271832026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271842026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271852026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271862026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1271872026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271882026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Jejunum https://www.bosterbio.com/catalog/product/view/id/1271892026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271902026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271912026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1271922026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1271932026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1271942026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271952026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271962026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1271972026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271982026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1271992026-03-10T04:38:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1272002026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1272012026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1272022026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1272032026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272042026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272052026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Gastroesophageal junction https://www.bosterbio.com/catalog/product/view/id/1272062026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272082026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1272092026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1272102026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1272112026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1272122026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272132026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272142026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272152026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1272162026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Urinary bladder https://www.bosterbio.com/catalog/product/view/id/1272172026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272182026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1272192026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Thyroid gland https://www.bosterbio.com/catalog/product/view/id/1272202026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272212026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272222026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272232026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1272242026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1272252026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272262026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1272272026-03-10T04:38:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1272282026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272292026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272302026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272312026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1272322026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272332026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Urinary bladder https://www.bosterbio.com/catalog/product/view/id/1272342026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272352026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272362026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272382026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272392026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1272402026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272412026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272422026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1272432026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1272442026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272452026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272462026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272472026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272482026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1272492026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1272502026-03-10T04:38:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272512026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272522026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272532026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272542026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1272552026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272562026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1272572026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Uterus https://www.bosterbio.com/catalog/product/view/id/1272582026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272592026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272602026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1272612026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1272622026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272632026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1272642026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272652026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272662026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1272672026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272682026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Thyroid gland https://www.bosterbio.com/catalog/product/view/id/1272692026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272702026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_1.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272712026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272722026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1272732026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272752026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272762026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272772026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Small intestine https://www.bosterbio.com/catalog/product/view/id/1272782026-03-10T04:38:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1272792026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272802026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1272812026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon: sigmoid https://www.bosterbio.com/catalog/product/view/id/1272822026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1272832026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Synovium https://www.bosterbio.com/catalog/product/view/id/1272842026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272852026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272862026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1272872026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1272882026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1272892026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon: sigmoid https://www.bosterbio.com/catalog/product/view/id/1272902026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1272912026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272922026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1272932026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1272942026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272952026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272962026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1272972026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1272982026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1272992026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1273002026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1273022026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1273032026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Small intestine https://www.bosterbio.com/catalog/product/view/id/1273042026-03-10T04:38:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1273052026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1273062026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1273082026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1273092026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273102026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273112026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1273122026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1273132026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273142026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273152026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1273162026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Rectum https://www.bosterbio.com/catalog/product/view/id/1273172026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung: left upper lobe https://www.bosterbio.com/catalog/product/view/id/1273182026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1273192026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1273202026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1273212026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273222026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273232026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273242026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon: sigmoid https://www.bosterbio.com/catalog/product/view/id/1273252026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1273262026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1273282026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1273292026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lymph node https://www.bosterbio.com/catalog/product/view/id/1273302026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1273312026-03-10T04:38:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1273322026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273332026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1273342026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273352026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1273362026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1273372026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Synovium https://www.bosterbio.com/catalog/product/view/id/1273382026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1273392026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1273402026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1273412026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung: right lower lobe https://www.bosterbio.com/catalog/product/view/id/1273422026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273432026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung: right lower lobe https://www.bosterbio.com/catalog/product/view/id/1273442026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1273452026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lymph node https://www.bosterbio.com/catalog/product/view/id/1273462026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1273472026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273482026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1273492026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Synovium https://www.bosterbio.com/catalog/product/view/id/1273502026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273512026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273522026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273532026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1273542026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273552026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273562026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1273572026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1273582026-03-10T04:38:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1273592026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273602026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1273612026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273632026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273642026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273652026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273662026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1273672026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1273682026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273692026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1273702026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_2.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1273712026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273722026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273732026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Foreskin https://www.bosterbio.com/catalog/product/view/id/1273742026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273752026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273772026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1273782026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1273792026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymph node https://www.bosterbio.com/catalog/product/view/id/1273802026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1273812026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1273822026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1273832026-03-10T04:38:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273842026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1273852026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1273862026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1273872026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1273882026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1273892026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1273902026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1273912026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273922026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273932026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273942026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1273952026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1273962026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1273972026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1273982026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1273992026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274002026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274012026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1274022026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1274032026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274042026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274052026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1274062026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274072026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1274082026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274092026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274102026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274112026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274122026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274132026-03-10T04:38:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274142026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Synovium https://www.bosterbio.com/catalog/product/view/id/1274152026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274162026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Artery: peripheral https://www.bosterbio.com/catalog/product/view/id/1274172026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274182026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1274192026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274202026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: bilateral https://www.bosterbio.com/catalog/product/view/id/1274212026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1274222026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary https://www.bosterbio.com/catalog/product/view/id/1274232026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1274242026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Synovium https://www.bosterbio.com/catalog/product/view/id/1274252026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1274262026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: left https://www.bosterbio.com/catalog/product/view/id/1274272026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274282026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymph node https://www.bosterbio.com/catalog/product/view/id/1274292026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1274302026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Esophagus https://www.bosterbio.com/catalog/product/view/id/1274312026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Neck https://www.bosterbio.com/catalog/product/view/id/1274322026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274332026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Ovary: right https://www.bosterbio.com/catalog/product/view/id/1274342026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274352026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274362026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274382026-03-10T04:38:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lung https://www.bosterbio.com/catalog/product/view/id/1274392026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1274402026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Colon https://www.bosterbio.com/catalog/product/view/id/1274412026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274422026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274432026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274442026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Lymphoid tissue https://www.bosterbio.com/catalog/product/view/id/1274452026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274462026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Colon: sigmoid https://www.bosterbio.com/catalog/product/view/id/1274472026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274482026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1274492026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274502026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1274512026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274522026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1274532026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274542026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1274552026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274562026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274572026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1274582026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1274592026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274602026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1274612026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274622026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1274632026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1274642026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1274652026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1274662026-03-10T04:38:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1274672026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274692026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274702026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_3.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1274712026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1274722026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1274732026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274742026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274752026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1274762026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274772026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274782026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1274792026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274802026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274812026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1274822026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274832026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274842026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274852026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274862026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1274872026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274882026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Colon: sigmoid https://www.bosterbio.com/catalog/product/view/id/1274892026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Spleen https://www.bosterbio.com/catalog/product/view/id/1274902026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1274912026-03-10T04:38:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274922026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1274932026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1274942026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274952026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1274962026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1274972026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1274982026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1274992026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1275002026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1275012026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1275022026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1275032026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1275042026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1275052026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Colon: rectosigmoid https://www.bosterbio.com/catalog/product/view/id/1275062026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1275072026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1275082026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1275092026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Skin https://www.bosterbio.com/catalog/product/view/id/1275102026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1275112026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Neck https://www.bosterbio.com/catalog/product/view/id/1275122026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Colon: right https://www.bosterbio.com/catalog/product/view/id/1275132026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1275142026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1275152026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1275162026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Kidney https://www.bosterbio.com/catalog/product/view/id/1275172026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Pancreas https://www.bosterbio.com/catalog/product/view/id/1275182026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1275192026-03-10T04:38:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Stomach https://www.bosterbio.com/catalog/product/view/id/1275202026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Liver https://www.bosterbio.com/catalog/product/view/id/1275212026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Colon: rectosigmoid https://www.bosterbio.com/catalog/product/view/id/1275222026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Breast https://www.bosterbio.com/catalog/product/view/id/1275232026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Breast, left https://www.bosterbio.com/catalog/product/view/id/1275242026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/t/i/tissue-protein-lysate_4.jpgTissue Protein Lysate, Prostate https://www.bosterbio.com/catalog/product/view/id/1275252026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0380.pngRat IGF-2 PicoKine® Quick ELISA KitRat IGF-2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275262026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0381_1.pngMouse IGF-2 PicoKine® Quick ELISA KitMouse IGF-2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275272026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1306.pngHuman Cathepsin E PicoKine® Quick ELISA KitHuman Cathepsin E PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275282026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0448.pngHuman MIP-1Alpha/CCL3 PicoKine® Quick ELISA KitHuman CCL3 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275292026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0934.pngHuman ADAM12 PicoKine® Quick ELISA KitHuman ADAM12 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275302026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0557.pngHuman ACE PicoKine® Quick ELISA KitHuman ACE PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275312026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0827.pngHuman RAGE PicoKine® Quick ELISA KitHuman RAGE PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275322026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0371.pngMouse ICAM-1 PicoKine® Quick ELISA KitMouse ICAM-1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275332026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0372.pngRat ICAM-1 PicoKine® Quick ELISA KitRat ICAM-1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275342026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0682.pngHuman CA9 PicoKine® Quick ELISA KitHuman CA9 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275352026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0708.pngMouse CD80/B7-1 PicoKine® Quick ELISA KitMouse B7-1/CD80 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275362026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0912.pngHuman CD23 PicoKine® Quick ELISA KitHuman CD23/FCER2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275372026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0925.pngMouse DKK-1 PicoKine® Quick ELISA KitMouse DKK1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275382026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0939.pngRat CCL4/MIP1Beta PicoKine® Quick ELISA KitRat CCL4/MIP-1 beta PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275392026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1312.pngHuman CD32 PicoKine® Quick ELISA KitHuman CD32/FCGR2b/c PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275402026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1432.pngRat DKK-1 PicoKine® Quick ELISA KitRat DKK1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275412026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0671.pngMouse Cathepsin B PicoKine® Quick ELISA KitMouse Cathepsin B PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275422026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0808.pngMouse CSF1R PicoKine® Quick ELISA KitMouse CSF1R/M-CSFR PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275432026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0574.pngMouse CD40L PicoKine® Quick ELISA KitMouse CD40L PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275442026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0418.pngRat IL-10 PicoKine® Quick ELISA KitRat IL-10 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275452026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1418.pngHuman CD44 PicoKine® Quick ELISA KitHuman CD44 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275462026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0562.pngMouse E-Cadherin PicoKine® Quick ELISA KitMouse E-Cadherin PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275472026-03-10T04:38:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0740.pngMouse CXCL13 PicoKine® Quick ELISA KitMouse CXCL13/BLC PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275482026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0838.pngHuman SMAC PicoKine® Quick ELISA KitHuman SMAC PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275492026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1203.pngHuman CCN1 PicoKine® Quick ELISA KitHuman CCN1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275502026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0679.pngMouse Cystatin C PicoKine® Quick ELISA KitMouse Cystatin C PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275512026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0472.pngHuman Neurotrophin-3/NT-3 PicoKine® Quick ELISA KitHuman Neurotrophin-3 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275522026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0473.pngMouse Neurotrophin-3/NT-3 PicoKine® Quick ELISA KitMouse Neurotrophin-3 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275532026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0474.pngRat Neurotrophin-3/NT-3 PicoKine® Quick ELISA KitRat Neurotrophin-3 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275542026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1433.pngMouse EGFR PicoKine® Quick ELISA KitMouse EGFR PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275552026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0741.pngHuman CXCL16 PicoKine® Quick ELISA KitHuman CXCL16 PicoKine ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-chd1-boster.html2026-03-10T04:38:21+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-tomato-coatomer-subunit-beta-boster.html2026-03-10T04:38:21+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-aqp8a-1-antibody.html2026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/d/z/dz41642-aqp8a.1-primary-antibodies-ihc-testing-1.jpgAnti-Zebrafish aqp8a.1 Antibody IHC analysis of Aqp8a.1 using anti-Aqp8a.1 antibody (DZ41642). Aqp8a.1 was detected in paraffin-embedded section of zebrafish heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Aqp8a.1 Antibody (DZ41642) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-trypanosoma-brucei-brucei-kinetoplast-dna-associated-protein-boster.html2026-03-10T04:38:21+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-appl-boster.html2026-03-10T04:38:21+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-anp32e-antibody.html2026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/d/z/dz41646-anp32e-primary-antibodies-ihc-testing-1.jpgAnti-Zebrafish Anp32e Antibody IHC analysis of Anp32e using anti-Anp32e antibody (DZ41646). Anp32e was detected in paraffin-embedded section of zebrafish brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Anp32e Antibody (DZ41646) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/d/z/dz41646-anp32e-primary-antibodies-ihc-testing-2.jpgAnti-Zebrafish Anp32e Antibody IHC analysis of Anp32e using anti-Anp32e antibody (DZ41646). Anp32e was detected in paraffin-embedded section of zebrafish heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Anp32e Antibody (DZ41646) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/d/z/dz41646-anp32e-primary-antibodies-ihc-testing-3.jpgAnti-Zebrafish Anp32e Antibody IHC analysis of Anp32e using anti-Anp32e antibody (DZ41646). Anp32e was detected in paraffin-embedded section of zebrafish intestines tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Anp32e Antibody (DZ41646) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-fruit-fly-anp32a-boster.html2026-03-10T04:38:21+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-pig-myod1-boster.html2026-03-10T04:38:21+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1275662026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-5-sds-page.jpgAnti-TNFSF2/TNFa Reference Antibody (adalimumab)Anti-TNFSF2 / TNFa Reference Antibody (adalimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-5-sds-page_1.jpgAnti-TNFSF2/TNFa Reference Antibody (adalimumab)Anti-TNFSF2/TNFa Reference Antibody (adalimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-5-sec-hplc_1.jpgAnti-TNFSF2/TNFa Reference Antibody (adalimumab)The purity of Anti-TNFSF2/TNFa Reference Antibody (adalimumab)is more than 98.86%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-5-sec-hplc.jpgAnti-TNFSF2/TNFa Reference Antibody (adalimumab)The purity of Anti-TNFSF2 / TNFa Reference Antibody (adalimumab)is more than 98.86% ,determined by SEC-HPLC. https://www.bosterbio.com/catalog/product/view/id/1275672026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-2-sds-page.jpgAnti-Amyloid Beta Reference Antibody (aducanumab)Anti-Amyloid Beta Reference Antibody (aducanumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-2-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (aducanumab)The purity of Anti-Amyloid Beta Reference Antibody (aducanumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-2-od450.jpgAnti-Amyloid Beta Reference Antibody (aducanumab)Immobilized N His HSA human Amyloid beta(APP) at 2 &mug/mL can bind Anti-Amyloid Beta Reference Antibody (aducanumab) https://www.bosterbio.com/catalog/product/view/id/1275682026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03484-2-sds-page.jpgAnti-CD52 Reference Antibody (alemtuzumab)Anti-CD52 Reference Antibody (alemtuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03484-2-sec-hplc.jpgAnti-CD52 Reference Antibody (alemtuzumab)The purity of Anti-CD52 Reference Antibody (alemtuzumab)is more than 96.85% https://www.bosterbio.com/catalog/product/view/id/1275692026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-3-sds-page.jpgAnti-PCSK9 Reference Antibody (alirocumab)Anti-PCSK9 Reference Antibody (alirocumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-3-sec-hplc.jpgAnti-PCSK9 Reference Antibody (alirocumab)The purity of Anti-PCSK9 Reference Antibody (alirocumab)is more than 96.96%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-3-od450.jpgAnti-PCSK9 Reference Antibody (alirocumab)Immobilized human PCSK9 chis at 2 &mug/mL can bind Anti-PCSK9 Reference Antibody (alirocumab) https://www.bosterbio.com/catalog/product/view/id/1275702026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-6-sds-page.jpgAnti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-6-sec-hplc.jpgAnti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-6-od450.jpgAnti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)Immobilized human PD L1 His at 2 &mug/mL can bind Anti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-6-facs.jpgAnti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)Human PD-L1 CHO-K cells were stained with Anti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-6-killing-rate.jpgAnti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)The endocytosis ratio atezolizumab by HCC827 increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-6-syngeneic-mc38-cell-model.jpgAnti-B7-H1/PD-L1/CD274 Reference Antibody (atezolizumab)Atezolizumab inhibited the tumor growth of MC38 on C57BL/6N mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1275712026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-2-sds-page.jpgAnti-IL-2Ra/CD25 Reference Antibody (basiliximab)Anti-IL-2Ra/CD25 Reference Antibody (basiliximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-2-sec-hplc.jpgAnti-IL-2Ra/CD25 Reference Antibody (basiliximab)The purity of Anti-IL-2Ra/CD25 Reference Antibody (basiliximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1275722026-03-10T04:38:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-5-sds-page.jpgAnti-IL-1b Reference Antibody (canakinumab)Anti-IL-1b Reference Antibody (canakinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-5-sec-hplc.jpgAnti-IL-1b Reference Antibody (canakinumab)The purity of Anti-IL-1b Reference Antibody (canakinumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1275732026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-6-sds-page.jpgAnti-ERBB1/EGFR/HER1 Reference Antibody (cetuximab)Anti-ERBB1/EGFR/HER1 Reference Antibody (cetuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-6-sec-hplc.jpgAnti-ERBB1/EGFR/HER1 Reference Antibody (cetuximab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (cetuximab)is more than 99.92%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-6-facs.jpgAnti-ERBB1/EGFR/HER1 Reference Antibody (cetuximab)Human EGFR CHO-K cells were stained with Anti-ERBB1/EGFR/HER1 Reference Antibody (cetuximab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1275742026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04466-4-sds-page.jpgAnti-Integrin aL/ITGAL/CD11a Reference Antibody (efalizumab)Anti-Integrin aL/ITGAL/CD11a Reference Antibody (efalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04466-4-sec-hplc.jpgAnti-Integrin aL/ITGAL/CD11a Reference Antibody (efalizumab)The purity of Anti-Integrin aL/ITGAL/CD11a Reference Antibody (efalizumab)is more than 98.77% https://www.bosterbio.com/catalog/product/view/id/1275752026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-3-sds-page.jpgAnti-Siglec-3/CD33 Reference Antibody (Gemtuzumab)Anti-Siglec-3/CD33 Reference Antibody (Gemtuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-3-sec-hplc.jpgAnti-Siglec-3/CD33 Reference Antibody (Gemtuzumab)The purity of Anti-Siglec-3/CD33 Reference Antibody (Gemtuzumab)is more than 99.54%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-3-od450.jpgAnti-Siglec-3/CD33 Reference Antibody (Gemtuzumab)Immobilized human CD33 His at 2 &mug/mL can bind Anti-Siglec-3/CD33 Reference Antibody (Gemtuzumab) https://www.bosterbio.com/catalog/product/view/id/1275762026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-1-sds-page.jpgAnti-IL-5 Reference Antibody (mepolizumab)Anti-IL-5 Reference Antibody (mepolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-1-sec-hplc.jpgAnti-IL-5 Reference Antibody (mepolizumab)The purity of Anti-IL-5 Reference Antibody (mepolizumab)is more than 98.47%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-1-od450.jpgAnti-IL-5 Reference Antibody (mepolizumab)Immobilized human IL 5 His at 2 &mug/mL can bind Anti-IL-5 Reference Antibody (mepolizumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-1-facs.jpgAnti-IL-5 Reference Antibody (mepolizumab)Anti-IL-5 Reference Antibody (mepolizumab) FACS Blocking was evaluated using Human IL-5Rbeta-FL/HIL-5Ralpha CHOS. The IC50 was approximately 2.844 ug/mL.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-1-facs-1.jpgAnti-IL-5 Reference Antibody (mepolizumab)Mepolizumab induced proliferation inhibition activity was evaluated using Human IL-5Ralpha TF-1 . The EC50 was approximately 0.3282 ug/mL. https://www.bosterbio.com/catalog/product/view/id/1275772026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-2-sds-page.jpgAnti-Integrin a4/ITGA4/CD49d Reference Antibody (natalizumab)Anti-Integrin a4/ITGA4/CD49d Reference Antibody (natalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-2-sec-hplc.jpgAnti-Integrin a4/ITGA4/CD49d Reference Antibody (natalizumab)The purity of Anti-Integrin a4/ITGA4/CD49d Reference Antibody (natalizumab)is more than 98.72% https://www.bosterbio.com/catalog/product/view/id/1275782026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-6-sds-page.jpgAnti-PDCD1/PD-1/CD279 Reference Antibody (pembrolizumab)Anti-PDCD1/PD-1/CD279 Reference Antibody (pembrolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-6-sec-hplc.jpgAnti-PDCD1/PD-1/CD279 Reference Antibody (pembrolizumab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (pembrolizumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-6-od450.jpgAnti-PDCD1/PD-1/CD279 Reference Antibody (pembrolizumab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (pembrolizumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-6-syngenic-mc38-cell-model.jpgAnti-PDCD1/PD-1/CD279 Reference Antibody (pembrolizumab)Pembrolizumab inhibited the tumor growth of MC38 on human PD-1 mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1275792026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-6-sds-page.jpgAnti-CD20 Reference Antibody (rituximab)Anti-CD20 Reference Antibody (rituximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-6-sec-hplc.jpgAnti-CD20 Reference Antibody (rituximab)The purity of Anti-CD20 Reference Antibody (rituximab)is more than 98.97%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-6-od450.jpgAnti-CD20 Reference Antibody (rituximab)Immobilized human EGFR His at 2 &mug/mL can bind Anti-CD20 Reference Antibody (rituximab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-6-facs.jpgAnti-CD20 Reference Antibody (rituximab)Raji cells were stained with Anti-CD20 Reference Antibody (rituximab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-6-lysis.jpgAnti-CD20 Reference Antibody (rituximab)Anti-CD20 Reference Antibody (rituximab)-induced CDC activity was evaluated using Raji Cell. The max Lysis rate was approximately 74%.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-6-lysis-1.jpgAnti-CD20 Reference Antibody (rituximab)Anti-CD20 Reference Antibody (rituximab)-induced ADCC activity was evaluated using Raji Cell. The max Lysis rate was approximately 35%. https://www.bosterbio.com/catalog/product/view/id/1275802026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-5-sds-page.jpgAnti-CD3e Reference Antibody (teplizumab)Anti-CD3e Reference Antibody (teplizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-5-sec-hplc.jpgAnti-CD3e Reference Antibody (teplizumab)The purity of Anti-CD3e Reference Antibody (teplizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1275812026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-2-sds-page.jpgAnti-IL-6Ra/CD126 Reference Antibody (tocilizumab)Anti-IL-6Ra/CD126 Reference Antibody (tocilizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-2-sec-hplc.jpgAnti-IL-6Ra/CD126 Reference Antibody (tocilizumab)The purity of Anti-IL-6Ra/CD126 Reference Antibody (tocilizumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-2-facs.jpgAnti-IL-6Ra/CD126 Reference Antibody (tocilizumab)Human IL-6R CHOs cells were stained with Anti-IL-6Ra/CD126 Reference Antibody (tocilizumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-2-facs-1.jpgAnti-IL-6Ra/CD126 Reference Antibody (tocilizumab)Anti-IL-6Ra/CD126 Reference Antibody (tocilizumab)-induced FACS Blocking activity was evaluated using Human IL-6R CHO cells. The IC50 was approximately 1.303nM. https://www.bosterbio.com/catalog/product/view/id/1275822026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-5-sds-page.jpgAnti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab)Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-5-sec-hplc.jpgAnti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-5-od450.jpgAnti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab)Immobilized human HER2https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-5-facs.jpgAnti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab)BT474 cells were stained with Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-5-xenograft-bt474-cell-model.jpgAnti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab)Trastuzumab inhibited the tumor growth of BT474 on NCG mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1275832026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-3-sds-page.jpgAnti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (vedolizumab)Anti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (vedolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-3-sec-hplc.jpgAnti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (vedolizumab)The purity of Anti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (vedolizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1275842026-03-10T04:38:22+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1275852026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1304.pngHuman SIGLEC-1/CD169 PicoKine® Quick ELISA KitHuman Cathepsin V PicoKine ELISA Kitstandard curve https://www.bosterbio.com/catalog/product/view/id/1275862026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek2039.pngHuman ANGPTL2 PicoKine® Quick ELISA KitHuman CCL25/TECK PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275872026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0392.pngHuman IL-1β PicoKine® Quick ELISA KitHuman CD169/SIGLEC-1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275882026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1484.pngHuman ADAM15 PicoKine® Quick ELISA KitMouse MCP-1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275892026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0397.pngHuman IL-2 PicoKine® Quick ELISA KitHuman ADAM15 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275902026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1357.pngHuman Biglycan PicoKine® Quick ELISA KitHuman CCL16/HCC-4 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275912026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1425.pngHuman caspase3 PicoKine® Quick ELISA KitRat TNF alpha PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275922026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0441.pngHuman MCP-1 PicoKine® Quick ELISA KitHuman IL-2 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275932026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1287.jpgMouse CD6 PicoKine® Quick ELISA KitMouse CD6 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275942026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1402.pngHuman CD97 PicoKine® Quick ELISA KitHuman R-Spondin-1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275952026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1929.pngHuman Cathepsin V PicoKine® Quick ELISA KitHuman ANGPTL7 PicoKine ELISA Kit Standard Curve https://www.bosterbio.com/catalog/product/view/id/1275962026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1127.pngHuman CCL16/HCC-4 PicoKine® Quick ELISA KitHuman MCP-1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275972026-03-10T04:38:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1516.pngHuman R-Spondin1 PicoKine® Quick ELISA KitRat IL-1 beta PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275982026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0526.jpgRat TNFα PicoKine® Quick ELISA KitRat TNF alpha PicoKine Quick ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1275992026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0393.pngRat IL-1 Beta/IL-1F2/IL1B PicoKine® Quick ELISA KitHuman ANGPTL2 PicoKine ELISA Kit Standard Curve https://www.bosterbio.com/catalog/product/view/id/1276002026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek2035.pngHuman ANGPTL7 PicoKine® Quick ELISA KitMouse IL-1 beta PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1276012026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0394.pngMouse IL-1 Beta/IL-1F2/IL1B PicoKine® Quick ELISA KitHuman IL-1 beta PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1276022026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1145.pngHuman CCL25/TECK PicoKine® Quick ELISA KitMouse CD6 PicoKine ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-drosophila-melanogaster-fruit-fly-rhogap100f-antibody-dz41617-boster.html2026-03-10T04:38:23+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-human-cenpu-dz41627-boster.html2026-03-10T04:38:23+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-mus-musculus-papillomavirus-type-1-e6-antibody-dz41639-boster.html2026-03-10T04:38:23+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-zebrafish-gpr179-antibody.html2026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/d/z/dz41643-gpr179-primary-antibodies-ihc-testing-1.jpgAnti-Zebrafish gpr179 Antibody IHC analysis of Gpr179 using anti-Gpr179 antibody (DZ41643). Gpr179 was detected in paraffin-embedded section of zebrafish brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Gpr179 Antibody (DZ41643) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/d/z/dz41643-gpr179-primary-antibodies-ihc-testing-2.jpgAnti-Zebrafish gpr179 Antibody IHC analysis of Gpr179 using anti-Gpr179 antibody (DZ41643). Gpr179 was detected in paraffin-embedded section of zebrafish brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Gpr179 Antibody (DZ41643) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/anti-mouse-atxn7-antibody-dz41648-boster.html2026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/d/z/dz41648-julien_philippe-wb.pngAnti-Mouse Atxn7 AntibodyWestern blot analysis of Atxn7 using anti-Atxn7 antibody (DZ41648). Electrophoresis was performed on a 4–20% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 µg of protein sample mixed with 4× Laemmli Sample Buffer and 2-mercaptoethanol and heated at 95 °C for 5 min prior to loading. Lane 1: mouse 3T3 cell (WT), Lane 2: mouse 3T3 cell (WT + Dox), Lane 3: mouse 3T3 cell (Scramble shRNA), Lane 4: mouse 3T3 cell (Scramble shRNA + Dox), Lane 5: mouse 3T3 cell (Atxn7 shRNA), Lane 6: mouse 3T3 cell (Atxn7 shRNA + Dox), Lane 7: mouse 3T3 cell (WT), Lane 8: mouse 3T3 cell (WT + Dox), Lane 9: mouse 3T3 cell (Scramble shRNA), Lane 10: mouse 3T3 cell (Scramble shRNA + Dox), Lane 11: mouse 3T3 cell (Atxn7 shRNA), Lane 12: mouse 3T3 cell (Atxn7 shRNA + Dox). After electrophoresis, proteins were transferred to 0.45 μm PVDF membrane at 150 mA for 50-90 minutes. Blocked the membrane in 5% non-fat dry milk in TBST (1X TBS with 0.05% Tween-20) for 30 min at RT. The membrane was incubated with rabbit anti-Atxn7 antigen affinity purified polyclonal antibody (DZ41648) at 1:1000 overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:4000 for 1 hour at RT. The signal is developed using SuperSignal West Pico PLUS and imaged on a ChemiDoc MP system. A specific band was detected for Atxn7 at approximately 100-130 kDa. https://www.bosterbio.com/catalog/product/view/id/1276132026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41273-3-4-1bbl-sds-page.pngHuman recombinant 4-1BBL (4-1BB ligand) protein, AFSDS- PAGE analysis of recombinant human 4-1BBL https://www.bosterbio.com/catalog/product/view/id/1276142026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09529-3-activin-b-sds-page.pngHuman recombinant Activin B protein, AFSDS- PAGE analysis of recombinant human Activin B https://www.bosterbio.com/catalog/product/view/id/1276152026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9ung2-7-aitrl-sds-page.pngHuman recombinant AITRL (Activation-induced TNFR member ligand) protein, AFSDS- PAGE analysis of recombinant human AITRL https://www.bosterbio.com/catalog/product/view/id/1276162026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08758-2-annexin-v-sds-page.pngHuman recombinant Annexin V protein, AFSDS- PAGE analysis of recombinant human Annexin V https://www.bosterbio.com/catalog/product/view/id/1276172026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protaaq91388-april-sds-page.pngHuman recombinant APRIL (A proliferation-inducing ligand) protein, AFSDS- PAGE analysis of recombinant human APRIL https://www.bosterbio.com/catalog/product/view/id/1276182026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9y275-6-baff-sds-page.pngHuman recombinant BAFF (B-cell activating factor) protein, AFSDS- PAGE analysis of recombinant human BAFF https://www.bosterbio.com/catalog/product/view/id/1276192026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01138-5-beta-ngf-sds-page.pngHuman recombinant beta-NGF (Nerve growth factor-beta) protein, AFSDS- PAGE analysis of recombinant human beta-NGF https://www.bosterbio.com/catalog/product/view/id/1276202026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95393-2-bmp-10-sds-page.pngHuman recombinant BMP-10 (Bone morphogenetic protein-10) protein, AFSDS- PAGE analysis of recombinant human BMP-10 https://www.bosterbio.com/catalog/product/view/id/1276212026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95390-4-bmp-11-sds-page.pngHuman recombinant BMP-11 (Bone morphogenetic protein-11) protein, AFSDS- PAGE analysis of recombinant human BMP-11 https://www.bosterbio.com/catalog/product/view/id/1276222026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq7z4p5-2-bmp-12-sds-page.pngHuman recombinant BMP-12 (Bone morphogenetic protein-12) protein, AFSDS- PAGE analysis of recombinant human BMP-12 https://www.bosterbio.com/catalog/product/view/id/1276232026-03-10T04:38:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6kf10-2-bmp-13-sds-page.pngHuman recombinant BMP-13 (Bone morphogenetic protein-13) protein, AFSDS- PAGE analysis of recombinant human BMP-13 https://www.bosterbio.com/catalog/product/view/id/1276242026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp43026-4-bmp-14-sds-page.pngHuman recombinant BMP-14 (Bone morphogenetic protein-14) protein, AFSDS- PAGE analysis of recombinant human BMP-14 https://www.bosterbio.com/catalog/product/view/id/1276252026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95972-bmp-15-sds-page.pngHuman recombinant BMP-15 (Bone morphogenetic protein-15) protein, AFSDS- PAGE analysis of recombinant human BMP-15 https://www.bosterbio.com/catalog/product/view/id/1276262026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq96s42-bmp-16-sds-page.pngHuman recombinant BMP-16 (Bone morphogenetic protein-16) protein, AFSDS- PAGE analysis of recombinant human BMP-16 https://www.bosterbio.com/catalog/product/view/id/1276272026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12643-7-bmp-2-sds-page.pngHuman recombinant BMP-2 (Bone morphogenetic protein-2) protein, AFSDS- PAGE analysis of recombinant human BMP-2 https://www.bosterbio.com/catalog/product/view/id/1276282026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12645-2-bmp-3-sds-page.pngHuman recombinant BMP-3 (Bone morphogenetic protein-3) protein, AFSDS- PAGE analysis of recombinant human BMP-3 https://www.bosterbio.com/catalog/product/view/id/1276292026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12644-5-bmp-4-sds-page.pngHuman recombinant BMP-4 (Bone morphogenetic protein-4) protein, AFSDS- PAGE analysis of recombinant human BMP-4 https://www.bosterbio.com/catalog/product/view/id/1276302026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp22003-3-bmp-5-sds-page.pngHuman recombinant BMP-5 (Bone morphogenetic protein-5) protein, AFSDS- PAGE analysis of recombinant human BMP-5 https://www.bosterbio.com/catalog/product/view/id/1276312026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp22004-4-bmp-6-sds-page.pngHuman recombinant BMP-6 (Bone morphogenetic protein-6) protein, AFSDS- PAGE analysis of recombinant human BMP-6 https://www.bosterbio.com/catalog/product/view/id/1276322026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp18075-7-bmp-7-sds-page.pngHuman recombinant BMP-7 (Bone morphogenetic protein-7) protein, AFSDS- PAGE analysis of recombinant human BMP-7 https://www.bosterbio.com/catalog/product/view/id/1276332026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq7z5y6-2-bmp-8a-sds-page.pngHuman recombinant BMP-8a (Bone morphogenetic protein-8a) protein, AFSDS- PAGE analysis of recombinant human BMP-8a https://www.bosterbio.com/catalog/product/view/id/1276342026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp34820-4-bmp-8b-sds-page.pngHuman recombinant BMP-8b (Bone morphogenetic protein-8b) protein, AFSDS- PAGE analysis of recombinant human BMP-8b https://www.bosterbio.com/catalog/product/view/id/1276352026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9uk05-1-bmp-9-sds-page.pngHuman recombinant BMP-9 (Bone morphogenetic protein-9) protein, AFSDS- PAGE analysis of recombinant human BMP-9 https://www.bosterbio.com/catalog/product/view/id/1276362026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13500-5-ccl2-sds-page.pngHuman recombinant CCL2 (C-C motif chemokine ligand 2) protein, AFSDS- PAGE analysis of recombinant human CCL2 https://www.bosterbio.com/catalog/product/view/id/1276372026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10147-4-ccl3-sds-page.pngHuman recombinant CCL3 (C-C motif chemokine ligand 3) protein, AFSDS- PAGE analysis of recombinant human CCL3 https://www.bosterbio.com/catalog/product/view/id/1276382026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13236-2-ccl4-sds-page.pngHuman recombinant CCL4 (C-C motif chemokine ligand 4) protein, AFSDS- PAGE analysis of recombinant human CCL4 https://www.bosterbio.com/catalog/product/view/id/1276392026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp32970-5-cd27l-sds-page.pngHuman recombinant CD27L (CD27 ligand) protein, AFSDS- PAGE analysis of recombinant human CD27L https://www.bosterbio.com/catalog/product/view/id/1276402026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10747-2-cd28-ecd-sds-page.pngHuman recombinant CD28 ECD protein, AFSDS- PAGE analysis of recombinant human CD28 ECD https://www.bosterbio.com/catalog/product/view/id/1276412026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp32971-5-cd30l-sds-page.pngHuman recombinant CD30L (CD30 ligand) protein, AFSDS- PAGE analysis of recombinant human CD30L https://www.bosterbio.com/catalog/product/view/id/1276422026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16422-4-cd326-sds-page.pngHuman recombinant CD326 protein, AFSDS- PAGE analysis of recombinant human CD326 https://www.bosterbio.com/catalog/product/view/id/1276432026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp29965-5-cd40l-sds-page.pngHuman recombinant CD40L (CD40 ligand) protein, AFSDS- PAGE analysis of recombinant human CD40L https://www.bosterbio.com/catalog/product/view/id/1276442026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq49ah0-2-cdnf-sds-page.pngHuman recombinant CDNF (Cerebral dopamine neurotrophic factor) protein, AFSDS- PAGE analysis of recombinant human CDNF https://www.bosterbio.com/catalog/product/view/id/1276452026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp36222-4-chi3l1-sds-page.pngHuman recombinant CHI3L1 (Chitinase-3-like protein 1) protein, AFSDS- PAGE analysis of recombinant human CHI3L1 https://www.bosterbio.com/catalog/product/view/id/1276462026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26441-8-cntf-sds-page.pngHuman recombinant CNTF (Ciliary neurotrophic factor) protein, AFSDS- PAGE analysis of recombinant human CNTF https://www.bosterbio.com/catalog/product/view/id/1276472026-03-10T04:38:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09341-4-cxcl1-sds-page.pngHuman recombinant CXCL1 (C-X-C motif chemokine 1) protein, AFSDS- PAGE analysis of recombinant human CXCL1 https://www.bosterbio.com/catalog/product/view/id/1276482026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp02778-3-cxcl10-sds-page.pngHuman recombinant CXCL10 (C-X-C motif chemokine 10) protein, AFSDS- PAGE analysis of recombinant human CXCL10 https://www.bosterbio.com/catalog/product/view/id/1276492026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto14625-4-cxcl11-sds-page.pngHuman recombinant CXCL11 (C-X-C motif chemokine 11) protein, AFSDS- PAGE analysis of recombinant human CXCL11 https://www.bosterbio.com/catalog/product/view/id/1276502026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp48061-8-cxcl12-sds-page.pngHuman recombinant CXCL12 (24-88) (C-X-C motif chemokine 12) protein, AFSDS- PAGE analysis of recombinant human CXCL12 https://www.bosterbio.com/catalog/product/view/id/1276512026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto43927-4-cxcl13-sds-page.pngHuman recombinant CXCL13 (C-X-C motif chemokine 13) protein, AFSDS- PAGE analysis of recombinant human CXCL13 https://www.bosterbio.com/catalog/product/view/id/1276522026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp19875-4-cxcl2-sds-page.pngHuman recombinant CXCL2 (C-X-C motif chemokine 2) protein, AFSDS- PAGE analysis of recombinant human CXCL2 https://www.bosterbio.com/catalog/product/view/id/1276532026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp19876-4-cxcl3-sds-page.pngHuman recombinant CXCL3 (C-X-C motif chemokine 3) protein, AFSDS- PAGE analysis of recombinant human CXCL3 https://www.bosterbio.com/catalog/product/view/id/1276542026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp02776-6-cxcl4-sds-page.pngHuman recombinant CXCL4 (C-X-C motif chemokine 4) protein, AFSDS- PAGE analysis of recombinant human CXCL4 https://www.bosterbio.com/catalog/product/view/id/1276552026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp42830-4-cxcl5-sds-page.pngHuman recombinant CXCL5 (C-X-C motif chemokine 5) protein, AFSDS- PAGE analysis of recombinant human CXCL5 https://www.bosterbio.com/catalog/product/view/id/1276562026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp80162-2-cxcl6-sds-page.pngHuman recombinant CXCL6 (C-X-C motif chemokine 6) protein, AFSDS- PAGE analysis of recombinant human CXCL6 https://www.bosterbio.com/catalog/product/view/id/1276572026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp02775-3-cxcl7-sds-page.pngHuman recombinant CXCL7 (C-X-C motif chemokine 7) protein, AFSDS- PAGE analysis of recombinant human CXCL7 https://www.bosterbio.com/catalog/product/view/id/1276582026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq07325-4-cxcl9-sds-page.pngHuman recombinant CXCL9 (C-X-C motif chemokine 9) protein, AFSDS- PAGE analysis of recombinant human CXCL9 https://www.bosterbio.com/catalog/product/view/id/1276592026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01133-5-egf-sds-page.pngHuman recombinant EGF (Epidermal growth factor) protein, AFSDS- PAGE analysis of recombinant human EGF https://www.bosterbio.com/catalog/product/view/id/1276602026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp06733-2-eno1-sds-page.pngHuman recombinant ENO1 protein, AFSDS- PAGE analysis of recombinant human ENO1 https://www.bosterbio.com/catalog/product/view/id/1276612026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp48023-4-fasl-sds-page.pngHuman recombinant FasL (Fas ligand) protein, AFSDS- PAGE analysis of recombinant human FasL https://www.bosterbio.com/catalog/product/view/id/1276622026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05230-4-fgf-1-sds-page.pngHuman recombinant FGF-1 (Fibroblast growth factor-acidic) protein, AFSDS- PAGE analysis of recombinant human FGF-1 https://www.bosterbio.com/catalog/product/view/id/1276632026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto15520-4-fgf-10-sds-page.pngHuman recombinant FGF-10 (Fibroblast growth factor-10) protein, AFSDS- PAGE analysis of recombinant human FGF-10 https://www.bosterbio.com/catalog/product/view/id/1276642026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq92914-fgf-11-isoform-1-sds-page.pngHuman recombinant FGF-11 isoform 1 (Fibroblast growth factor-11 isoform 1) protein, AFSDS- PAGE analysis of recombinant human FGF-11 isoform 1 https://www.bosterbio.com/catalog/product/view/id/1276652026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq92914-1-fgf-11-isoform-2-sds-page.pngHuman recombinant FGF-11 isoform 2 (Fibroblast growth factor-11 isoform 2) protein, AFSDS- PAGE analysis of recombinant human FGF-11 isoform 2 https://www.bosterbio.com/catalog/product/view/id/1276662026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp61328-2-fgf-12-sds-page.pngHuman recombinant FGF-12 (Fibroblast growth factor-12) protein, AFSDS- PAGE analysis of recombinant human FGF-12 https://www.bosterbio.com/catalog/product/view/id/1276672026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq92913-1-fgf-13-sds-page.pngHuman recombinant FGF-13 (Fibroblast growth factor-13) protein, AFSDS- PAGE analysis of recombinant human FGF-13 https://www.bosterbio.com/catalog/product/view/id/1276682026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq92915-2-fgf-14-sds-page.pngHuman recombinant FGF-14 (Fibroblast growth factor-14) protein, AFSDS- PAGE analysis of recombinant human FGF-14 https://www.bosterbio.com/catalog/product/view/id/1276692026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto43320-2-fgf-16-sds-page.pngHuman recombinant FGF-16 (Fibroblast growth factor-16) protein, AFSDS- PAGE analysis of recombinant human FGF-16 https://www.bosterbio.com/catalog/product/view/id/1276702026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto60258-4-fgf-17-sds-page.pngHuman recombinant FGF-17 (Fibroblast growth factor-17) protein, AFSDS- PAGE analysis of recombinant human FGF-17 https://www.bosterbio.com/catalog/product/view/id/1276712026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto76093-3-fgf-18-sds-page.pngHuman recombinant FGF-18 (Fibroblast growth factor-18) protein, AFSDS- PAGE analysis of recombinant human FGF-18 https://www.bosterbio.com/catalog/product/view/id/1276722026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95750-4-fgf-19-sds-page.pngHuman recombinant FGF-19 (Fibroblast growth factor-19) protein, AFSDS- PAGE analysis of recombinant human FGF-19 https://www.bosterbio.com/catalog/product/view/id/1276742026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9np95-2-fgf-20-sds-page.pngHuman recombinant FGF-20 (Fibroblast growth factor-20) protein, AFSDS- PAGE analysis of recombinant human FGF-20 https://www.bosterbio.com/catalog/product/view/id/1276752026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nsa1-4-fgf-21-sds-page.pngHuman recombinant FGF-21 (Fibroblast growth factor-21) protein, AFSDS- PAGE analysis of recombinant human FGF-21 https://www.bosterbio.com/catalog/product/view/id/1276762026-03-10T04:38:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9hct0-1-fgf-22-sds-page.pngHuman recombinant FGF-22 (Fibroblast growth factor-22) protein, AFSDS- PAGE analysis of recombinant human FGF-22 https://www.bosterbio.com/catalog/product/view/id/1276772026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9gzv9-5-fgf-23-sds-page.pngHuman recombinant FGF-23 (Fibroblast growth factor-23) protein, AFSDS- PAGE analysis of recombinant human FGF-23 https://www.bosterbio.com/catalog/product/view/id/1276782026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp11487-fgf-3-sds-page.pngHuman recombinant FGF-3 (Fibroblast growth factor-3) protein, AFSDS- PAGE analysis of recombinant human FGF-3 https://www.bosterbio.com/catalog/product/view/id/1276792026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08620-3-fgf-4-sds-page.pngHuman recombinant FGF-4 (Fibroblast growth factor-4) protein, AFSDS- PAGE analysis of recombinant human FGF-4 https://www.bosterbio.com/catalog/product/view/id/1276802026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12034-2-fgf-5-sds-page.pngHuman recombinant FGF-5 (Fibroblast growth factor-5) protein, AFSDS- PAGE analysis of recombinant human FGF-5 https://www.bosterbio.com/catalog/product/view/id/1276812026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10767-2-fgf-6-sds-page.pngHuman recombinant FGF-6 (Fibroblast growth factor-6) protein, AFSDS- PAGE analysis of recombinant human FGF-6 https://www.bosterbio.com/catalog/product/view/id/1276822026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp55075-4-fgf-8a-sds-page.pngHuman recombinant FGF-8a (Fibroblast growth factor-8a) protein, AFSDS- PAGE analysis of recombinant human FGF-8a https://www.bosterbio.com/catalog/product/view/id/1276832026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp55075-5-fgf-8b-sds-page.pngHuman recombinant FGF-8b (Fibroblast growth factor-8b) protein, AFSDS- PAGE analysis of recombinant human FGF-8b https://www.bosterbio.com/catalog/product/view/id/1276842026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp31371-2-fgf-9-sds-page.pngHuman recombinant FGF-9 (Fibroblast growth factor-9) protein, AFSDS- PAGE analysis of recombinant human FGF-9 https://www.bosterbio.com/catalog/product/view/id/1276852026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49771-7-flt-3-ligand-sds-page.pngHuman recombinant Flt-3 Ligand (Fms-related tyrosine kinase-3 ligand) protein, AFSDS- PAGE analysis of recombinant human Flt-3 Ligand https://www.bosterbio.com/catalog/product/view/id/1276862026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09382-3-galectin-1-sds-page.pngHuman recombinant Galectin-1 protein, AFSDS- PAGE analysis of recombinant human Galectin-1 https://www.bosterbio.com/catalog/product/view/id/1276872026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq05315-2-galectin-10-sds-page.pngHuman recombinant Galectin-10 protein, AFSDS- PAGE analysis of recombinant human Galectin-10 https://www.bosterbio.com/catalog/product/view/id/1276882026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq96dt0-2-galectin-12-sds-page.pngHuman recombinant Galectin-12 protein, AFSDS- PAGE analysis of recombinant human Galectin-12 https://www.bosterbio.com/catalog/product/view/id/1276892026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9uhv8-2-galectin-13-sds-page.pngHuman recombinant Galectin-13 protein, AFSDS- PAGE analysis of recombinant human Galectin-13 https://www.bosterbio.com/catalog/product/view/id/1276902026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8tce9-2-galectin-14-sds-page.pngHuman recombinant Galectin-14 protein, AFSDS- PAGE analysis of recombinant human Galectin-14 https://www.bosterbio.com/catalog/product/view/id/1276912026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota8mum7-1-galectin-16-sds-page.pngHuman recombinant Galectin-16 protein, AFSDS- PAGE analysis of recombinant human Galectin-16 https://www.bosterbio.com/catalog/product/view/id/1276922026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05162-2-galectin-2-sds-page.pngHuman recombinant Galectin-2 protein, AFSDS- PAGE analysis of recombinant human Galectin-2 https://www.bosterbio.com/catalog/product/view/id/1276932026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp17931-4-galectin-3-sds-page.pngHuman recombinant Galectin-3 protein, AFSDS- PAGE analysis of recombinant human Galectin-3 https://www.bosterbio.com/catalog/product/view/id/1276942026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp56470-2-galectin-4-sds-page.pngHuman recombinant Galectin-4 protein, AFSDS- PAGE analysis of recombinant human Galectin-4 https://www.bosterbio.com/catalog/product/view/id/1276952026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp47929-3-galectin-7-sds-page.pngHuman recombinant Galectin-7 protein, AFSDS- PAGE analysis of recombinant human Galectin-7 https://www.bosterbio.com/catalog/product/view/id/1276962026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto00214-3-galectin-8-sds-page.pngHuman recombinant Galectin-8 protein, AFSDS- PAGE analysis of recombinant human Galectin-8 https://www.bosterbio.com/catalog/product/view/id/1276972026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto00182-2-galectin-9-sds-page.pngHuman recombinant Galectin-9 protein, AFSDS- PAGE analysis of recombinant human Galectin-9 https://www.bosterbio.com/catalog/product/view/id/1276982026-03-10T04:38:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq99062-3-g-csf-sds-page.pngHuman recombinant G-CSF (Granulocyte colony-stimulating factor) protein, AFSDS- PAGE analysis of recombinant human G-CSF https://www.bosterbio.com/catalog/product/view/id/1276992026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp39905-3-gdnf-sds-page.pngHuman recombinant GDNF (Glial-derived neurotrophic factor) protein, AFSDS- PAGE analysis of recombinant human GDNF https://www.bosterbio.com/catalog/product/view/id/1277002026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14136-gfap-sds-page.pngHuman recombinant GFAP protein, AFSDS- PAGE analysis of recombinant human GFAP https://www.bosterbio.com/catalog/product/view/id/1277012026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp27352-1-gif-sds-page.pngHuman recombinant GIF (Gastric intrinsic factor) protein, AFSDS- PAGE analysis of recombinant human GIF https://www.bosterbio.com/catalog/product/view/id/1277022026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp17900-2-gm2a-sds-page.pngHuman recombinant GM2A protein, AFSDS- PAGE analysis of recombinant human GM2A https://www.bosterbio.com/catalog/product/view/id/1277032026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp04141-8-gm-csf-sds-page.pngHuman recombinant GM-CSF (Granulocyte-macrophage colony-stimulating factor) protein, AFSDS- PAGE analysis of recombinant human GM-CSF https://www.bosterbio.com/catalog/product/view/id/1277042026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp51858-2-hdgf-sds-page.pngHuman recombinant HDGF (Hepatoma-derived growth factor) protein, AFSDS- PAGE analysis of recombinant human HDGF https://www.bosterbio.com/catalog/product/view/id/1277052026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq02297-3-heregulin-beta-1-sds-page.pngHuman recombinant Heregulin Beta 1 protein, AFSDS- PAGE analysis of recombinant human Heregulin https://www.bosterbio.com/catalog/product/view/id/1277062026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14210-8-hgf-sds-page.pngHuman recombinant HGF protein, AFSDS- PAGE analysis of recombinant human HGF https://www.bosterbio.com/catalog/product/view/id/1277072026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09429-3-hmgb1-sds-page.pngHuman recombinant HMGB1 (High mobility group box 1) protein, AFSDS- PAGE analysis of recombinant human HMGB1 https://www.bosterbio.com/catalog/product/view/id/1277082026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09429-4-hmgb1-c23ac45a-sds-page.pngHuman (mammalian cell expression) recombinant HMGB1 C23AC45A protein, AFSDS- PAGE analysis of recombinant human HMGB1 C23AC45A https://www.bosterbio.com/catalog/product/view/id/1277092026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09429-5-hmgb1-c23ac45ac106a-sds-page.pngHuman (mammalian cell expression) recombinant HMGB1 C23AC45AC106A protein, AFSDS- PAGE analysis of recombinant human HMGB1 C23AC45AC10?A https://www.bosterbio.com/catalog/product/view/id/1277102026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09429-6-hmgb1-sds-page.pngHuman (mammalian cell expression) recombinant HMGB1 protein, AFSDS- PAGE analysis of recombinant human HMGB1 https://www.bosterbio.com/catalog/product/view/id/1277112026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26583-2-hmgb2-sds-page.pngHuman recombinant HMGB2 (High mobility group box 2) protein, AFSDS- PAGE analysis of recombinant human HMGB2 https://www.bosterbio.com/catalog/product/view/id/1277122026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26583-3-hmgb2-sds-page.pngHuman (mammalian cell expression) recombinant HMGB2 protein, AFSDS- PAGE analysis of recombinant human HMGB2 https://www.bosterbio.com/catalog/product/view/id/1277132026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01562-2-ifn-alpha-1a-sds-page.pngHuman recombinant IFN alpha 1a (Interferon alpha 1a) protein, AFSDS- PAGE analysis of recombinant human IFN alpha 1a https://www.bosterbio.com/catalog/product/view/id/1277142026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01574-4-ifn-beta-1a-sds-page.pngHuman recombinant IFN beta 1a (Interferon beta 1a) protein, AFSDS- PAGE analysis of recombinant human IFN beta 1a https://www.bosterbio.com/catalog/product/view/id/1277152026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01579-9-ifn-gamma-sds-page.pngHuman recombinant IFN gamma (Interferon gamma) protein, AFSDS- PAGE analysis of recombinant human IFN gamma https://www.bosterbio.com/catalog/product/view/id/1277162026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05000-3-ifn-omega-sds-page.pngHuman recombinant IFN omega (interferon omega) protein, AFSDS- PAGE analysis of recombinant human IFN omega https://www.bosterbio.com/catalog/product/view/id/1277172026-03-10T04:38:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq16270-4-igfbp7-sds-page.pngHuman recombinant IGFBP7(IGF-binding protein 7) protein, AFSDS- PAGE analysis of recombinant human IGFBP7 https://www.bosterbio.com/catalog/product/view/id/1277182026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05019-3-igf-i-sds-page.pngHuman recombinant IGF-I (Insulin-like growth factor-I) protein, AFSDS- PAGE analysis of recombinant human IGF-I https://www.bosterbio.com/catalog/product/view/id/1277192026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01344-3-igf-ii-sds-page.pngHuman recombinant IGF-II (Insulin-like growth factor-II) protein, AFSDS- PAGE analysis of recombinant human IGF-II https://www.bosterbio.com/catalog/product/view/id/1277202026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01583-7-il-1-alpha-sds-page.pngHuman recombinant IL-1 alpha (Interleukin-1 alpha) protein, AFSDS- PAGE analysis of recombinant human IL-1 alpha https://www.bosterbio.com/catalog/product/view/id/1277212026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01584-5-il-1-beta-sds-page.pngHuman recombinant IL-1 beta (Interleukin-1 beta) protein, AFSDS- PAGE analysis of recombinant human IL-1 beta https://www.bosterbio.com/catalog/product/view/id/1277222026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp22301-5-il-10-sds-page.pngHuman recombinant IL-10 (Interleukin-10) protein, AFSDS- PAGE analysis of recombinant human IL-10 https://www.bosterbio.com/catalog/product/view/id/1277232026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp20809-3-il-11-sds-page.pngHuman recombinant IL-11 (Interleukin-11) protein, AFSDS- PAGE analysis of recombinant human IL-11 https://www.bosterbio.com/catalog/product/view/id/1277242026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp29459-2-il-12-p70-sds-page.pngHuman recombinant IL-12 (p70) (Interleukin-12 p70) protein, AFSDS- PAGE analysis of recombinant human IL-12 p70 https://www.bosterbio.com/catalog/product/view/id/1277252026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp29459-3-il-12-p35-sds-page.pngHuman recombinant IL-12 p35 (Interleukin-12 p35) protein, AFSDS- PAGE analysis of recombinant human IL-12 p35 https://www.bosterbio.com/catalog/product/view/id/1277262026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp29460-6-il-12-p40-sds-page.pngHuman recombinant IL-12 p40 (Interleukin-12 p40) protein, AFSDS- PAGE analysis of recombinant human IL-12 p40 https://www.bosterbio.com/catalog/product/view/id/1277272026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp35225-5-il-13-sds-page.pngHuman recombinant IL-13 (Interleukin-13) protein, AFSDS- PAGE analysis of recombinant human IL-13 https://www.bosterbio.com/catalog/product/view/id/1277282026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp40933-5-il-15-sds-page.pngHuman recombinant IL-15 (Interleukin-15) protein, AFSDS- PAGE analysis of recombinant human IL-15 https://www.bosterbio.com/catalog/product/view/id/1277292026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq14005-7-il-16-sds-page.pngHuman recombinant IL-16 (aa 2-130) (Interleukin-16) protein, AFSDS- PAGE analysis of recombinant human IL-16 https://www.bosterbio.com/catalog/product/view/id/1277302026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq16552-6-il-17a-sds-page.pngHuman recombinant IL-17A (Interleukin-17A) protein, AFSDS- PAGE analysis of recombinant human IL-17A https://www.bosterbio.com/catalog/product/view/id/1277312026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9uhf5-6-il-17b-sds-page.pngHuman recombinant IL-17B (Interleukin-17B) protein, AFSDS- PAGE analysis of recombinant human IL-17B https://www.bosterbio.com/catalog/product/view/id/1277322026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8tad2-2-il-17d-sds-page.pngHuman recombinant IL-17D (Interleukin-17D) protein, AFSDS- PAGE analysis of recombinant human IL-17D https://www.bosterbio.com/catalog/product/view/id/1277332026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq96pd4-7-il-17f-sds-page.pngHuman recombinant IL-17F (Interleukin-17F) protein, AFSDS- PAGE analysis of recombinant human IL-17F https://www.bosterbio.com/catalog/product/view/id/1277342026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq14116-2-il-18-sds-page.pngHuman recombinant IL-18 (Interleukin-18) protein, AFSDS- PAGE analysis of recombinant human IL-18 https://www.bosterbio.com/catalog/product/view/id/1277352026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9uhd0-3-il-19-sds-page.pngHuman recombinant IL-19 (Interleukin-19) protein, AFSDS- PAGE analysis of recombinant human IL-19 https://www.bosterbio.com/catalog/product/view/id/1277362026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp18510-5-il-1ra-sds-page.pngHuman recombinant IL-1RA (Interleukin-1 receptor antagonist) protein, AFSDS- PAGE analysis of recombinant human IL-1RA https://www.bosterbio.com/catalog/product/view/id/1277372026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp60568-6-il-2-sds-page.pngHuman recombinant IL-2 (Interleukin-2) protein, AFSDS- PAGE analysis of recombinant human IL-2 https://www.bosterbio.com/catalog/product/view/id/1277382026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nyy1-2-il-20-sds-page.pngHuman recombinant IL-20 (Interleukin-20) protein, AFSDS- PAGE analysis of recombinant human IL-20 https://www.bosterbio.com/catalog/product/view/id/1277392026-03-10T04:38:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9hbe4-5-il-21-sds-page.pngHuman recombinant IL-21 (Interleukin-21) protein, AFSDS- PAGE analysis of recombinant human IL-21 https://www.bosterbio.com/catalog/product/view/id/1277402026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9gzx6-3-il-22-sds-page.pngHuman recombinant IL-22 (Interleukin-22) protein, AFSDS- PAGE analysis of recombinant human IL-22 https://www.bosterbio.com/catalog/product/view/id/1277412026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9npf7-3-il-23-p19-sds-page.pngHuman recombinant IL-23 p19 (Interleukin-23 p19) protein, AFSDS- PAGE analysis of recombinant human IL-23 p19 https://www.bosterbio.com/catalog/product/view/id/1277422026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq13007-2-il-24-sds-page.pngHuman recombinant IL-24 (Interleukin-24) protein, AFSDS- PAGE analysis of recombinant human IL-24 https://www.bosterbio.com/catalog/product/view/id/1277432026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9h293-3-il-25-sds-page.pngHuman recombinant IL-25 (Interleukin-25) protein, AFSDS- PAGE analysis of recombinant human IL-25 https://www.bosterbio.com/catalog/product/view/id/1277442026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nph9-3-il-26-sds-page.pngHuman recombinant IL-26 (Interleukin-26) protein, AFSDS- PAGE analysis of recombinant human IL-26 https://www.bosterbio.com/catalog/product/view/id/1277452026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq14213-3-il-27-ebi3-sds-page.pngHuman recombinant IL-27 EBI3 (Interleukin-27 EBI3) protein, AFSDS- PAGE analysis of recombinant human IL-27 EBI3 https://www.bosterbio.com/catalog/product/view/id/1277462026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8izj0-5-il-28a-sds-page.pngHuman recombinant IL-28A (Interleukin-28A) protein, AFSDS- PAGE analysis of recombinant human IL-28A https://www.bosterbio.com/catalog/product/view/id/1277472026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8izi9-3-il-28b-sds-page.pngHuman recombinant IL-28B (Interleukin-28B) protein, AFSDS- PAGE analysis of recombinant human IL-28B https://www.bosterbio.com/catalog/product/view/id/1277482026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8iu54-7-il-29-sds-page.pngHuman recombinant IL-29 (Interleukin-29) protein, AFSDS- PAGE analysis of recombinant human IL-29 https://www.bosterbio.com/catalog/product/view/id/1277492026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08700-7-il-3-sds-page.pngHuman recombinant IL-3 (Interleukin-3) protein, AFSDS- PAGE analysis of recombinant human IL-3 https://www.bosterbio.com/catalog/product/view/id/1277502026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8nev9-1-il-30-sds-page.pngHuman recombinant IL-30 (Interleukin-30) protein, AFSDS- PAGE analysis of recombinant human IL-30 https://www.bosterbio.com/catalog/product/view/id/1277512026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6ebc2-2-il-31-sds-page.pngHuman recombinant IL-31 (Interleukin-31) protein, AFSDS- PAGE analysis of recombinant human IL-31 https://www.bosterbio.com/catalog/product/view/id/1277522026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp24001-3-il-32-alpha-sds-page.pngHuman recombinant IL-32 alpha (Interleukin-32 alpha) protein, AFSDS- PAGE analysis of recombinant human IL-32 alpha https://www.bosterbio.com/catalog/product/view/id/1277532026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95760-4-il-33-sds-page.pngHuman recombinant IL-33 (Interleukin-33) protein, AFSDS- PAGE analysis of recombinant human IL-33 https://www.bosterbio.com/catalog/product/view/id/1277542026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6zmj4-5-il-34-sds-page.pngHuman recombinant IL-34 (Interleukin-34) protein, AFSDS- PAGE analysis of recombinant human IL-34 https://www.bosterbio.com/catalog/product/view/id/1277552026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9uha7-2-il-36-alpha-sds-page.pngHuman recombinant IL-36 alpha (Interleukin-36 alpha) protein, AFSDS- PAGE analysis of recombinant human IL-36 alpha https://www.bosterbio.com/catalog/product/view/id/1277562026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nzh7-3-il-36-beta-sds-page.pngHuman recombinant IL-36 beta (Interleukin-36 beta) protein, AFSDS- PAGE analysis of recombinant human IL-36 beta https://www.bosterbio.com/catalog/product/view/id/1277572026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nzh8-5-il-36-gamma-sds-page.pngHuman recombinant IL-36 gamma (Interleukin-36 gamma) protein, AFSDS- PAGE analysis of recombinant human IL-36 gamma https://www.bosterbio.com/catalog/product/view/id/1277582026-03-10T04:38:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9ubh0-3-il-36ra-sds-page.pngHuman recombinant IL-36RA (Interleukin-36 receptor antagonist) protein, AFSDS- PAGE analysis of recombinant human IL-36RA https://www.bosterbio.com/catalog/product/view/id/1277592026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nzh6-1-il-37-sds-page.pngHuman recombinant IL-37 (Interleukin-37) protein, AFSDS- PAGE analysis of recombinant human IL-37 https://www.bosterbio.com/catalog/product/view/id/1277602026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8wwz1-4-il-38-sds-page.pngHuman recombinant IL-38 (Interleukin-38) protein, AFSDS- PAGE analysis of recombinant human IL-38 https://www.bosterbio.com/catalog/product/view/id/1277612026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05112-9-il-4-sds-page.pngHuman recombinant IL-4 (Interleukin-4) protein, AFSDS- PAGE analysis of recombinant human IL-4 https://www.bosterbio.com/catalog/product/view/id/1277622026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05113-4-il-5-sds-page.pngHuman recombinant IL-5 (Interleukin-5) protein, AFSDS- PAGE analysis of recombinant human IL-5 https://www.bosterbio.com/catalog/product/view/id/1277632026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05231-8-il-6-sds-page.pngHuman recombinant IL-6 (Interleukin-6) protein, AFSDS- PAGE analysis of recombinant human IL-6 https://www.bosterbio.com/catalog/product/view/id/1277642026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13232-9-il-7-sds-page.pngHuman recombinant IL-7 (Interleukin-7) protein, AFSDS- PAGE analysis of recombinant human IL-7 https://www.bosterbio.com/catalog/product/view/id/1277652026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10145-7-il-8-sds-page.pngHuman recombinant IL-8 (aa28-99) (Interleukin-8) protein, AFSDS- PAGE analysis of recombinant human IL-8 https://www.bosterbio.com/catalog/product/view/id/1277662026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15248-6-il-9-sds-page.pngHuman recombinant IL-9 (Interleukin-9) protein, AFSDS- PAGE analysis of recombinant human IL-9 https://www.bosterbio.com/catalog/product/view/id/1277672026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15018-8-lif-sds-page.pngHuman recombinant LIF protein, AFSDS- PAGE analysis of recombinant human LIF https://www.bosterbio.com/catalog/product/view/id/1277682026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto43557-3-light-sds-page.pngHuman recombinant LIGHT protein, AFSDS- PAGE analysis of recombinant human LIGHT https://www.bosterbio.com/catalog/product/view/id/1277692026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09603-8-m-csf-sds-page.pngHuman recombinant M-CSF (Macrophage colony stimulating factor) protein, AFSDS- PAGE analysis of recombinant human M-CSF https://www.bosterbio.com/catalog/product/view/id/1277702026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp21741-3-midkine-sds-page.pngHuman recombinant Midkine protein, AFSDS- PAGE analysis of recombinant human Midkine https://www.bosterbio.com/catalog/product/view/id/1277712026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14174-9-mif-sds-page.pngHuman recombinant MIF (Macrophage migration inhibitory factor) protein, AFSDS- PAGE analysis of recombinant human MIF https://www.bosterbio.com/catalog/product/view/id/1277722026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08253-4-mmp2-sds-page.pngHuman recombinant MMP2 (active) protein, AFSDS- PAGE analysis of recombinant human MMP2 (active) https://www.bosterbio.com/catalog/product/view/id/1277732026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09237-3-mmp7-sds-page.pngHuman recombinant MMP7 (active) protein, AFSDS- PAGE analysis of recombinant human MMP7 (active) https://www.bosterbio.com/catalog/product/view/id/1277742026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09237-4-mmp7-sds-page.pngHuman recombinant MMP7 (proenzyme) protein, AFSDS- PAGE analysis of recombinant human MMP7 (proenzyme) https://www.bosterbio.com/catalog/product/view/id/1277752026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq13496-mtm1-sds-page.pngHuman recombinant MTM1 protein, AFSDS- PAGE analysis of recombinant human MTM1 https://www.bosterbio.com/catalog/product/view/id/1277762026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq99748-5-neurturin-sds-page.pngHuman recombinant Neurturin protein, AFSDS- PAGE analysis of recombinant human Neurturin https://www.bosterbio.com/catalog/product/view/id/1277772026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq13253-6-noggin-sds-page.pngHuman recombinant Noggin protein, AFSDS- PAGE analysis of recombinant human Noggin https://www.bosterbio.com/catalog/product/view/id/1277782026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq02297-4-nrg1-sds-page.pngHuman recombinant NRG1 protein, AFSDS- PAGE analysis of recombinant human NRG1 https://www.bosterbio.com/catalog/product/view/id/1277792026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto15527-2-ogg1-sds-page.pngHuman recombinant OGG1 (8-oxoguanine DNA glycosylase) protein, AFSDS- PAGE analysis of recombinant human OGG1 https://www.bosterbio.com/catalog/product/view/id/1277802026-03-10T04:38:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9nzq7-3-pd-l1-sds-page.pngHuman recombinant PD-L1 protein, AFSDS- PAGE analysis of recombinant human PD-L1 https://www.bosterbio.com/catalog/product/view/id/1277812026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp0djd9-pga5-sds-page.pngHuman recombinant PGA5 (Pepsinogen A5) protein, AFSDS- PAGE analysis of recombinant human PGA5 https://www.bosterbio.com/catalog/product/view/id/1277822026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp21246-3-pleiotrophin-sds-page.pngHuman recombinant Pleiotrophin protein, AFSDS- PAGE analysis of recombinant human Pleiotrophin https://www.bosterbio.com/catalog/product/view/id/1277832026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07225-pros1-sds-page.pngHuman recombinant PROS1 protein, AFSDS- PAGE analysis of recombinant human PROS1 https://www.bosterbio.com/catalog/product/view/id/1277842026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq15109-2-rage-sds-page.pngHuman recombinant RAGE (Receptor for advanced glycation endproducts) protein, AFSDS- PAGE analysis of recombinant human RAGE https://www.bosterbio.com/catalog/product/view/id/1277852026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto14788-6-rankl-sds-page.pngHuman recombinant RANKL (Receptor activator of nuclear factor kappa-Β ligand) protein, AFSDS- PAGE analysis of recombinant human RANKL https://www.bosterbio.com/catalog/product/view/id/1277862026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq2mka7-1-r-spondin-1-sds-page.pngHuman recombinant R-spondin 1 protein, AFSDS- PAGE analysis of recombinant human R-spondin 1 https://www.bosterbio.com/catalog/product/view/id/1277872026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp21583-6-scf-sds-page.pngHuman recombinant SCF protein, AFSDS- PAGE analysis of recombinant human SCF https://www.bosterbio.com/catalog/product/view/id/1277882026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq15465-6-sonic-hedgehog-sds-page.pngHuman recombinant Sonic Hedgehog (C24II) protein, AFSDS- PAGE analysis of recombinant human Sonic Hedgehog (C24II) https://www.bosterbio.com/catalog/product/view/id/1277892026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01135-2-tgf-alpha-sds-page.pngHuman recombinant TGF alpha (Transforming growth factor alpha) protein, AFSDS- PAGE analysis of recombinant human TGF alpha https://www.bosterbio.com/catalog/product/view/id/1277912026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp61812-4-tgf-beta-2-sds-page.pngHuman recombinant TGF beta 2 (Transforming growth factor beta 2) protein, AFSDS- PAGE analysis of recombinant human TGF beta 2 https://www.bosterbio.com/catalog/product/view/id/1277922026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10600-8-tgf-beta-3-sds-page.pngHuman recombinant TGF beta 3 (Transforming growth factor beta 3) protein, AFSDS- PAGE analysis of recombinant human TGF beta 3 https://www.bosterbio.com/catalog/product/view/id/1277932026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95150-5-tl1a-sds-page.pngHuman recombinant TL1A (TNF-like ligand 1A) protein, AFSDS- PAGE analysis of recombinant human TL1A https://www.bosterbio.com/catalog/product/view/id/1277942026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01375-8-tnf-alpha-sds-page.pngHuman recombinant TNF alpha (Tumor necrosis factor alpha) protein, AFSDS- PAGE analysis of recombinant human TNF alpha https://www.bosterbio.com/catalog/product/view/id/1277952026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01374-6-tnf-beta-sds-page.pngHuman recombinant TNF beta (Tumor necrosis factor beta) protein, AFSDS- PAGE analysis of recombinant human TNF beta https://www.bosterbio.com/catalog/product/view/id/1277962026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp40225-6-tpo-sds-page.pngHuman recombinant TPO (Thrombopoietin) protein, AFSDS- PAGE analysis of recombinant human TPO https://www.bosterbio.com/catalog/product/view/id/1277972026-04-01T05:01:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp50591-6-trail-sds-page.pngHuman recombinant TRAIL (TNF-related apoptosis-inducing ligand) protein, AFSDS- PAGE analysis of recombinant human TRAIL https://www.bosterbio.com/catalog/product/view/id/1277982026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto43508-2-tweak-sds-page.pngHuman recombinant TWEAK (TNF-related weak inducer of apoptosis) protein, AFSDS- PAGE analysis of recombinant human TWEAK https://www.bosterbio.com/catalog/product/view/id/1277992026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15692-17-vegf121-sds-page.pngHuman recombinant VEGF121 (Vascular endothelial growth factor 121) protein, AFSDS- PAGE analysis of recombinant human VEGF121 https://www.bosterbio.com/catalog/product/view/id/1278002026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15692-18-vegf165-sds-page.pngHuman recombinant VEGF165 (Vascular endothelial growth factor 165) protein, AFSDS- PAGE analysis of recombinant human VEGF165 https://www.bosterbio.com/catalog/product/view/id/1278012026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08476-8-activin-a-sds-page.pngHuman/Mouse/Rat recombinant Activin A protein, AFSDS- PAGE analysis of recombinant human/mouse/rat Activin A https://www.bosterbio.com/catalog/product/view/id/1278022026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp23560-5-bdnf-sds-page.pngHuman/Mouse/Rat recombinant BDNF (Brain-derived neurotrophic factor) protein, AFSDS- PAGE analysis of recombinant human/mouse/rat BDNF https://www.bosterbio.com/catalog/product/view/id/1278032026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41274-mouse-4-1bbl-sds-page.pngMouse recombinant 4-1BBL (4-1BB ligand) protein, AFSDS- PAGE analysis of recombinant mouse 41BBL https://www.bosterbio.com/catalog/product/view/id/1278042026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq04999-mouse-activin-b-sds-page.pngMouse recombinant Activin B protein, AFSDS- PAGE analysis of recombinant mouse Activin B https://www.bosterbio.com/catalog/product/view/id/1278052026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9wu72-mouse-baff-sds-page.pngMouse recombinant BAFF (B-cell activating factor) protein, AFSDS- PAGE analysis of recombinant mouse BAFF https://www.bosterbio.com/catalog/product/view/id/1278062026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01139-3-mouse-beta-ngf-sds-page.pngMouse recombinant beta-NGF (Nerve growth factor-beta) protein, AFSDS- PAGE analysis of recombinant mouse beta-NGF https://www.bosterbio.com/catalog/product/view/id/1278072026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp21275-1-mouse-bmp-4-sds-page.pngMouse recombinant BMP-4 (Bone morphogenetic protein-4) protein, AFSDS- PAGE analysis of recombinant mouse BMP-4 https://www.bosterbio.com/catalog/product/view/id/1278082026-03-10T04:38:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10148-4-mouse-ccl2-sds-page.pngMouse recombinant CCL2 (C-C motif chemokine ligand 2) protein, AFSDS- PAGE analysis of recombinant mouse CCL2 https://www.bosterbio.com/catalog/product/view/id/1278092026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10855-4-mouse-ccl3-sds-page.pngMouse recombinant CCL3 (C-C Motif Chemokine Ligand 3) protein, AFSDS- PAGE analysis of recombinant mouse CCL3 https://www.bosterbio.com/catalog/product/view/id/1278102026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp14097-2-mouse-ccl4-sds-page.pngMouse recombinant CCL4 (C-C Motif Chemokine Ligand 4) protein, AFSDS- PAGE analysis of recombinant mouse CCL4 https://www.bosterbio.com/catalog/product/view/id/1278112026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto55237-mouse-cd27l-sds-page.pngMouse recombinant CD27L (CD27 ligand) protein, AFSDS- PAGE analysis of recombinant mouse CD27L https://www.bosterbio.com/catalog/product/view/id/1278122026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8cc36-6-mouse-cdnf-sds-page.pngMouse recombinant CDNF (Cerebral dopamine neurotrophic factor) protein, AFSDS- PAGE analysis of recombinant mouse CDNF https://www.bosterbio.com/catalog/product/view/id/1278132026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp51642-2-mouse-cntf-sds-page.pngMouse recombinant CNTF (Ciliary neurotrophic factor) protein, AFSDS- PAGE analysis of recombinant mouse CNTF https://www.bosterbio.com/catalog/product/view/id/1278142026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12850-4-mouse-cxcl1-sds-page.pngMouse recombinant CXCL1 (C-C motif chemokine ligand 1) protein, AFSDS- PAGE analysis of recombinant mouse CXCL1 https://www.bosterbio.com/catalog/product/view/id/1278152026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp17515-2-mouse-cxcl10-sds-page.pngMouse recombinant CXCL10 (C-X-C motif chemokine 10) protein, AFSDS- PAGE analysis of recombinant mouse CXCL10 https://www.bosterbio.com/catalog/product/view/id/1278162026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9jhh5-2-mouse-cxcl11-sds-page.pngMouse recombinant CXCL11 (C-X-C motif chemokine 11) protein, AFSDS- PAGE analysis of recombinant mouse CXCL11 https://www.bosterbio.com/catalog/product/view/id/1278172026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp40224-6-mouse-cxcl12-sds-page.pngMouse recombinant CXCL12 (C-X-C motif chemokine 12) protein, AFSDS- PAGE analysis of recombinant mouse CXCL12 https://www.bosterbio.com/catalog/product/view/id/1278182026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8bsu2-1-mouse-cxcl16-sds-page.pngMouse recombinant CXCL16 (C-X-C motif chemokine 16) protein, AFSDS- PAGE analysis of recombinant mouse CXCL16 https://www.bosterbio.com/catalog/product/view/id/1278192026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10889-2-mouse-cxcl2-sds-page.pngMouse recombinant CXCL2 (C-X-C motif chemokine 2) protein, AFSDS- PAGE analysis of recombinant mouse CXCL2 https://www.bosterbio.com/catalog/product/view/id/1278202026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6w5c0-3-mouse-cxcl3-sds-page.pngMouse recombinant CXCL3 (C-X-C motif chemokine 3) protein, AFSDS- PAGE analysis of recombinant mouse CXCL3 https://www.bosterbio.com/catalog/product/view/id/1278212026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp50228-4-mouse-cxcl5-sds-page.pngMouse recombinant CXCL5 (C-X-C motif chemokine 5) protein, AFSDS- PAGE analysis of recombinant mouse CXCL5 https://www.bosterbio.com/catalog/product/view/id/1278222026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9eqi5-mouse-cxcl7-40-113-sds-page.pngMouse recombinant CXCL7 (40-113) (C-X-C motif chemokine 7) protein, AFSDS- PAGE analysis of recombinant mouse CXCL7 (40-113) https://www.bosterbio.com/catalog/product/view/id/1278232026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9eqi5-1-mouse-cxcl7-48-109-sds-page.pngMouse recombinant CXCL7 (48-109) (C-X-C motif chemokine 7) protein, AFSDS- PAGE analysis of recombinant mouse CXCL7 (48-109) https://www.bosterbio.com/catalog/product/view/id/1278242026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp18340-1-mouse-cxcl9-sds-page.pngMouse recombinant CXCL9 (C-X-C motif chemokine 9) protein, AFSDS- PAGE analysis of recombinant mouse CXCL9 https://www.bosterbio.com/catalog/product/view/id/1278252026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01132-7-mouse-egf-sds-page.pngMouse recombinant EGF (Epidermal growth factor) protein, AFSDS- PAGE analysis of recombinant mouse EGF https://www.bosterbio.com/catalog/product/view/id/1278262026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp17182-2-mouse-eno1-sds-page.pngMouse recombinant ENO1 protein, AFSDS- PAGE analysis of recombinant mouse ENO1 https://www.bosterbio.com/catalog/product/view/id/1278272026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp41047-mouse-fasl-sds-page.pngMouse recombinant FasL (Fas ligand) protein, AFSDS- PAGE analysis of recombinant mouse FasL https://www.bosterbio.com/catalog/product/view/id/1278282026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15655-2-mouse-fgf-2-sds-page.pngMouse recombinant FGF-2 (Fibroblast growth factor-basic) protein, AFSDS- PAGE analysis of recombinant mouse FGF-2 https://www.bosterbio.com/catalog/product/view/id/1278292026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9jjn1-5-mouse-fgf-21-sds-page.pngMouse recombinant FGF-21 (Fibroblast growth factor-21) protein, AFSDS- PAGE analysis of recombinant mouse FGF-21 https://www.bosterbio.com/catalog/product/view/id/1278302026-03-10T04:38:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49772-4-mouse-flt-3-ligand-sds-page.pngMouse recombinant Flt-3 Ligand (Fms-related tyrosine kinase-3 ligand) protein, AFSDS- PAGE analysis of recombinant mouse Flt-3 Ligand https://www.bosterbio.com/catalog/product/view/id/1278312026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09920-2-mouse-g-csf-sds-page.pngMouse recombinant G-CSF (Granulocyte colony-stimulating factor) protein, AFSDS- PAGE analysis of recombinant mouse G-CSF https://www.bosterbio.com/catalog/product/view/id/1278322026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp48540-2-mouse-gdnf-sds-page.pngMouse recombinant GDNF (Glial-derived neurotrophic factor) protein, AFSDS- PAGE analysis of recombinant mouse GDNF https://www.bosterbio.com/catalog/product/view/id/1278332026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01587-3-mouse-gm-csf-sds-page.pngMouse recombinant GM-CSF (Granulocyte-macrophage colony-stimulating factor) protein, AFSDS- PAGE analysis of recombinant mouse GM-CSF https://www.bosterbio.com/catalog/product/view/id/1278342026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp51859-mouse-hdgf-sds-page.pngMouse recombinant HDGF (Hepatoma-derived growth factor) protein, AFSDS- PAGE analysis of recombinant mouse HDGF https://www.bosterbio.com/catalog/product/view/id/1278352026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp63158-mouse-hmgb1-sds-page.pngMouse recombinant HMGB1 (High mobility group box 1) protein, AFSDS- PAGE analysis of recombinant mouse HMGB1 https://www.bosterbio.com/catalog/product/view/id/1278362026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01572-mouse-ifn-alpha-1a-sds-page.pngMouse recombinant IFN alpha 1a (Interferon alpha 1a) protein, AFSDS- PAGE analysis of recombinant mouse IFN alpha 1a https://www.bosterbio.com/catalog/product/view/id/1278372026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01575-2-mouse-ifn-beta-1a-sds-page.pngMouse recombinant IFN beta 1a (Interferon beta 1a) protein, AFSDS- PAGE analysis of recombinant mouse IFN beta 1a https://www.bosterbio.com/catalog/product/view/id/1278382026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01580-4-mouse-ifn-gamma-sds-page.pngMouse recombinant IFN gamma (Interferon gamma) protein, AFSDS- PAGE analysis of recombinant mouse IFN gamma https://www.bosterbio.com/catalog/product/view/id/1278392026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp05017-2-mouse-igf-i-sds-page.pngMouse recombinant IGF-I (Insulin-like growth factor-I) protein, AFSDS- PAGE analysis of recombinant mouse IGF-I https://www.bosterbio.com/catalog/product/view/id/1278402026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09535-mouse-igf-ii-sds-page.pngMouse recombinant IGF-II (Insulin-like growth factor-II) protein, AFSDS- PAGE analysis of recombinant mouse IGF-II https://www.bosterbio.com/catalog/product/view/id/1278412026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01582-6-mouse-il-1-alpha-sds-page.pngMouse recombinant IL-1 alpha (Interleukin-1 alpha) protein, AFSDS- PAGE analysis of recombinant mouse IL-1 alpha https://www.bosterbio.com/catalog/product/view/id/1278422026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10749-5-mouse-il-1-beta-sds-page.pngMouse recombinant IL-1 beta (Interleukin-1 beta) protein, AFSDS- PAGE analysis of recombinant mouse IL-1 beta https://www.bosterbio.com/catalog/product/view/id/1278432026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp18893-2-mouse-il-10-sds-page.pngMouse recombinant IL-10 (Interleukin-10) protein, AFSDS- PAGE analysis of recombinant mouse IL-10 https://www.bosterbio.com/catalog/product/view/id/1278442026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp47873-2-mouse-il-11-sds-page.pngMouse recombinant IL-11 (Interleukin-11) protein, AFSDS- PAGE analysis of recombinant mouse IL-11 https://www.bosterbio.com/catalog/product/view/id/1278452026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp43431-1-mouse-il-12-p35-sds-page.pngMouse recombinant IL-12 p35 (Interleukin-12 p35) protein, AFSDS- PAGE analysis of recombinant mouse IL-12 p35 https://www.bosterbio.com/catalog/product/view/id/1278462026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp43432-1-mouse-il-12-p40-sds-page.pngMouse recombinant IL-12 p40 (Interleukin-12 p40) protein, AFSDS- PAGE analysis of recombinant mouse IL-12 p40 https://www.bosterbio.com/catalog/product/view/id/1278472026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp20109-2-mouse-il-13-sds-page.pngMouse recombinant IL-13 (Interleukin-13) protein, AFSDS- PAGE analysis of recombinant mouse IL-13 https://www.bosterbio.com/catalog/product/view/id/1278482026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp48346-4-mouse-il-15-sds-page.pngMouse recombinant IL-15 (Interleukin-15) protein, AFSDS- PAGE analysis of recombinant mouse IL-15 https://www.bosterbio.com/catalog/product/view/id/1278492026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto54824-1-mouse-il-16-sds-page.pngMouse recombinant IL-16 (Interleukin-16) protein, AFSDS- PAGE analysis of recombinant mouse IL-16 https://www.bosterbio.com/catalog/product/view/id/1278502026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq62386-4-mouse-il-17a-sds-page.pngMouse recombinant IL-17A (Interleukin-17A) protein, AFSDS- PAGE analysis of recombinant mouse IL-17A https://www.bosterbio.com/catalog/product/view/id/1278512026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9qxt6-mouse-il-17b-sds-page.pngMouse recombinant IL-17B (Interleukin-17B) protein, AFSDS- PAGE analysis of recombinant mouse IL-17B https://www.bosterbio.com/catalog/product/view/id/1278522026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota0a0b4j1g4-mouse-il-17d-sds-page.pngMouse recombinant IL-17D (Interleukin-17D) protein, AFSDS- PAGE analysis of recombinant mouse IL-17D https://www.bosterbio.com/catalog/product/view/id/1278532026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq7tni7-2-mouse-il-17f-sds-page.pngMouse recombinant IL-17F (Interleukin-17F) protein, AFSDS- PAGE analysis of recombinant mouse IL-17F https://www.bosterbio.com/catalog/product/view/id/1278542026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp70380-4-mouse-il-18-sds-page.pngMouse recombinant IL-18 (Interleukin-18) protein, AFSDS- PAGE analysis of recombinant mouse IL-18 https://www.bosterbio.com/catalog/product/view/id/1278552026-03-10T04:38:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8cj70-1-mouse-il-19-sds-page.pngMouse recombinant IL-19 (Interleukin-19) protein, AFSDS- PAGE analysis of recombinant mouse IL-19 https://www.bosterbio.com/catalog/product/view/id/1278562026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp25085-3-mouse-il-1ra-sds-page.pngMouse recombinant IL-1RA (Interleukin-1 receptor antagonist) protein, AFSDS- PAGE analysis of recombinant mouse IL-1RA https://www.bosterbio.com/catalog/product/view/id/1278572026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp04351-4-mouse-il-2-sds-page.pngMouse recombinant IL-2 (Interleukin-2) protein, AFSDS- PAGE analysis of recombinant mouse IL-2 https://www.bosterbio.com/catalog/product/view/id/1278582026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9jkv9-1-mouse-il-20-sds-page.pngMouse recombinant IL-20 (Interleukin-20) protein, AFSDS- PAGE analysis of recombinant mouse IL-20 https://www.bosterbio.com/catalog/product/view/id/1278592026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9es17-3-mouse-il-21-sds-page.pngMouse recombinant IL-21 (Interleukin-21) protein, AFSDS- PAGE analysis of recombinant mouse IL-21 https://www.bosterbio.com/catalog/product/view/id/1278602026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9jjy9-4-mouse-il-22-sds-page.pngMouse recombinant IL-22 (Interleukin-22) protein, AFSDS- PAGE analysis of recombinant mouse IL-22 https://www.bosterbio.com/catalog/product/view/id/1278612026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq925s4-mouse-il-24-sds-page.pngMouse recombinant IL-24 (Interleukin-24) protein, AFSDS- PAGE analysis of recombinant mouse IL-24 https://www.bosterbio.com/catalog/product/view/id/1278622026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8vhh8-1-mouse-il-25-sds-page.pngMouse recombinant IL-25 (Interleukin-25) protein, AFSDS- PAGE analysis of recombinant mouse IL-25 https://www.bosterbio.com/catalog/product/view/id/1278632026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto35228-1-mouse-il-27-ebi3-sds-page.pngMouse recombinant IL-27 EBI3 (Interleukin-27 EBI3) protein, AFSDS- PAGE analysis of recombinant mouse IL-27 EBI3 https://www.bosterbio.com/catalog/product/view/id/1278642026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq4vk74-2-mouse-il-28a-sds-page.pngMouse recombinant IL-28A (Interleukin-28A) protein, AFSDS- PAGE analysis of recombinant mouse IL-28A https://www.bosterbio.com/catalog/product/view/id/1278652026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8cgk6-1-mouse-il-28b-sds-page.pngMouse recombinant IL-28B (Interleukin-28B) protein, AFSDS- PAGE analysis of recombinant mouse IL-28B https://www.bosterbio.com/catalog/product/view/id/1278662026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01586-4-mouse-il-3-sds-page.pngMouse recombinant IL-3 (Interleukin-3) protein, AFSDS- PAGE analysis of recombinant mouse IL-3 https://www.bosterbio.com/catalog/product/view/id/1278672026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8k3i6-1-mouse-il-30-sds-page.pngMouse recombinant IL-30 (Interleukin-30) protein, AFSDS- PAGE analysis of recombinant mouse IL-30 https://www.bosterbio.com/catalog/product/view/id/1278682026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq6eal8-2-mouse-il-31-sds-page.pngMouse recombinant IL-31 (Interleukin-31) protein, AFSDS- PAGE analysis of recombinant mouse IL-31 https://www.bosterbio.com/catalog/product/view/id/1278692026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8bvz5-4-mouse-il-33-sds-page.pngMouse recombinant IL-33 (Interleukin-33) protein, AFSDS- PAGE analysis of recombinant mouse IL-33 https://www.bosterbio.com/catalog/product/view/id/1278702026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8r1r4-2-mouse-il-34-sds-page.pngMouse recombinant IL-34 (Interleukin-34) protein, AFSDS- PAGE analysis of recombinant mouse IL-34 https://www.bosterbio.com/catalog/product/view/id/1278712026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9jla2-4-mouse-il-36-alpha-sds-page.pngMouse recombinant IL-36 alpha (Interleukin-36 alpha) protein, AFSDS- PAGE analysis of recombinant mouse IL-36 alpha https://www.bosterbio.com/catalog/product/view/id/1278722026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8r460-1-mouse-il-36-gamma-sds-page.pngMouse recombinant IL-36 gamma (Interleukin-36 gamma) protein, AFSDS- PAGE analysis of recombinant mouse IL-36 gamma https://www.bosterbio.com/catalog/product/view/id/1278732026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9qyy1-2-mouse-il-36-ra-sds-page.pngMouse recombinant IL-36RA (Interleukin-36 receptor antagonist) protein, AFSDS- PAGE analysis of recombinant mouse IL-36RA https://www.bosterbio.com/catalog/product/view/id/1278742026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq8r459-mouse-il-38-sds-page.pngMouse recombinant IL-38 (Interleukin-38) protein, AFSDS- PAGE analysis of recombinant mouse IL-38 https://www.bosterbio.com/catalog/product/view/id/1278752026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07750-2-mouse-il-4-sds-page.pngMouse recombinant IL-4 (Interleukin-4) protein, AFSDS- PAGE analysis of recombinant mouse IL-4 https://www.bosterbio.com/catalog/product/view/id/1278762026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp04401-4-mouse-il-5-sds-page.pngMouse recombinant IL-5 (Interleukin-5) protein, AFSDS- PAGE analysis of recombinant mouse IL-5 https://www.bosterbio.com/catalog/product/view/id/1278772026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp08505-6-mouse-il-6-sds-page.pngMouse recombinant IL-6 (Interleukin-6) protein, AFSDS- PAGE analysis of recombinant mouse IL-6 https://www.bosterbio.com/catalog/product/view/id/1278782026-03-10T04:38:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp10168-2-mouse-il-7-sds-page.pngMouse recombinant IL-7 (Interleukin-7) protein, AFSDS- PAGE analysis of recombinant mouse IL-7 https://www.bosterbio.com/catalog/product/view/id/1278792026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp15247-2-mouse-il-9-sds-page.pngMouse recombinant IL-9 (Interleukin-9) protein, AFSDS- PAGE analysis of recombinant mouse IL-9 https://www.bosterbio.com/catalog/product/view/id/1278802026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09056-1-mouse-lif-sds-page.pngMouse recombinant LIF protein, AFSDS- PAGE analysis of recombinant mouse LIF https://www.bosterbio.com/catalog/product/view/id/1278812026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9qyh9-2-mouse-light-sds-page.pngMouse recombinant LIGHT protein, AFSDS- PAGE analysis of recombinant mouse LIGHT https://www.bosterbio.com/catalog/product/view/id/1278822026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07141-3-mouse-m-csf-sds-page.pngMouse recombinant M-CSF (Macrophage colony-stimulating factor) protein, AFSDS- PAGE analysis of recombinant mouse M-CSF https://www.bosterbio.com/catalog/product/view/id/1278832026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp12025-2-mouse-midkine-sds-page.pngMouse recombinant Midkine protein, AFSDS- PAGE analysis of recombinant mouse Midkine https://www.bosterbio.com/catalog/product/view/id/1278842026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp34884-3-mouse-mif-sds-page.pngMouse recombinant MIF (Macrophage migration inhibitory factor) protein, AFSDS- PAGE analysis of recombinant mouse MIF https://www.bosterbio.com/catalog/product/view/id/1278852026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp97463-mouse-neurturin-sds-page.pngMouse recombinant Neurturin protein, AFSDS- PAGE analysis of recombinant mouse Neurturin https://www.bosterbio.com/catalog/product/view/id/1278862026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp43488-1-mouse-ox40l-sds-page.pngMouse recombinant OX40L protein, AFSDS- PAGE analysis of recombinant mouse OX40L https://www.bosterbio.com/catalog/product/view/id/1278872026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto35235-4-mouse-rankl-sds-page.pngMouse recombinant RANKL (Receptor activator of nuclear factor kappa-Β ligand) protein, AFSDS- PAGE analysis of recombinant mouse RANKL https://www.bosterbio.com/catalog/product/view/id/1278882026-04-01T05:01:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp04202-2-mouse-tgf-beta-1-sds-page.pngMouse recombinant TGF beta 1 (Transforming growth factor beta 1) protein, AFSDS- PAGE analysis of recombinant mouse TGF beta 1 https://www.bosterbio.com/catalog/product/view/id/1278892026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp06804-6-mouse-tnf-alpha-sds-page.pngMouse recombinant TNF alpha (Tumor necrosis factor alpha) protein, AFSDS- PAGE analysis of recombinant mouse TNF alpha https://www.bosterbio.com/catalog/product/view/id/1278902026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09225-mouse-tnf-beta-sds-page.pngMouse recombinant TNF beta (Tumor necrosis factor beta) protein, AFSDS- PAGE analysis of recombinant mouse TNF beta https://www.bosterbio.com/catalog/product/view/id/1278912026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp50592-2-mouse-trail-sds-page.pngMouse recombinant TRAIL (TNF-related apoptosis-inducing ligand) protein, AFSDS- PAGE analysis of recombinant mouse TRAIL https://www.bosterbio.com/catalog/product/view/id/1278922026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto54907-mouse-tweak-sds-page.pngMouse recombinant TWEAK (TNF-related weak inducer of apoptosis) protein, AFSDS- PAGE analysis of recombinant mouse TWEAK https://www.bosterbio.com/catalog/product/view/id/1278932026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq00731-6-mouse-vegf121-sds-page.pngMouse recombinant VEGF121 (Vascular endothelial growth factor 121) protein, AFSDS- PAGE analysis of recombinant mouse VEGF121 https://www.bosterbio.com/catalog/product/view/id/1278942026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq00731-7-mouse-vegf165-sds-page.pngMouse recombinant VEGF165 (Vascular endothelial growth factor 165) protein, AFSDS- PAGE analysis of recombinant mouse VEGF165 https://www.bosterbio.com/catalog/product/view/id/1278952026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota7ljt9-swine-bmp-4-sds-page.pngSwine recombinant BMP-4 (Bone morphogenetic protein-4) protein, AFSDS- PAGE analysis of recombinant swine BMP-4 https://www.bosterbio.com/catalog/product/view/id/1278962026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp42831-swine-ccl2-sds-page.pngSwine recombinant CCL2 (C-C Motif Chemokine Ligand 2) protein, AFSDS- PAGE analysis of recombinant swine CCL2 https://www.bosterbio.com/catalog/product/view/id/1278972026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq5s1s3-swine-cxcl10-sds-page.pngSwine recombinant CXCL10 (C-X-C motif chemokine 10) protein, AFSDS- PAGE analysis of recombinant swine CXCL10 https://www.bosterbio.com/catalog/product/view/id/1278982026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota0a4x1sx03-swine-cxcl11-sds-page.pngSwine recombinant CXCL11 (C-X-C motif chemokine 11) protein, AFSDS- PAGE analysis of recombinant swine CXCL11 https://www.bosterbio.com/catalog/product/view/id/1278992026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota0a287a706-swine-cxcl13-sds-page.pngSwine recombinant CXCL13 (C-X-C motif chemokine 13) protein, AFSDS- PAGE analysis of recombinant swine CXCL13 https://www.bosterbio.com/catalog/product/view/id/1279002026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protb0fyk2-swine-cxcl9-sds-page.pngSwine recombinant CXCL9 (C-X-C motif chemokine 9) protein, AFSDS- PAGE analysis of recombinant swine CXCL9 https://www.bosterbio.com/catalog/product/view/id/1279012026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq00968-swine-egf-sds-page.pngSwine recombinant EGF (Epidermal growth factor) protein, AFSDS- PAGE analysis of recombinant swine EGF https://www.bosterbio.com/catalog/product/view/id/1279022026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/prota0a287bgk8-swine-fgf-2-sds-page.pngSwine recombinant FGF-2 (Fibroblast growth factor-2) protein, AFSDS- PAGE analysis of recombinant swine FGF-2 https://www.bosterbio.com/catalog/product/view/id/1279032026-03-10T04:38:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protd2k7d6-swine-flt-3-ligand-sds-page.pngSwine recombinant Flt-3 Ligand (Fms-related tyrosine kinase-3 ligand) protein, AFSDS- PAGE analysis of recombinant swine Flt-3 Ligand https://www.bosterbio.com/catalog/product/view/id/1279042026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq29118-1-swine-gm-csf-sds-page.pngSwine recombinant GM-CSF (Granulocyte-macrophage colony-stimulating factor) protein, AFSDS- PAGE analysis of recombinant swine GM-CSF https://www.bosterbio.com/catalog/product/view/id/1279052026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp17803-swine-ifn-gamma-sds-page.pngSwine recombinant IFN gamma (Interferon gamma) protein, AFSDS- PAGE analysis of recombinant swine IFN gamma https://www.bosterbio.com/catalog/product/view/id/1279062026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp16545-swine-igf-i-sds-page.pngSwine recombinant IGF-I (Insulin-like growth factor-I) protein, AFSDS- PAGE analysis of recombinant swine IGF-I https://www.bosterbio.com/catalog/product/view/id/1279072026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp18430-1-swine-il-1-alpha-sds-page.pngSwine recombinant IL-1 alpha (Interleukin-1 alpha) protein, AFSDS- PAGE analysis of recombinant swine IL-1 alpha https://www.bosterbio.com/catalog/product/view/id/1279082026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26889-1-swine-il-1-beta-sds-page.pngSwine recombinant IL-1 beta (Interleukin-1 beta) protein, AFSDS- PAGE analysis of recombinant swine IL-1 beta https://www.bosterbio.com/catalog/product/view/id/1279092026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq29055-swine-il-10-sds-page.pngSwine recombinant IL-10 (Interleukin-10) protein, AFSDS- PAGE analysis of recombinant swine IL-10 https://www.bosterbio.com/catalog/product/view/id/1279102026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq95253-swine-il-15-sds-page.pngSwine recombinant IL-15 (Interleukin-15) protein, AFSDS- PAGE analysis of recombinant swine IL-15 https://www.bosterbio.com/catalog/product/view/id/1279112026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protb6e279-swine-il-17a-sds-page.pngSwine recombinant IL-17A (Interleukin-17A) protein, AFSDS- PAGE analysis of recombinant swine IL-17A https://www.bosterbio.com/catalog/product/view/id/1279122026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26891-1-swine-il-2-sds-page.pngSwine recombinant IL-2 (Interleukin-2) protein, AFSDS- PAGE analysis of recombinant swine IL-2 https://www.bosterbio.com/catalog/product/view/id/1279132026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq04745-swine-il-4-sds-page.pngSwine recombinant IL-4 (Interleukin-4) protein, AFSDS- PAGE analysis of recombinant swine IL-4 https://www.bosterbio.com/catalog/product/view/id/1279142026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26893-swine-il-6-sds-page.pngSwine recombinant IL-6 (Interleukin-6) protein, AFSDS- PAGE analysis of recombinant swine IL-6 https://www.bosterbio.com/catalog/product/view/id/1279152026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp26894-1-swine-il-8-sds-page.pngSwine recombinant IL-8 (Interleukin-8) protein, AFSDS- PAGE analysis of recombinant swine IL-8 https://www.bosterbio.com/catalog/product/view/id/1279162026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp07200-swine-tgf-beta-1-sds-page.pngSwine recombinant TGF beta 1 (Transforming growth factor beta 1) protein, AFSDS- PAGE analysis of recombinant swine TGF beta 1 https://www.bosterbio.com/catalog/product/view/id/1279172026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp23563-1-swine-tnf-alpha-sds-page.pngSwine recombinant TNF alpha (Tumor necrosis factor alpha) protein, AFSDS- PAGE analysis of recombinant swine TNF alpha https://www.bosterbio.com/catalog/product/view/id/1279182026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49151-swine-vegf-sds-page.pngSwine recombinant VEGF (Vascular endothelial growth factor) protein, AFSDS- PAGE analysis of recombinant swine VEGF https://www.bosterbio.com/catalog/product/view/id/1279202026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/proto95998-4-il-18bp-sds-page.pngHuman recombinant IL-18BP (Interleukin-18-binding protein) protein, AFSDS- PAGE analysis of recombinant human IL-18BP https://www.bosterbio.com/catalog/product/view/id/1279242026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp97466-2-mouse-noggin-sds-page.pngMouse recombinant Noggin protein, AFSDS- PAGE analysis of recombinant mouse Noggin https://www.bosterbio.com/catalog/product/view/id/1279252026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp09038-10-fgf-2-tag-free-sds-page.pngHuman recombinant FGF-2 (Fibroblast Growth Factors 2) protein, AF, Tag freeSDS- PAGE analysis of recombinant human FGF-2, Tag free https://www.bosterbio.com/catalog/product/view/id/1279272026-03-10T04:38:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01137-10-tgf-beta-1-hek293-sds-page.pngHuman recombinant TGF beta 1 (Transforming growth factor beta 1) protein, AFSDS- PAGE analysis of recombinant human TGF beta 1 https://www.bosterbio.com/catalog/product/view/id/1279342026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01579-10-gmp-human-ifn-gamma-sds-page.pngHuman recombinant IFN gamma protein, GMPSDS- PAGE analysis of GMP human IFN gamma https://www.bosterbio.com/catalog/product/view/id/1279352026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01584-6-gmp-human-il-1-beta-sds-page.pngHuman recombinant IL-1 beta protein, GMPSDS- PAGE analysis of GMP human IL-1 beta https://www.bosterbio.com/catalog/product/view/id/1279372026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp40933-6-gmp-human-il-15-sds-page.pngHuman recombinant IL-15 protein, GMPSDS- PAGE analysis of GMP human IL-15 https://www.bosterbio.com/catalog/product/view/id/1279382026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq14116-3-gmp-human-il-18-sds-page.pngHuman recombinant IL-18 protein, GMPSDS- PAGE analysis of GMP human IL-18 https://www.bosterbio.com/catalog/product/view/id/1279392026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp60568-7-gmp-human-il-2-sds-page.pngHuman recombinant IL-2 protein, GMPSDS- PAGE analysis of GMP human IL-2 https://www.bosterbio.com/catalog/product/view/id/1279402026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protq9hbe4-6-gmp-human-il-21-sds-page.pngHuman recombinant IL-21 protein, GMPSDS- PAGE analysis of GMP human IL-21 https://www.bosterbio.com/catalog/product/view/id/1279442026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp13232-10-gmp-human-il-7-sds-page.pngHuman recombinant IL-7 protein, GMPSDS- PAGE analysis of GMP human IL-7 https://www.bosterbio.com/catalog/product/view/id/1279472026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp01375-9-gmp-human-tnf-alpha-sds-page.pngHuman recombinant TNF alpha protein, GMPSDS- PAGE analysis of GMP human TNF alpha https://www.bosterbio.com/catalog/product/view/id/1279512026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1953_1.pngHuman CHRDL1 PicoKine® Quick ELISA KitHuman CHRDL1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1279522026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0369_1.pngHuman HGF/Hepatocyte growth factor PicoKine® Quick ELISA KitHuman HGF PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1279532026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0349_1.pngHuman Fibronectin PicoKine® Quick ELISA KitHuman Fibronectin PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1279592026-03-10T04:38:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek1384_1.pngMouse ADAMTS1 PicoKine® Quick ELISA KitMouse ADAMTS1 PicoKine ELISA Kit standard curve https://www.bosterbio.com/picokine-elisa-kits/mouse-tnf-beta-picokine-trade-elisa-kit-ek0585-boster.html2026-03-10T04:38:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/k/ek0585_2_1.pngMouse TNF beta ELISA Kit PicoKine®Mouse TNF Beta PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1279612026-03-10T04:38:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0651_2.pngHuman AFP/Alpha-fetoprotein PicoKine® Quick ELISA KitHuman AFP PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1279632026-03-10T04:38:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0862_1.pngMouse PTX3/Pentraxin 3 PicoKine® Quick ELISA KitMouse PTX3/Pentraxin 3 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1279642026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09529-2-nle1-primary-antibodies-wb-testing-1.jpgAnti-NLE1 Antibody Picoband® Western blot analysis of NLE1 using anti-NLE1 antibody (A09529-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat ovary tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse ovary tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NLE1 antigen affinity purified polyclonal antibody (A09529-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NLE1 at approximately 45 kDa. The expected band size for NLE1 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09529-2-nle1-primary-antibodies-fcm-testing-2.jpgAnti-NLE1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NLE1 antibody (A09529-2). Overlay histogram showing 293T cells stained with A09529-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NLE1 Antibody (A09529-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279652026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04591-1-creb3l2-primary-antibodies-wb-testing-1.jpgAnti-CREB3L2 Antibody Picoband® Western blot analysis of CREB3L2 using anti-CREB3L2 antibody (A04591-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human HUVEC whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CREB3L2 antigen affinity purified polyclonal antibody (A04591-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CREB3L2 at approximately 60 kDa. The expected band size for CREB3L2 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04591-1-creb3l2-primary-antibodies-ihc-testing-2.jpgAnti-CREB3L2 Antibody Picoband® IHC analysis of CREB3L2 using anti-CREB3L2 antibody (A04591-1). CREB3L2 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CREB3L2 Antibody (A04591-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04591-1-creb3l2-primary-antibodies-if-testing-3.jpgAnti-CREB3L2 Antibody Picoband® IF analysis of CREB3L2 using anti-CREB3L2 antibody (A04591-1). CREB3L2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CREB3L2 Antibody (A04591-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04591-1-creb3l2-primary-antibodies-fcm-testing-4.jpgAnti-CREB3L2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-CREB3L2 antibody (A04591-1). Overlay histogram showing HEL cells stained with A04591-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CREB3L2 Antibody (A04591-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279662026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13404-3-nsun6-primary-antibodies-wb-testing-1.jpgAnti-NSUN6 Antibody Picoband® Western blot analysis of NSUN6 using anti-NSUN6 antibody (A13404-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat PC-12 whole cell lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSUN6 antigen affinity purified polyclonal antibody (A13404-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSUN6 at approximately 52 kDa. The expected band size for NSUN6 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13404-3-nsun6-primary-antibodies-ihc-testing-2.jpgAnti-NSUN6 Antibody Picoband® IHC analysis of NSUN6 using anti-NSUN6 antibody (A13404-3). NSUN6 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NSUN6 Antibody (A13404-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13404-3-nsun6-primary-antibodies-fcm-testing-3.jpgAnti-NSUN6 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-NSUN6 antibody (A13404-3). Overlay histogram showing 293T cells stained with A13404-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSUN6 Antibody (A13404-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279672026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08723-1-txndc3-nme8-primary-antibodies-wb-testing-1.jpgAnti-TXNDC3/NME8 Antibody Picoband® Western blot analysis of TXNDC3/NME8 using anti-TXNDC3/NME8 antibody (A08723-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat spleen tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TXNDC3/NME8 antigen affinity purified polyclonal antibody (A08723-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TXNDC3/NME8 at approximately 67 kDa. The expected band size for TXNDC3/NME8 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08723-1-txndc3-nme8-primary-antibodies-fcm-testing-2.jpgAnti-TXNDC3/NME8 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-TXNDC3/NME8 antibody (A08723-1). Overlay histogram showing HEL cells stained with A08723-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TXNDC3/NME8 Antibody (A08723-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279682026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14267-nsun7-primary-antibodies-wb-testing-1.jpgAnti-NSUN7 Antibody Picoband® Western blot analysis of NSUN7 using anti-NSUN7 antibody (A14267). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U2OS whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: rat testis tissue lysates, Lane 4: rat RH-35 whole cell lysates, Lane 5: mouse liver tissue lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSUN7 antigen affinity purified polyclonal antibody (A14267) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSUN7 at approximately 81 kDa. The expected band size for NSUN7 is at 81 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14267-nsun7-primary-antibodies-fcm-testing-2.jpgAnti-NSUN7 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-NSUN7 antibody (A14267). Overlay histogram showing PC-3 cells stained with A14267 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSUN7 Antibody (A14267, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279692026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06286-3-nprl2-primary-antibodies-wb-testing-1.jpgAnti-NPRL2 Antibody Picoband® Western blot analysis of NPRL2 using anti-NPRL2 antibody (A06286-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat skeletal muscle tissue lysates, Lane 2: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NPRL2 antigen affinity purified polyclonal antibody (A06286-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NPRL2 at approximately 48 kDa. The expected band size for NPRL2 is at 44 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06286-3-nprl2-primary-antibodies-fcm-testing-2.jpgAnti-NPRL2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NPRL2 antibody (A06286-3). Overlay histogram showing HEL cells stained with A06286-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NPRL2 Antibody (A06286-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279702026-03-17T05:16:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15219-otud6b-primary-antibodies-wb-testing-1.jpgAnti-OTUD6B Antibody Picoband® Western blot analysis of OTUD6B using anti-OTUD6B antibody (A15219). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human MCF-7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-OTUD6B antigen affinity purified polyclonal antibody (A15219) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for OTUD6B at approximately 36 kDa. The expected band size for OTUD6B is at 34 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a15219-otud6b-primary-antibodies-fcm-testing-2.jpgAnti-OTUD6B Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-OTUD6B antibody (A15219). Overlay histogram showing 293T cells stained with A15219 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-OTUD6B Antibody (A15219, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279712026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07479-1-cep110-cntrl-primary-antibodies-wb-testing-1.jpgAnti-CEP110/CNTRL Antibody Picoband® Western blot analysis of CEP110/CNTRL using anti-CEP110/CNTRL antibody (A07479-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CEP110/CNTRL antigen affinity purified polyclonal antibody (A07479-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CEP110/CNTRL at approximately 269 kDa. The expected band size for CEP110/CNTRL is at 269 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07479-1-cep110-cntrl-primary-antibodies-fcm-testing-2.jpgAnti-CEP110/CNTRL Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-CEP110/CNTRL antibody (A07479-1). Overlay histogram showing HEL cells stained with A07479-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CEP110/CNTRL Antibody (A07479-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279722026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06687-2-sharpin-primary-antibodies-wb-testing-1.jpgAnti-SHARPIN Antibody Picoband® Western blot analysis of SHARPIN using anti-SHARPIN antibody (A06687-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SHARPIN antigen affinity purified polyclonal antibody (A06687-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for SHARPIN at approximately 40 kDa. The expected band size for SHARPIN is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06687-2-sharpin-primary-antibodies-ihc-testing-2.jpgAnti-SHARPIN Antibody Picoband® IHC analysis of SHARPIN using anti-SHARPIN antibody (A06687-2). SHARPIN was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-SHARPIN Antibody (A06687-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06687-2-sharpin-primary-antibodies-fcm-testing-3.jpgAnti-SHARPIN Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-SHARPIN antibody (A06687-2). Overlay histogram showing A549 cells stained with A06687-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SHARPIN Antibody (A06687-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279732026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03545-3-cyp7b1-primary-antibodies-wb-testing-1.jpgAnti-CYP7B1 Antibody Picoband® Western blot analysis of CYP7B1 using anti-CYP7B1 antibody (A03545-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYP7B1 antigen affinity purified polyclonal antibody (A03545-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CYP7B1 at approximately 58 kDa. The expected band size for CYP7B1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03545-3-cyp7b1-primary-antibodies-ihc-testing-2.jpgAnti-CYP7B1 Antibody Picoband® IHC analysis of CYP7B1 using anti-CYP7B1 antibody (A03545-3). CYP7B1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CYP7B1 Antibody (A03545-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03545-3-cyp7b1-primary-antibodies-fcm-testing-3.jpgAnti-CYP7B1 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-CYP7B1 antibody (A03545-3). Overlay histogram showing THP-1 cells stained with A03545-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CYP7B1 Antibody (A03545-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279742026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01145-2-dbt-primary-antibodies-wb-testing-1.jpgAnti-DBT Antibody Picoband® Western blot analysis of DBT using anti-DBT antibody (A01145-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat stomach tissue lysates, Lane 6: rat kidney tissue lysates, Lane 7: mouse stomach tissue lysates, Lane 8: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DBT antigen affinity purified polyclonal antibody (A01145-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DBT at approximately 53 kDa. The expected band size for DBT is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01145-2-dbt-primary-antibodies-if-testing-2.jpgAnti-DBT Antibody Picoband® IF analysis of DBT using anti-DBT antibody (A01145-2) and anti-Beta Tubulin antibody (M01857-3). DBT was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DBT Antibody (A01145-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®550 Conjugated Goat Anti-Mouse IgG (BA1133) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01145-2-dbt-primary-antibodies-ip-testing-3.jpgAnti-DBT Antibody Picoband® Immunoprecipitating DBT in A431 whole cell lysate. Western blot analysis of DBT using anti-DBT antibody (A01145-2). Lane 1: A431 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-DBT antibody in A431 whole cell lysate, Lane 3: anti-DBT antibody (2μg) + A431 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-DBT antigen affinity purified polyclonal antibody (A01145-2) at a dilution of 0.5 μg/mL and probed with a mouse anti-rabbit IgG-HRP secondary antibody (Light Chain). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for DBT at approximately 53 kDa. The expected band size for DBT is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01145-2-dbt-primary-antibodies-fcm-testing-4.jpgAnti-DBT Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-DBT antibody (A01145-2). Overlay histogram showing SiHa cells stained with A01145-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DBT Antibody (A01145-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279752026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03811-2-depdc6-deptor-primary-antibodies-wb-testing-1.jpgAnti-DEPDC6/DEPTOR Antibody Picoband® Western blot analysis of DEPDC6/DEPTOR using anti-DEPDC6/DEPTOR antibody (A03811-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human RT4 whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: rat skeletal muscle tissue lysates, Lane 7: mouse heart tissue lysates, Lane 8: mouse skeletal muscle tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DEPDC6/DEPTOR antigen affinity purified polyclonal antibody (A03811-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for DEPDC6/DEPTOR at approximately 48 kDa. The expected band size for DEPDC6/DEPTOR is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03811-2-depdc6-deptor-primary-antibodies-ihc-testing-2.jpgAnti-DEPDC6/DEPTOR Antibody Picoband® IHC analysis of DEPDC6/DEPTOR using anti-DEPDC6/DEPTOR antibody (A03811-2). DEPDC6/DEPTOR was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DEPDC6/DEPTOR Antibody (A03811-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03811-2-depdc6-deptor-primary-antibodies-ihc-testing-3.jpgAnti-DEPDC6/DEPTOR Antibody Picoband® IHC analysis of DEPDC6/DEPTOR using anti-DEPDC6/DEPTOR antibody (A03811-2). DEPDC6/DEPTOR was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DEPDC6/DEPTOR Antibody (A03811-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03811-2-depdc6-deptor-primary-antibodies-fcm-testing-4.jpgAnti-DEPDC6/DEPTOR Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-DEPDC6/DEPTOR antibody (A03811-2). Overlay histogram showing MCF-7 cells stained with A03811-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DEPDC6/DEPTOR Antibody (A03811-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279762026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00983-1-crbn-primary-antibodies-wb-testing-1.jpgAnti-CRBN Antibody Picoband® Western blot analysis of CRBN using anti-CRBN antibody (A00983-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse brain tissue lysates, Lane 7: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CRBN antigen affinity purified polyclonal antibody (A00983-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CRBN at approximately 51 kDa. The expected band size for CRBN is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00983-1-crbn-primary-antibodies-if-testing-2.jpgAnti-CRBN Antibody Picoband® IF analysis of CRBN using anti-CRBN antibody (A00983-1). CRBN was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CRBN Antibody (A00983-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00983-1-crbn-primary-antibodies-fcm-testing-3.jpgAnti-CRBN Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-CRBN antibody (A00983-1). Overlay histogram showing 293T cells stained with A00983-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CRBN Antibody (A00983-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279772026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07567-1-nav3-primary-antibodies-wb-testing-1.jpgAnti-NAV3 Antibody Picoband® Western blot analysis of NAV3 using anti-NAV3 antibody (A07567-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U251 whole cell lysates, Lane 2: human HUVEC whole cell lysates, Lane 3: human SH-SY5Y whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAV3 antigen affinity purified polyclonal antibody (A07567-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAV3 at approximately 256 kDa. The expected band size for NAV3 is at 256 kDa. https://www.bosterbio.com/catalog/product/view/id/1279782026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09560-nsmaf-primary-antibodies-wb-testing-1.jpgAnti-NSMAF Antibody Picoband® Western blot analysis of NSMAF using anti-NSMAF antibody (A09560). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human HEL whole cell lysates, Lane 4: rat thymus tissue lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSMAF antigen affinity purified polyclonal antibody (A09560) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSMAF at approximately 104 kDa. The expected band size for NSMAF is at 104 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09560-nsmaf-primary-antibodies-fcm-testing-2.jpgAnti-NSMAF Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NSMAF antibody (A09560). Overlay histogram showing HEL cells stained with A09560 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NSMAF Antibody (A09560, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279792026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13426-1-nudt12-primary-antibodies-wb-testing-1.jpgAnti-NUDT12 Antibody Picoband® Western blot analysis of NUDT12 using anti-NUDT12 antibody (A13426-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: rat liver tissue lysates, Lane 4: mouse liver tissue lysates, Lane 5: mouse Hepa1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT12 antigen affinity purified polyclonal antibody (A13426-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDT12 at approximately 47 kDa. The expected band size for NUDT12 is at 52 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13426-1-nudt12-primary-antibodies-fcm-testing-2.jpgAnti-NUDT12 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-NUDT12 antibody (A13426-1). Overlay histogram showing A549 cells stained with A13426-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDT12 Antibody (A13426-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279802026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02873-3-nab2-primary-antibodies-wb-testing-1.jpgAnti-NAB2 Antibody Picoband® Western blot analysis of NAB2 using anti-NAB2 antibody (A02873-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human SiHa whole cell lysates, Lane 3: rat thymus tissue lysates, Lane 4: mouse thymus tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAB2 antigen affinity purified polyclonal antibody (A02873-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAB2 at approximately 57 kDa. The expected band size for NAB2 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02873-3-nab2-primary-antibodies-if-testing-2.jpgAnti-NAB2 Antibody Picoband® IF analysis of NAB2 using anti-NAB2 antibody (A02873-3) and anti-Beta Tubulin antibody (M01857-3). NAB2 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NAB2 Antibody (A02873-3) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02873-3-nab2-primary-antibodies-fcm-testing-3.jpgAnti-NAB2 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-NAB2 antibody (A02873-3). Overlay histogram showing MCF-7 cells stained with A02873-3 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAB2 Antibody (A02873-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279812026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32428-1-pycrl-pycr3-primary-antibodies-wb-testing-1.jpgAnti-PYCRL/PYCR3 Antibody Picoband® Western blot analysis of PYCRL/PYCR3 using anti-PYCRL/PYCR3 antibody (A32428-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: mouse kidney tissue lysates, Lane 6: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PYCRL/PYCR3 antigen affinity purified polyclonal antibody (A32428-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for PYCRL/PYCR3 at approximately 29 kDa. The expected band size for PYCRL/PYCR3 is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32428-1-pycrl-pycr3-primary-antibodies-fcm-testing-2.jpgAnti-PYCRL/PYCR3 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-PYCRL/PYCR3 antibody (A32428-1). Overlay histogram showing A549 cells stained with A32428-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PYCRL/PYCR3 Antibody (A32428-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279822026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03549-naglu-primary-antibodies-wb-testing-1.jpgAnti-NAGLU Antibody Picoband® Western blot analysis of NAGLU using anti-NAGLU antibody (A03549). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAGLU antigen affinity purified polyclonal antibody (A03549) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAGLU at approximately 82 kDa. The expected band size for NAGLU is at 82 kDa. https://www.bosterbio.com/catalog/product/view/id/1279832026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08540-2-nans-primary-antibodies-wb-testing-1.jpgAnti-NANS Antibody Picoband® Western blot analysis of NANS using anti-NANS antibody (A08540-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: rat liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NANS antigen affinity purified polyclonal antibody (A08540-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NANS at approximately 38 kDa. The expected band size for NANS is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08540-2-nans-primary-antibodies-if-testing-2.jpgAnti-NANS Antibody Picoband® IF analysis of NANS using anti-NANS antibody (A08540-2). NANS was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NANS Antibody (A08540-2) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1279842026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17289-nap1l3-primary-antibodies-wb-testing-1.jpgAnti-NAP1L3 Antibody Picoband® Western blot analysis of NAP1L3 using anti-NAP1L3 antibody (A17289). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U2OS whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NAP1L3 antigen affinity purified polyclonal antibody (A17289) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NAP1L3 at approximately 58 kDa. The expected band size for NAP1L3 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17289-nap1l3-primary-antibodies-fcm-testing-2.jpgAnti-NAP1L3 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-NAP1L3 antibody (A17289). Overlay histogram showing HEL cells stained with A17289 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NAP1L3 Antibody (A17289, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279852026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32387-narfl-ciao3-primary-antibodies-wb-testing-1.jpgAnti-NARFL/CIAO3 Antibody Picoband® Western blot analysis of NARFL/CIAO3 using anti-NARFL/CIAO3 antibody (A32387). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NARFL/CIAO3 antigen affinity purified polyclonal antibody (A32387) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NARFL/CIAO3 at approximately 53 kDa. The expected band size for NARFL/CIAO3 is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a32387-narfl-ciao3-primary-antibodies-fcm-testing-2.jpgAnti-NARFL/CIAO3 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-NARFL/CIAO3 antibody (A32387). Overlay histogram showing MCF-7 cells stained with A32387 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-NARFL/CIAO3 Antibody (A32387, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279862026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19531-1-ttc34-primary-antibodies-wb-testing-1.jpgAnti-TTC34 Antibody Picoband® Western blot analysis of TTC34 using anti-TTC34 antibody (A19531-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: rat PC-12 whole cell lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse testis tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TTC34 antigen affinity purified polyclonal antibody (A19531-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for TTC34 at approximately 61 kDa. The expected band size for TTC34 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19531-1-ttc34-primary-antibodies-ihc-testing-2.jpgAnti-TTC34 Antibody Picoband® IHC analysis of TTC34 using anti-TTC34 antibody (A19531-1). TTC34 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TTC34 Antibody (A19531-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19531-1-ttc34-primary-antibodies-if-testing-3.jpgAnti-TTC34 Antibody Picoband® IF analysis of TTC34 using anti-TTC34 antibody (A19531-1) and anti-Beta Tubulin antibody (M01857-3). TTC34 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TTC34 Antibody (A19531-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19531-1-ttc34-primary-antibodies-fcm-testing-4.jpgAnti-TTC34 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-TTC34 antibody (A19531-1). Overlay histogram showing Jurkat cells stained with A19531-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-TTC34 Antibody (A19531-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279872026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10580-1-fam29a-haus6-primary-antibodies-wb-testing-1.jpgAnti-FAM29A/HAUS6 Antibody Picoband® Western blot analysis of FAM29A/HAUS6 using anti-FAM29A/HAUS6 antibody (A10580-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HEL whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FAM29A/HAUS6 antigen affinity purified polyclonal antibody (A10580-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for FAM29A/HAUS6 at approximately 109 kDa. The expected band size for FAM29A/HAUS6 is at 109 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10580-1-fam29a-haus6-primary-antibodies-if-testing-2.jpgAnti-FAM29A/HAUS6 Antibody Picoband® IF analysis of FAM29A/HAUS6 using anti-FAM29A/HAUS6 antibody (A10580-1) and anti-Beta Tubulin antibody (M01857-3). FAM29A/HAUS6 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-FAM29A/HAUS6 Antibody (A10580-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10580-1-fam29a-primary-antibodies-ip-testing-3.jpgAnti-FAM29A/HAUS6 Antibody Picoband® Immunoprecipitating FAM29A/HAUS6 in MCF-7 whole cell lysate. Western blot analysis of FAM29A/HAUS6 using anti-FAM29A/HAUS6 antibody (A10580-1); Lane 1: MCF-7 whole cell lysates (30ug); Lane 2: Rabbit control IgG instead of anti-FAM29A/HAUS6 antibody in MCF-7 whole cell lysate; Lane 3: anti-FAM29A/HAUS6 antibody (2μg) + MCF-7 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FAM29A/HAUS6 antigen affinity purified polyclonal antibody (A10580-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1196-200). A specific band was detected for FAM29A/HAUS6 at approximately 109 kDa. The expected band size for FAM29A/HAUS6 is at 109 kDa. https://www.bosterbio.com/catalog/product/view/id/1279882026-03-17T05:16:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05286-1-ctnnbl1-primary-antibodies-wb-testing-1.jpgAnti-CTNNBL1 Antibody Picoband® Western blot analysis of CTNNBL1 using anti-CTNNBL1 antibody (A05286-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTNNBL1 antigen affinity purified polyclonal antibody (A05286-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CTNNBL1 at approximately 65 kDa. The expected band size for CTNNBL1 is at 65 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05286-1-ctnnbl1-primary-antibodies-fcm-testing-2.jpgAnti-CTNNBL1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-CTNNBL1 antibody (A05286-1). Overlay histogram showing HEL cells stained with A05286-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CTNNBL1 Antibody (A05286-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279892026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06299-2-cyp2w1-primary-antibodies-wb-testing-1.jpgAnti-CYP2W1 Antibody Picoband® Western blot analysis of CYP2W1 using anti-CYP2W1 antibody (A06299-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYP2W1 antigen affinity purified polyclonal antibody (A06299-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CYP2W1 at approximately 54 kDa. The expected band size for CYP2W1 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06299-2-cyp2w1-primary-antibodies-ihc-testing-2_1.jpgAnti-CYP2W1 Antibody Picoband® IHC analysis of CYP2W1 using anti-CYP2W1 antibody (A06299-2). CYP2W1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CYP2W1 Antibody (A06299-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06299-2-cyp2w1-primary-antibodies-ihc-testing-3_1.jpgAnti-CYP2W1 Antibody Picoband® IHC analysis of CYP2W1 using anti-CYP2W1 antibody (A06299-2). CYP2W1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CYP2W1 Antibody (A06299-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06299-2-cyp2w1-primary-antibodies-ihc-testing-4_1.jpgAnti-CYP2W1 Antibody Picoband® IHC analysis of CYP2W1 using anti-CYP2W1 antibody (A06299-2). CYP2W1 was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CYP2W1 Antibody (A06299-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1279902026-03-25T05:24:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11105-1-nol9-primary-antibodies-wb-testing-1.jpgAnti-NOL9 Antibody Picoband® Western blot analysis of NOL9 using anti-NOL9 antibody (A11105-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human Hela whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NOL9 antigen affinity purified polyclonal antibody (A11105-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NOL9 at approximately 79 kDa. The expected band size for NOL9 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11105-1-nol9-primary-antibodies-if-testing-2.jpgAnti-NOL9 Antibody Picoband® IF analysis of NOL9 using anti-NOL9 antibody (A11105-1) and anti-Beta Tubulin antibody (M01857-3). NOL9 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NOL9 Antibody (A11105-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11105-1-nol9-primary-antibodies-fcm-testing-3.jpgAnti-NOL9 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-NOL9 antibody (A11105-1). Overlay histogram showing HepG2 cells stained with A11105-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NOL9 Antibody (A11105-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279912026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10975-1-ifi44l-primary-antibodies-wb-testing-1.jpgAnti-IFI44L Antibody Picoband® Western blot analysis of IFI44L using anti-IFI44L antibody (A10975-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human PC-3 whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: monkey COS-7 whole cell lysates, Lane 5: mouse NRK whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-IFI44L antigen affinity purified polyclonal antibody (A10975-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for IFI44L at approximately 51 kDa. The expected band size for IFI44L is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10975-1-ifi44l-primary-antibodies-ihc-testing-2.jpgAnti-IFI44L Antibody Picoband® IHC analysis of IFI44L using anti-IFI44L antibody (A10975-1). IFI44L was detected in a paraffin-embedded section of human non-small cell lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFI44L Antibody (A10975-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10975-1-ifi44l-primary-antibodies-ihc-testing-3.jpgAnti-IFI44L Antibody Picoband® IHC analysis of IFI44L using anti-IFI44L antibody (A10975-1). IFI44L was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-IFI44L Antibody (A10975-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10975-1-ifi44l-primary-antibodies-if-testing-4.jpgAnti-IFI44L Antibody Picoband® IF analysis of IFI44L using anti-IFI44L antibody (A10975-1). IFI44L was detected in an immunocytochemical section of SiHa cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-IFI44L Antibody (A10975-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10975-1-ifi44l-primary-antibodies-fcm-testing-5.jpgAnti-IFI44L Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-IFI44L antibody (A10975-1). Overlay histogram showing SiHa cells stained with A10975-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-IFI44L Antibody (A10975-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279922026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01737-2-cyp4f2-primary-antibodies-wb-testing-1.jpgAnti-CYP4F2 Antibody Picoband® Western blot analysis of CYP4F2 using anti-CYP4F2 antibody (A01737-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CYP4F2 antigen affinity purified polyclonal antibody (A01737-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CYP4F2 at approximately 50 kDa. The expected band size for CYP4F2 is at 60 kDa. https://www.bosterbio.com/catalog/product/view/id/1279932026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03815-1-hbz-primary-antibodies-wb-testing-1.jpgAnti-HBZ Antibody Picoband® Western blot analysis of HBZ using anti-HBZ antibody (A03815-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat bone tissue lysates, Lane 2: mouse bone tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-HBZ antigen affinity purified polyclonal antibody (A03815-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for HBZ at approximately 14 kDa. The expected band size for HBZ is at 16 kDa. https://www.bosterbio.com/catalog/product/view/id/1279942026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13315-1-glod4-primary-antibodies-wb-testing-1.jpgAnti-GLOD4 Antibody Picoband® Western blot analysis of GLOD4 using anti-GLOD4 antibody (A13315-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human U2OS whole cell lysates, Lane 4: human A431 whole cell lysates, Lane 5: rat stomach tissue lysates, Lane 6: rat liver tissue lysates, Lane 7: mouse stomach tissue lysates, Lane 8: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLOD4 antigen affinity purified polyclonal antibody (A13315-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLOD4 at approximately 35 kDa. The expected band size for GLOD4 is at 35 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13315-1-glod4-primary-antibodies-fcm-testing-2.jpgAnti-GLOD4 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-GLOD4 antibody (A13315-1). Overlay histogram showing HepG2 cells stained with A13315-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLOD4 Antibody (A13315-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279952026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00647-cacna1a-primary-antibodies-wb-testing-1.jpgAnti-CACNA1A Antibody Picoband® Western blot analysis of CACNA1A using anti-CACNA1A antibody (A00647). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CACNA1A antigen affinity purified polyclonal antibody (A00647) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CACNA1A at approximately 300 kDa. The expected band size for CACNA1A is at 282 kDa. https://www.bosterbio.com/catalog/product/view/id/1279962026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07686-4-card10-primary-antibodies-wb-testing-1.jpgAnti-CARD10 Antibody Picoband® Western blot analysis of CARD10 using anti-CARD10 antibody (A07686-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CARD10 antigen affinity purified polyclonal antibody (A07686-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CARD10 at approximately 116 kDa. The expected band size for CARD10 is at 116 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07686-4-card10-primary-antibodies-ihc-testing-2_1.jpgAnti-CARD10 Antibody Picoband® IHC analysis of CARD10 using anti-CARD10 antibody (A07686-4). CARD10 was detected in a paraffin-embedded section of human bladder cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CARD10 Antibody (A07686-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07686-4-card10-primary-antibodies-ihc-testing-3_1.jpgAnti-CARD10 Antibody Picoband® IHC analysis of CARD10 using anti-CARD10 antibody (A07686-4). CARD10 was detected in a paraffin-embedded section of mouse kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CARD10 Antibody (A07686-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07686-4-card10-primary-antibodies-ihc-testing-4_1.jpgAnti-CARD10 Antibody Picoband® IHC analysis of CARD10 using anti-CARD10 antibody (A07686-4). CARD10 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CARD10 Antibody (A07686-4) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07686-4-card10-primary-antibodies-fcm-testing-5_1.jpgAnti-CARD10 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-CARD10 antibody (A07686-4). Overlay histogram showing HepG2 cells stained with A07686-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CARD10 Antibody (A07686-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279972026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06600-1-cathepsin_f-ctsf-primary-antibodies-wb-testing-1.jpgAnti-Cathepsin F/CTSF Antibody Picoband® Western blot analysis of Cathepsin F/CTSF using anti-Cathepsin F/CTSF antibody (A06600-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human SiHa whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Cathepsin F/CTSF antigen affinity purified polyclonal antibody (A06600-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Cathepsin F/CTSF at approximately 53 kDa. The expected band size for Cathepsin F/CTSF is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06600-1-cathepsin_f-ctsf-primary-antibodies-ihc-testing-2.jpgAnti-Cathepsin F/CTSF Antibody Picoband® IHC analysis of Cathepsin F/CTSF using anti-Cathepsin F/CTSF antibody (A06600-1). Cathepsin F/CTSF was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Cathepsin F/CTSF Antibody (A06600-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06600-1-cathepsin_f-ctsf-primary-antibodies-ihc-testing-3.jpgAnti-Cathepsin F/CTSF Antibody Picoband® IHC analysis of Cathepsin F/CTSF using anti-Cathepsin F/CTSF antibody (A06600-1). Cathepsin F/CTSF was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-Cathepsin F/CTSF Antibody (A06600-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06600-1-cathepsin_f-ctsf-primary-antibodies-fcm-testing-4.jpgAnti-Cathepsin F/CTSF Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-Cathepsin F/CTSF antibody (A06600-1). Overlay histogram showing SiHa cells stained with A06600-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Cathepsin F/CTSF Antibody (A06600-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279982026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19277-glod5-primary-antibodies-wb-testing-1.jpgAnti-GLOD5 Antibody Picoband® Western blot analysis of GLOD5 using anti-GLOD5 antibody (A19277). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat small intestine tissue lysates, Lane 2: mouse small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GLOD5 antigen affinity purified polyclonal antibody (A19277) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for GLOD5 at approximately 16 kDa. The expected band size for GLOD5 is at 18 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19277-glod5-primary-antibodies-ihc-testing-2.jpgAnti-GLOD5 Antibody Picoband® IHC analysis of GLOD5 using anti-GLOD5 antibody (A19277). GLOD5 was detected in a paraffin-embedded section of human stomach tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLOD5 Antibody (A19277) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19277-glod5-primary-antibodies-ihc-testing-3.jpgAnti-GLOD5 Antibody Picoband® IHC analysis of GLOD5 using anti-GLOD5 antibody (A19277). GLOD5 was detected in a paraffin-embedded section of human stomach cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-GLOD5 Antibody (A19277) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a19277-glod5-primary-antibodies-fcm-testing-4.jpgAnti-GLOD5 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-GLOD5 antibody (A19277). Overlay histogram showing RT4 cells stained with A19277 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GLOD5 Antibody (A19277, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1279992026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09778-1-calpain_6-capn6-primary-antibodies-wb-testing-1.jpgAnti-Calpain 6/CAPN6 Antibody Picoband® Western blot analysis of Calpain 6/CAPN6 using anti-Calpain 6/CAPN6 antibody (A09778-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A549 whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: rat C6 whole cell lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Calpain 6/CAPN6 antigen affinity purified polyclonal antibody (A09778-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Calpain 6/CAPN6 at approximately 75 kDa. The expected band size for Calpain 6/CAPN6 is at 75 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09778-1-calpain_6-capn6-primary-antibodies-if-testing-2.jpgAnti-Calpain 6/CAPN6 Antibody Picoband® IF analysis of Calpain 6/CAPN6 using anti-Calpain 6/CAPN6 antibody (A09778-1). Calpain 6/CAPN6 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-Calpain 6/CAPN6 Antibody (A09778-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1280002026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05786-1-cdkn2aip-carf-primary-antibodies-wb-testing-1.jpgAnti-CDKN2AIP/CARF Antibody Picoband® Western blot analysis of CDKN2AIP/CARF using anti-CDKN2AIP/CARF antibody (A05786-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat lung tissue lysates, Lane 3: rat kidney tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse lung tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CDKN2AIP/CARF antigen affinity purified polyclonal antibody (A05786-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CDKN2AIP/CARF at approximately 75 kDa. The expected band size for CDKN2AIP/CARF is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05786-1-cdkn2aip-carf-primary-antibodies-fcm-testing-2.jpgAnti-CDKN2AIP/CARF Antibody Picoband® Flow Cytometry analysis of NIH/3T3 cells using anti-CDKN2AIP/CARF antibody (A05786-1). Overlay histogram showing NIH/3T3 cells stained with A05786-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CDKN2AIP/CARF Antibody (A05786-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280012026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08478-2-chp2-primary-antibodies-wb-testing-1.jpgAnti-CHP2 Antibody Picoband® Western blot analysis of CHP2 using anti-CHP2 antibody (A08478-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human PC-3 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CHP2 antigen affinity purified polyclonal antibody (A08478-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CHP2 at approximately 22 kDa. The expected band size for CHP2 is at 22 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08478-2-chp2-primary-antibodies-if-testing-2.jpgAnti-CHP2 Antibody Picoband® IF analysis of CHP2 using anti-CHP2 antibody (A08478-2) and anti-Beta Tubulin antibody (M01857-3). CHP2 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-CHP2 Antibody (A08478-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight®594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08478-2-chp2-primary-antibodies-fcm-testing-3.jpgAnti-CHP2 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-CHP2 antibody (A08478-2). Overlay histogram showing HepG2 cells stained with A08478-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CHP2 Antibody (A08478-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280022026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03954-4-cep55-primary-antibodies-wb-testing-1.jpgAnti-CEP55 Antibody Picoband® Western blot analysis of CEP55 using anti-CEP55 antibody (A03954-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human A431 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CEP55 antigen affinity purified polyclonal antibody (A03954-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CEP55 at approximately 54 kDa. The expected band size for CEP55 is at 54 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03954-4-cep55-primary-antibodies-fcm-testing-2.jpgAnti-CEP55 Antibody Picoband® Flow Cytometry analysis of A549 cells using anti-CEP55 antibody (A03954-4). Overlay histogram showing A549 cells stained with A03954-4 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CEP55 Antibody (A03954-4, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280032026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06361-4-cep135-primary-antibodies-wb-testing-1.jpgAnti-CEP135 Antibody Picoband® Western blot analysis of CEP135 using anti-CEP135 antibody (A06361-4). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human U-87MG whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CEP135 antigen affinity purified polyclonal antibody (A06361-4) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CEP135 at approximately 133 kDa. The expected band size for CEP135 is at 133 kDa. https://www.bosterbio.com/catalog/product/view/id/1280042026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01331-2-cit-primary-antibodies-wb-testing-1.jpgAnti-CIT Antibody Picoband® Western blot analysis of CIT using anti-CIT antibody (A01331-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CIT antigen affinity purified polyclonal antibody (A01331-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CIT at approximately 231 kDa. The expected band size for CIT is at 231 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01331-2-cit-primary-antibodies-fcm-testing-2.jpgAnti-CIT Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-CIT antibody (A01331-2). Overlay histogram showing SiHa cells stained with A01331-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CIT Antibody (A01331-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280052026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09747-1-b7h6-ncr3lg1-primary-antibodies-wb-testing-1.jpgAnti-B7H6/NCR3LG1 Antibody Picoband® Western blot analysis of B7H6/NCR3LG1 using anti-B7H6/NCR3LG1 antibody (A09747-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human HEL whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-B7H6/NCR3LG1 antigen affinity purified polyclonal antibody (A09747-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for B7H6/NCR3LG1 at approximately 90 kDa. The expected band size for B7H6/NCR3LG1 is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09747-1-b7h6-ncr3lg1-primary-antibodies-ihc-testing-2.jpgAnti-B7H6/NCR3LG1 Antibody Picoband® IHC analysis of B7H6/NCR3LG1 using anti-B7H6/NCR3LG1 antibody (A09747-1). B7H6/NCR3LG1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-B7H6/NCR3LG1 Antibody (A09747-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09747-1-b7h6-ncr3lg1-primary-antibodies-fcm-testing-3.jpgAnti-B7H6/NCR3LG1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-B7H6/NCR3LG1 antibody (A09747-1). Overlay histogram showing HepG2 cells stained with A09747-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-B7H6/NCR3LG1 Antibody (A09747-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280062026-03-17T05:16:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00391-3-marco-primary-antibodies-wb-testing-1.jpgAnti-MARCO Antibody Picoband® Western blot analysis of MARCO using anti-MARCO antibody (A00391-3). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human U2OS whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human A431 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MARCO antigen affinity purified polyclonal antibody (A00391-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for MARCO at approximately 53 kDa. The expected band size for MARCO is at 53 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00391-3-marco-primary-antibodies-fcm-testing-2.jpgAnti-MARCO Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-MARCO antibody (A00391-3). Overlay histogram showing THP-1 cells stained with A00391-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MARCO Antibody (A00391-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280072026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09341-1-nsl1-primary-antibodies-wb-testing-1.jpgAnti-NSL1 Antibody Picoband® Western blot analysis of NSL1 using anti-NSL1 antibody (A09341-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat thymus tissue lysates, Lane 2: rat RH-35 whole cell lysates, Lane 3: mouse thymus tissue lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NSL1 antigen affinity purified polyclonal antibody (A09341-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NSL1 at approximately 32 kDa. The expected band size for NSL1 is at 32 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09341-1-nsl1-primary-antibodies-fcm-testing-2.jpgAnti-NSL1 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-NSL1 antibody (A09341-1). Overlay histogram showing HepG2 cells stained with A09341-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NSL1 Antibody (A09341-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280082026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10663-1-nudt7-primary-antibodies-wb-testing-1.jpgAnti-NUDT7 Antibody Picoband® Western blot analysis of NUDT7 using anti-NUDT7 antibody (A10663-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human HepG2 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT7 antigen affinity purified polyclonal antibody (A10663-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for NUDT7 at approximately 27 kDa. The expected band size for NUDT7 is at 27 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10663-1-nudt7-primary-antibodies-ihc-testing-2.jpgAnti-NUDT7 Antibody Picoband® IHC analysis of NUDT7 using anti-NUDT7 antibody (A10663-1). NUDT7 was detected in a paraffin-embedded section of human liver tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT7 Antibody (A10663-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10663-1-nudt7-primary-antibodies-ihc-testing-3.jpgAnti-NUDT7 Antibody Picoband® IHC analysis of NUDT7 using anti-NUDT7 antibody (A10663-1). NUDT7 was detected in a paraffin-embedded section of human liver cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-NUDT7 Antibody (A10663-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10663-1-nudt7-primary-antibodies-fcm-testing-4.jpgAnti-NUDT7 Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-NUDT7 antibody (A10663-1). Overlay histogram showing THP-1 cells stained with A10663-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDT7 Antibody (A10663-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280092026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11219-2-rem2-primary-antibodies-wb-testing-1.jpgAnti-REM2 Antibody Picoband® Western blot analysis of REM2 using anti-REM2 antibody (A11219-2). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human SH-SY5Y whole cell lysates, Lane 3: human Hacat whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-REM2 antigen affinity purified polyclonal antibody (A11219-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for REM2 at approximately 37 kDa. The expected band size for REM2 is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11219-2-rem2-primary-antibodies-fcm-testing-2.jpgAnti-REM2 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-REM2 antibody (A11219-2). Overlay histogram showing Jurkat cells stained with A11219-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-REM2 Antibody (A11219-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280102026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10549-1-polr1a-primary-antibodies-wb-testing-1.jpgAnti-POLR1A Antibody Picoband® Western blot analysis of POLR1A using anti-POLR1A antibody (A10549-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human Caco-2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POLR1A antigen affinity purified polyclonal antibody (A10549-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POLR1A at approximately 195 kDa. The expected band size for POLR1A is at 195 kDa. https://www.bosterbio.com/catalog/product/view/id/1280112026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04295-1-pomt1-primary-antibodies-wb-testing-1.jpgAnti-POMT1 Antibody Picoband® Western blot analysis of POMT1 using anti-POMT1 antibody (A04295-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human MCF-7 whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POMT1 antigen affinity purified polyclonal antibody (A04295-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for POMT1 at approximately 75 kDa. The expected band size for POMT1 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04295-1-pomt1-primary-antibodies-fcm-testing-2.jpgAnti-POMT1 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-POMT1 antibody (A04295-1). Overlay histogram showing MCF-7 cells stained with A04295-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-POMT1 Antibody (A04295-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1280122026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03540-1-ctrc-primary-antibodies-wb-testing-1.jpgAnti-CTRC Antibody Picoband® Western blot analysis of CTRC using anti-CTRC antibody (A03540-1). Electrophoresis was performed on a 5-20% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human THP-1 whole cell lysates, Lane 3: rat pancreas tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTRC antigen affinity purified polyclonal antibody (A03540-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for CTRC at approximately 34 kDa. The expected band size for CTRC is at 29 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03540-1-ctrc-primary-antibodies-ihc-testing-3.jpgAnti-CTRC Antibody Picoband®IHC analysis of CTRC using anti-CTRC antibody (A03540-1). CTRC was detected in a paraffin-embedded section of human pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CTRC Antibody (A03540-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03540-1-ctrc-primary-antibodies-ihc-testing-2.jpgAnti-CTRC Antibody Picoband® IHC analysis of CTRC using anti-CTRC antibody (A03540-1). CTRC was detected in a paraffin-embedded section of rat pancreas tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-CTRC Antibody (A03540-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/all-recombinant-proteins/mouse-vegfr1-recombinant-protein-protp35969-1-boster.html2026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp35969-1_sds-page.jpg Mouse VEGFR1/Flt-1 Recombinant Protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stainhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp35969-1_biological_activity.jpg Mouse VEGFR1/Flt-1 Recombinant ProteinMouse VEGFR1/Flt-1 inhibit proliferation of the HUVEC human umbilical vein endothelial cells in the presence of Human VEGF165. The ED50 range ≤ 50 ng/ml. https://www.bosterbio.com/products/all-recombinant-proteins/human-flt3lg-recombinant-protein-protp49771-9-boster.html2026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49771-9-sds-page.jpgHuman Flt3 ligand/FLT3LG Recombinant protein3ug by SDS-PAGE under reducing condition and visualized by coomassie blue stain.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/p/r/protp49771-9-biological-activity_1.jpgHuman Flt3 ligand/FLT3LG Recombinant proteinHuman Flt3 ligand stimulates cell proliferation of the OCI-AML5 acute myeloid leukemia cells. The ED50 range ≤ 5 ng/ml. https://www.bosterbio.com/products/primary-antibodies/anti-drosophila-melanogaster-fruit-fly-unc13a-protein-antibody-dz41657-boster.html2026-03-10T04:38:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-drosophila-melanogaster-fruit-fly-brp-antibody-dz41659-boster.html2026-03-10T04:38:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-fundulus-heteroclitus-killifish-serine-threonine-protein-kinase-antibody-dz41662-boster.html2026-03-10T04:38:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-mus-musculus-mouse-grin2d-antibody-dz41652-boster.html2026-03-10T04:38:40+00:00daily0.9 https://www.bosterbio.com/products/primary-antibodies/anti-drosophila-melanogaster-fruit-fly-ctrip-antibody-dz41656-boster.html2026-03-10T04:38:40+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1280212026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0943_1.jpgMouse MPO/Myeloperoxidase PicoKine&reg Quick ELISA KitMouse MPO PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1280222026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0929_2.pngHuman IL-33 PicoKine&reg Quick ELISA KitHuman IL-33 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1280232026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-6-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (infliximab)The purity of Anti-TNFSF2/TNFa Reference Antibody (infliximab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-6-od450.jpgAnti-TNFSF2 / TNFa Reference Antibody (infliximab)Immobilized human TNFa https://www.bosterbio.com/catalog/product/view/id/1280242026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-7-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (golimumab)Anti-TNFSF2/TNFa Reference Antibody (golimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-7-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (golimumab)The purity of Anti-TNFSF2/TNFa Reference Antibody (golimumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280252026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-9-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (Afelimomab)Anti-TNFSF2/TNFa Reference Antibody (Afelimomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-9-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (Afelimomab)The purity of Anti-TNFSF2/TNFa Reference Antibody (Afelimomab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280262026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-10-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (licaminlimab)Anti-TNFSF2/TNFa Reference Antibody (licaminlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-10-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (licaminlimab)The purity of Anti-TNFSF2/TNFa Reference Antibody (licaminlimab)is more than 96.1% https://www.bosterbio.com/catalog/product/view/id/1280272026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-11-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (certolizumAb)Anti-TNFSF2/TNFa Reference Antibody (certolizumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-11-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (certolizumAb)The purity of Anti-TNFSF2/TNFa Reference Antibody (certolizumAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280282026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-12-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (CDP571)Anti-TNFSF2/TNFa Reference Antibody (CDP571) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-12-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (CDP571)The purity of Anti-TNFSF2/TNFa Reference Antibody (CDP571)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280292026-03-10T04:38:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-13-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (CMAB008)Anti-TNFSF2/TNFa Reference Antibody (CMAB008) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-13-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (CMAB008)The purity of Anti-TNFSF2/TNFa Reference Antibody (CMAB008)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280302026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-14-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (Epitomics patent anti-TNFalpha)Anti-TNFSF2/TNFa Reference Antibody (Epitomics patent anti-TNFalpha) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-14-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (Epitomics patent anti-TNFalpha)The purity of Anti-TNFSF2/TNFa Reference Antibody (Epitomics patent anti-TNFalpha)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280312026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-15-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (ESBA 105)Anti-TNFSF2/TNFa Reference Antibody (ESBA 105) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-15-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (ESBA 105)The purity of Anti-TNFSF2/TNFa Reference Antibody (ESBA 105)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280322026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-8-sds-page.jpgAnti-TNFSF2 / TNFa Reference Antibody (hMAK195)Anti-TNFSF2/TNFa Reference Antibody (hMAK195) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00002-8-sec-hplc.jpgAnti-TNFSF2 / TNFa Reference Antibody (hMAK195)The purity of Anti-TNFSF2/TNFa Reference Antibody (hMAK195)is more than 98.97% https://www.bosterbio.com/catalog/product/view/id/1280332026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-6-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (margetuximab)Anti-ERBB2/HER2/CD340 Reference Antibody (margetuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-6-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (margetuximab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (margetuximab)is more than 96.35% https://www.bosterbio.com/catalog/product/view/id/1280342026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-7-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (trastuzumab deruxtecan)Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab deruxtecan) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-7-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (trastuzumab deruxtecan)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab deruxtecan)is more than 93.54%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-7-od450.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (trastuzumab deruxtecan)Immobilized human HER2(23 652) His at 2 &mug/mL can bind Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab deruxtecan) https://www.bosterbio.com/catalog/product/view/id/1280352026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-8-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (pertuzumab)Anti-ERBB2/HER2/CD340 Reference Antibody (pertuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-8-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (pertuzumab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (pertuzumab)is more than 99.02%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-8-od450.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (pertuzumab)Immobilized human HER2(23 652) His at 2 &mug/mL can bind Anti-ERBB2/HER2/CD340 Reference Antibody (pertuzumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-8-facs.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (pertuzumab)BT474 cells were stained with Anti-ERBB2/HER2/CD340 Reference Antibody (pertuzumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-8-xenograft-nci-n87-cell-model.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (pertuzumab)Pertuzumab+trastuzumab inhibited the tumor growth of NCI-N87 on Balb/c nude mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1280362026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-10-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (trastuzumab-MMAE)Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-10-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (trastuzumab-MMAE)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab-MMAE)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-10-od450.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (trastuzumab-MMAE)Immobilized human HER2 His at 2 &mug/mL can bind Anti-ERBB2/HER2/CD340 Reference Antibody (trastuzumab-MMAE) https://www.bosterbio.com/catalog/product/view/id/1280372026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-11-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (disitamab)Anti-ERBB2/HER2/CD340 Reference Antibody (disitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-11-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (disitamab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (disitamab)is more than 98.73%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-11-od450.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (disitamab)Immobilized human ERBB2/HER2/CD340 https://www.bosterbio.com/catalog/product/view/id/1280382026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-12-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (zanidatamab)Anti-ERBB2/HER2/CD340 Reference Antibody (zanidatamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-12-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (zanidatamab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (zanidatamab)is more than 99.26% https://www.bosterbio.com/catalog/product/view/id/1280392026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-13-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Trastuzumab duocarmazine)Anti-ERBB2/HER2/CD340 Reference Antibody (Trastuzumab duocarmazine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-13-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Trastuzumab duocarmazine)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (Trastuzumab duocarmazine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280402026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-14-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (timigutuzumab)Anti-ERBB2/HER2/CD340 Reference Antibody (timigutuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-14-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (timigutuzumab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (timigutuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280412026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-15-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (disitamab vedotin)Anti-ERBB2/HER2/CD340 Reference Antibody (disitamab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-15-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (disitamab vedotin)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (disitamab vedotin)is more than 98.7% https://www.bosterbio.com/catalog/product/view/id/1280422026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-16-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (gancotamab)Anti-ERBB2/HER2/CD340 Reference Antibody (gancotamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-16-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (gancotamab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (gancotamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280432026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-17-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Anbenitamab)Anti-ERBB2/HER2/CD340 Reference Antibody (Anbenitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-17-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Anbenitamab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (Anbenitamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280442026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-18-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (BioMab patent anti-Her2)Anti-ERBB2/HER2/CD340 Reference Antibody (BioMab patent anti-Her2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-18-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (BioMab patent anti-Her2)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (BioMab patent anti-Her2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280452026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-19-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (coprelotamab)Anti-ERBB2/HER2/CD340 Reference Antibody (coprelotamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-19-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (coprelotamab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (coprelotamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280462026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-20-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Hersintuzumab)Anti-ERBB2/HER2/CD340 Reference Antibody (Hersintuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-20-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Hersintuzumab)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (Hersintuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280472026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-9-sds-page.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Trastuzumab emtansine)Anti-ERBB2/HER2/CD340 Reference Antibody (Trastuzumab emtansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00010-9-sec-hplc.jpgAnti-ERBB2 / HER2 / CD340 Reference Antibody (Trastuzumab emtansine)The purity of Anti-ERBB2/HER2/CD340 Reference Antibody (Trastuzumab emtansine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280482026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00017-sds-page.jpgAnti-TLR4 Reference Antibody(Paridiprubart)Anti-TLR4 Reference Antibody (Paridiprubart) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00017-sec-hplc.jpgAnti-TLR4 Reference Antibody(Paridiprubart)The purity of Anti-TLR4 Reference Antibody (Paridiprubart)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280492026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-5-sds-page.jpgAnti-TGFb1 Reference Antibody (fresolimumab)Anti-TGFb1 Reference Antibody (fresolimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-5-sec-hplc.jpgAnti-TGFb1 Reference Antibody (fresolimumab)The purity of Anti-TGFb1 Reference Antibody (fresolimumab)is more than 97.38%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-5-od450.jpgAnti-TGFb1 Reference Antibody (fresolimumab)Immobilized human Latent TGF beta 1/TGFB 1 https://www.bosterbio.com/catalog/product/view/id/1280502026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-6-sds-page.jpgAnti-TGFb1 Reference Antibody (SRK181)Anti-TGFb1 Reference Antibody (SRK181) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-6-sec-hplc.jpgAnti-TGFb1 Reference Antibody (SRK181)The purity of Anti-TGFb1 Reference Antibody (SRK181)is more than 97.59%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-6-od450.jpgAnti-TGFb1 Reference Antibody (SRK181)Immobilized human TGFb1 His at 2 &mug/mL can bind Anti-TGFb1 Reference Antibody (SRK181) https://www.bosterbio.com/catalog/product/view/id/1280512026-03-10T04:38:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-7-sds-page.jpgAnti-TGFb1 Reference Antibody (M7824)Anti-TGFb1 Reference Antibody (M7824) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90.7%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-7-sec-hplc.jpgAnti-TGFb1 Reference Antibody (M7824)The purity of Anti-TGFb1 Reference Antibody (M7824)is more than 96.19%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-7-od450.jpgAnti-TGFb1 Reference Antibody (M7824)Immobilized human PD L1 FC at 2 &mug/mL can bind Anti-TGFb1 Reference Antibody (M7824) https://www.bosterbio.com/catalog/product/view/id/1280522026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-8-sds-page.jpgAnti-TGFb1 Reference Antibody (Metelimumab)Anti-TGFb1 Reference Antibody (Metelimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-8-sec-hplc.jpgAnti-TGFb1 Reference Antibody (Metelimumab)The purity of Anti-TGFb1 Reference Antibody (Metelimumab)is more than 98.98% https://www.bosterbio.com/catalog/product/view/id/1280532026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-9-sds-page.jpgAnti-TGFb1 Reference Antibody (NIS793)Anti-TGFb1 Reference Antibody (NIS793) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-9-sec-hplc.jpgAnti-TGFb1 Reference Antibody (NIS793)The purity of Anti-TGFb1 Reference Antibody (NIS793)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280542026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-10-sds-page.jpgAnti-TGFb1 Reference Antibody (Genzyme patent anti-TGF-beta)Anti-TGFb1 Reference Antibody (Genzyme patent anti-TGF-beta) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00019-10-sec-hplc.jpgAnti-TGFb1 Reference Antibody (Genzyme patent anti-TGF-beta)The purity of Anti-TGFb1 Reference Antibody (Genzyme patent anti-TGF-beta)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280552026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-4-sds-page.jpgAnti-CTLA-4 / CD152 Reference Antibody (Antitope patent anti-CTLA4)Anti-CTLA-4/CD152 Reference Antibody (Antitope patent anti-CTLA4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-4-sec-hplc.jpgAnti-CTLA-4 / CD152 Reference Antibody (Antitope patent anti-CTLA4)The purity of Anti-CTLA-4/CD152 Reference Antibody (Antitope patent anti-CTLA4)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-4-od450.jpgAnti-CTLA-4 / CD152 Reference Antibody (Antitope patent anti-CTLA4)Immobilized human CTLA 4 His at 2 &mug/mL can bind Anti-CTLA-4/CD152 Reference Antibody (Antitope patent anti-CTLA4) https://www.bosterbio.com/catalog/product/view/id/1280562026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-9-sds-page.jpgAnti-CTLA-4 / CD152 Reference Antibody (nurulimab)Anti-CTLA-4/CD152 Reference Antibody (nurulimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-9-sec-hplc.jpgAnti-CTLA-4 / CD152 Reference Antibody (nurulimab)The purity of Anti-CTLA-4/CD152 Reference Antibody (nurulimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1280572026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-6-sds-page.jpgAnti-CTLA-4 / CD152 Reference Antibody (quavonlimab)Anti-CTLA-4/CD152 Reference Antibody (quavonlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-6-sec-hplc.jpgAnti-CTLA-4 / CD152 Reference Antibody (quavonlimab)The purity of Anti-CTLA-4/CD152 Reference Antibody (quavonlimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280582026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-7-sds-page.jpgAnti-CTLA-4 / CD152 Reference Antibody (ipilimumab)Anti-CTLA-4/CD152 Reference Antibody (ipilimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-7-sec-hplc.jpgAnti-CTLA-4 / CD152 Reference Antibody (ipilimumab)The purity of Anti-CTLA-4/CD152 Reference Antibody (ipilimumab)is more than 99.37%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-7-facs.jpgAnti-CTLA-4 / CD152 Reference Antibody (ipilimumab)Human CTLA-4 & Human PD-1 CHO-K cells were stained with Anti-CTLA-4/CD152 Reference Antibody (ipilimumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-7-syngenic-mc38-cell-model.jpgAnti-CTLA-4 / CD152 Reference Antibody (ipilimumab)Ipilimumab inhibited the tumor growth of MC38 on huCTLA-4 mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1280592026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-8-sds-page.jpgAnti-CTLA-4 / CD152 Reference Antibody (zalifrelimab)Anti-CTLA-4/CD152 Reference Antibody (zalifrelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-8-sec-hplc.jpgAnti-CTLA-4 / CD152 Reference Antibody (zalifrelimab)The purity of Anti-CTLA-4/CD152 Reference Antibody (zalifrelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280602026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-5-sds-page.jpgAnti-CTLA-4 / CD152 Reference Antibody (tremelimumab)Anti-CTLA-4/CD152 Reference Antibody (tremelimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-5-sec-hplc.jpgAnti-CTLA-4 / CD152 Reference Antibody (tremelimumab)The purity of Anti-CTLA-4/CD152 Reference Antibody (tremelimumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00020-5-od450.jpgAnti-CTLA-4 / CD152 Reference Antibody (tremelimumab)Immobilized human CTLA 4 His at 2 &mug/mL can bind Anti-CTLA-4/CD152 Reference Antibody (tremelimumab) https://www.bosterbio.com/catalog/product/view/id/1280612026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00021-2-sds-page.jpgAnti-IL-10 Reference Antibody (BT-063)Anti-IL-10 Reference Antibody (BT-063) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00021-2-sec-hplc.jpgAnti-IL-10 Reference Antibody (BT-063)The purity of Anti-IL-10 Reference Antibody (BT-063)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1280622026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-10-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (laprituximAb)Anti-ERBB1/EGFR/HER1 Reference Antibody (laprituximAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-10-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (laprituximAb)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (laprituximAb)is more than 98.97%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-10-od450.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (laprituximAb)Immobilized human EGFR His at 2 &mug/mL can bind Anti-ERBB1/EGFR/HER1 Reference Antibody (laprituximAb) https://www.bosterbio.com/catalog/product/view/id/1280632026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-11-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (panitumumab)Anti-ERBB1/EGFR/HER1 Reference Antibody (panitumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-11-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (panitumumab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (panitumumab)is more than 98.8%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-11-od450.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (panitumumab)Immobilized human EGFR His at 2 &mug/mL can bind Anti-ERBB1/EGFR/HER1 Reference Antibody (panitumumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-11-facs.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (panitumumab)NCI-H292 cells were stained with Anti-ERBB1/EGFR/HER1 Reference Antibody (panitumumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1280642026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-12-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Cetuximab-MMAE)Anti-ERBB1/EGFR/HER1 Reference Antibody (Cetuximab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-12-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Cetuximab-MMAE)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (Cetuximab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280652026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-13-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (pimurutamab)Anti-ERBB1/EGFR/HER1 Reference Antibody (pimurutamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-13-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (pimurutamab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (pimurutamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280662026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-14-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (demupitamab)Anti-ERBB1/EGFR/HER1 Reference Antibody (demupitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-14-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (demupitamab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (demupitamab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1280672026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-15-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Laprituximab emtansine)Anti-ERBB1/EGFR/HER1 Reference Antibody (Laprituximab emtansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-15-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Laprituximab emtansine)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (Laprituximab emtansine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280682026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-16-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (SerclutamAb)Anti-ERBB1/EGFR/HER1 Reference Antibody (SerclutamAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-16-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (SerclutamAb)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (SerclutamAb)is more than 94.3% https://www.bosterbio.com/catalog/product/view/id/1280692026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-17-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (losatuxizumAb)Anti-ERBB1/EGFR/HER1 Reference Antibody (losatuxizumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-17-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (losatuxizumAb)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (losatuxizumAb)is more than 99% https://www.bosterbio.com/catalog/product/view/id/1280702026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-18-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (depatuxizumab)Anti-ERBB1/EGFR/HER1 Reference Antibody (depatuxizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-18-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (depatuxizumab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (depatuxizumab)is more than 99.58%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-18-facs.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (depatuxizumab)Human EGFR CHO-K cells were stained with Anti-ERBB1/EGFR/HER1 Reference Antibody (depatuxizumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1280712026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-19-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (nimotuzumab)Anti-ERBB1/EGFR/HER1 Reference Antibody (nimotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-19-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (nimotuzumab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (nimotuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280722026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-20-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (tomuzotuximab)Anti-ERBB1/EGFR/HER1 Reference Antibody (tomuzotuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-20-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (tomuzotuximab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (tomuzotuximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280732026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-21-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (imgatuzumab)Anti-ERBB1/EGFR/HER1 Reference Antibody (imgatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-21-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (imgatuzumab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (imgatuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1280742026-03-10T04:38:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-22-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (modotuximab)Anti-ERBB1/EGFR/HER1 Reference Antibody (modotuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-22-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (modotuximab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (modotuximab)is more than 99.4% https://www.bosterbio.com/catalog/product/view/id/1280752026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-24-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (matuzumab)Anti-ERBB1/EGFR/HER1 Reference Antibody (matuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-24-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (matuzumab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (matuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280762026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-25-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Serclutamab talirine)Anti-ERBB1/EGFR/HER1 Reference Antibody (Serclutamab talirine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-25-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Serclutamab talirine)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (Serclutamab talirine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280772026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-26-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (7A7)Anti-ERBB1/EGFR/HER1 Reference Antibody (7A7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-26-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (7A7)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (7A7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280782026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-27-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (depatuxizumab-MMAF)Anti-ERBB1/EGFR/HER1 Reference Antibody (depatuxizumab-MMAF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-27-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (depatuxizumab-MMAF)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (depatuxizumab-MMAF)is more than 98.38% https://www.bosterbio.com/catalog/product/view/id/1280792026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-28-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Duke D2C7)Anti-ERBB1/EGFR/HER1 Reference Antibody (Duke D2C7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-28-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Duke D2C7)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (Duke D2C7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280802026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-29-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Regeneron patent anti-EGFR)Anti-ERBB1/EGFR/HER1 Reference Antibody (Regeneron patent anti-EGFR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-29-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Regeneron patent anti-EGFR)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (Regeneron patent anti-EGFR)is more than 99.32% https://www.bosterbio.com/catalog/product/view/id/1280812026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-23-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Shanghai Cancer Inst patent anti-EGFRvIII)Anti-ERBB1/EGFR/HER1 Reference Antibody (Shanghai Cancer Inst patent anti-EGFRvIII) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-23-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Shanghai Cancer Inst patent anti-EGFRvIII)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (Shanghai Cancer Inst patent anti-EGFRvIII)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280822026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-7-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (necitumumab)Anti-ERBB1/EGFR/HER1 Reference Antibody (necitumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-7-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (necitumumab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (necitumumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-7-od450.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (necitumumab)Immobilized human EGFR His at 2 &mug/mL can bind Anti-ERBB1/EGFR/HER1 Reference Antibody (necitumumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-7-facs.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (necitumumab)Human EGFR CHO-K cells were stained with Anti-ERBB1/EGFR/HER1 Reference Antibody (necitumumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1280832026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-8-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (zalutumumab)Anti-ERBB1/EGFR/HER1 Reference Antibody (zalutumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-8-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (zalutumumab)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (zalutumumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-8-od450.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (zalutumumab)Immobilized human EGFR His at 2 &mug/mL can bind Anti-ERBB1/EGFR/HER1 Reference Antibody (zalutumumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-8-facs.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (zalutumumab)Human EGFR CHO-K cells were stained with Anti-ERBB1/EGFR/HER1 Reference Antibody (zalutumumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1280842026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-9-sds-page.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Chinese Mil.Med.Sci. patent anti-EGFR)Anti-ERBB1/EGFR/HER1 Reference Antibody (Chinese Mil.Med.Sci. patent anti-EGFR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00023-9-sec-hplc.jpgAnti-ERBB1 / EGFR / HER1 Reference Antibody (Chinese Mil.Med.Sci. patent anti-EGFR)The purity of Anti-ERBB1/EGFR/HER1 Reference Antibody (Chinese Mil.Med.Sci. patent anti-EGFR)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1280852026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00031-1-sds-page.jpgAnti-CXCR4 / CD184 Reference Antibody (ulocuplumab)Anti-CXCR4/CD184 Reference Antibody (ulocuplumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00031-1-sec-hplc.jpgAnti-CXCR4 / CD184 Reference Antibody (ulocuplumab)The purity of Anti-CXCR4/CD184 Reference Antibody (ulocuplumab)is more than 99.48%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00031-1-facs.jpgAnti-CXCR4 / CD184 Reference Antibody (ulocuplumab)Human CXCR4 Romas cells were stained with Anti-CXCR4/CD184 Reference Antibody (ulocuplumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1280862026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00031-2-sds-page.jpgAnti-CXCR4 / CD184 Reference Antibody (Dana-Farber patent anti-CXCR4)Anti-CXCR4/CD184 Reference Antibody (Dana-Farber patent anti-CXCR4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00031-2-sec-hplc.jpgAnti-CXCR4 / CD184 Reference Antibody (Dana-Farber patent anti-CXCR4)The purity of Anti-CXCR4/CD184 Reference Antibody (Dana-Farber patent anti-CXCR4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280872026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00031-3-sds-page.jpgAnti-CXCR4/CD184 Reference Antibody (ulocuplumab-MMAE)Anti-CXCR4/CD184 Reference Antibody (ulocuplumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00031-3-sec-hplc.jpgAnti-CXCR4/CD184 Reference Antibody (ulocuplumab-MMAE)The purity of Anti-CXCR4/CD184 Reference Antibody (ulocuplumab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280882026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00033-2-sds-page.jpgAnti-NOTCH1 Reference Antibody (brontictuzumab)Anti-NOTCH1 Reference Antibody (brontictuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00033-2-sec-hplc.jpgAnti-NOTCH1 Reference Antibody (brontictuzumab)The purity of Anti-NOTCH1 Reference Antibody (brontictuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280892026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00033-3-sds-page.jpgAnti-NOTCH1 Reference Antibody (Pfizer patent anti-Notch1)Anti-NOTCH1 Reference Antibody (Pfizer patent anti-Notch1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00033-3-sec-hplc.jpgAnti-NOTCH1 Reference Antibody (Pfizer patent anti-Notch1)The purity of Anti-NOTCH1 Reference Antibody (Pfizer patent anti-Notch1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280902026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-3-sds-page.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)Anti-VEGF Reference Antibody (BioMab patent anti-VEGF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-3-sec-hplc.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)The purity of Anti-VEGF Reference Antibody (BioMab patent anti-VEGF)is more than 97.8%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-3-od450.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)Immobilized human VEGF165 His at 2 &mug/mL can bind Anti-VEGF Reference Antibody (BioMab patent anti-VEGF)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-3-xenograft-colo205-cell-model.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)Bevacizumab inhibited the tumor growth of COLO205 on balb/c nude mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1280912026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-4-sds-page.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)Anti-VEGF Reference Antibody (BioMab patent anti-VEGF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-4-sec-hplc.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)The purity of Anti-VEGF Reference Antibody (BioMab patent anti-VEGF)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1280922026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-5-sds-page.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)Anti-VEGF Reference Antibody (BioMab patent anti-VEGF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-5-sec-hplc.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)The purity of Anti-VEGF Reference Antibody (BioMab patent anti-VEGF)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280932026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-6-sds-page.jpgAnti-VEGF Reference Antibody (BioMab patent anti-VEGF)Anti-VEGF Reference Antibody (BioMab patent anti-VEGF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90% https://www.bosterbio.com/catalog/product/view/id/1280942026-03-10T04:38:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-7-sds-page.jpgAnti-VEGF Reference Antibody (Domantis patent anti-VEGF)Anti-VEGF Reference Antibody (Domantis patent anti-VEGF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00045-7-sec-hplc.jpgAnti-VEGF Reference Antibody (Domantis patent anti-VEGF)The purity of Anti-VEGF Reference Antibody (Domantis patent anti-VEGF)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280952026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00052-6-sds-page.jpgAnti-CD44v6 Reference Antibody (bivatuzumab)Anti-CD44v6 Reference Antibody (bivatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00052-6-sec-hplc.jpgAnti-CD44v6 Reference Antibody (bivatuzumab)The purity of Anti-CD44v6 Reference Antibody (bivatuzumab)is more than 98.38% https://www.bosterbio.com/catalog/product/view/id/1280962026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00053-1-sds-page.jpgAnti-CXCL12 / SDF1a Reference Antibody (Genentech anti-CXCL12)Anti-CXCL12/SDF1a Reference Antibody (Genentech anti-CXCL12) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00053-1-sec-hplc.jpgAnti-CXCL12 / SDF1a Reference Antibody (Genentech anti-CXCL12)The purity of Anti-CXCL12/SDF1a Reference Antibody (Genentech anti-CXCL12)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280972026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00056-2-sds-page.jpgAnti-CCL2 / MCP1 Reference Antibody (carlumab)Anti-CCL2/MCP1 Reference Antibody (carlumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00056-2-sec-hplc.jpgAnti-CCL2 / MCP1 Reference Antibody (carlumab)The purity of Anti-CCL2/MCP1 Reference Antibody (carlumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00056-2-od450.jpgAnti-CCL2 / MCP1 Reference Antibody (carlumab)Immobilized human MCP1 His at 2 &mug/mL can bind Anti-CCL2/MCP1 Reference Antibody (carlumab) https://www.bosterbio.com/catalog/product/view/id/1280982026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00060-sds-page.jpgAnti-Polyubiquitin Reference Antibody (Genentech patent anti-Polyubiquitin)Anti-Polyubiquitin Reference Antibody (Genentech patent anti-Polyubiquitin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00060-sec-hplc.jpgAnti-Polyubiquitin Reference Antibody (Genentech patent anti-Polyubiquitin)The purity of Anti-Polyubiquitin Reference Antibody (Genentech patent anti-Polyubiquitin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1280992026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00061-1-sds-page.jpgAnti-CCR5 / CD195 Reference Antibody (leronlimab)Anti-CCR5/CD195 Reference Antibody (leronlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00061-1-sec-hplc.jpgAnti-CCR5 / CD195 Reference Antibody (leronlimab)The purity of Anti-CCR5/CD195 Reference Antibody (leronlimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00061-1-facs.jpgAnti-CCR5 / CD195 Reference Antibody (leronlimab)Human CCR5 His EGFP HEK293 cells were stained with Anti-CCR5/CD195 Reference Antibody (leronlimab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1281002026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00062-4-sds-page.jpgAnti-Haptoglobin Reference Antibody (KHK patent anti-Haptoglobin)Anti-Haptoglobin Reference Antibody (KHK patent anti-Haptoglobin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00062-4-sec-hplc.jpgAnti-Haptoglobin Reference Antibody (KHK patent anti-Haptoglobin)The purity of Anti-Haptoglobin Reference Antibody (KHK patent anti-Haptoglobin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281012026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-6-sds-page.jpgAnti-CDH1 / E-cadherin / CD324 Reference Antibody (Stem Centrx patent anti-Cadherin-1)Anti-CDH1/E-cadherin/CD324 Reference Antibody (Stem Centrx patent anti-Cadherin-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-6-sec-hplc.jpgAnti-CDH1 / E-cadherin / CD324 Reference Antibody (Stem Centrx patent anti-Cadherin-1)The purity of Anti-CDH1/E-cadherin/CD324 Reference Antibody (Stem Centrx patent anti-Cadherin-1)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00063-6-od450.jpgAnti-CDH1 / E-cadherin / CD324 Reference Antibody (Stem Centrx patent anti-Cadherin-1)Immobilized human CDH1 His at 2 &mug/mL can bind Anti-CDH1/E-cadherin/CD324 Reference Antibody (Stem Centrx patent anti-Cadherin-1) https://www.bosterbio.com/catalog/product/view/id/1281022026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00065-3-sds-page.jpgAnti-CD28 Reference Antibody (Theralizumab)Anti-CD28 Reference Antibody (Theralizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00065-3-sec-hplc.jpgAnti-CD28 Reference Antibody (Theralizumab)The purity of Anti-CD28 Reference Antibody (Theralizumab)is more than 98.72% https://www.bosterbio.com/catalog/product/view/id/1281032026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00065-4-sds-page.jpgAnti-CD28 Reference Antibody (FR104)Anti-CD28 Reference Antibody (FR104) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00065-4-sec-hplc.jpgAnti-CD28 Reference Antibody (FR104)The purity of Anti-CD28 Reference Antibody (FR104)is more than 98.98% https://www.bosterbio.com/catalog/product/view/id/1281042026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00065-5-sds-page.jpgAnti-CD28 Reference Antibody (lulizumab)Anti-CD28 Reference Antibody (lulizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00065-5-sec-hplc.jpgAnti-CD28 Reference Antibody (lulizumab)The purity of Anti-CD28 Reference Antibody (lulizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1281052026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-3-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (Teneliximab)Anti-TNFRSF5/CD40 Reference Anticody (Teneliximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-3-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (Teneliximab)The purity of Anti-TNFRSF5/CD40 Reference Anticody (Teneliximab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-3-od450.jpgAnti-TNFRSF5 / CD40 Reference Antibody (Teneliximab)Immobilized Cynomolgus CD40/TNFRSF5 Protein https://www.bosterbio.com/catalog/product/view/id/1281062026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-13-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (selicrelumab)Anti-TNFRSF5/CD40 Reference Antibody (selicrelumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-13-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (selicrelumab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (selicrelumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-13-od450.jpgAnti-TNFRSF5 / CD40 Reference Antibody (selicrelumab)Immobilized human CD40 His at 2 &mug/mL can bind Anti-TNFRSF5/CD40 Reference Antibody (selicrelumab) https://www.bosterbio.com/catalog/product/view/id/1281072026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-14-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (sotigalimab)Anti-TNFRSF5/CD40 Reference Antibody (sotigalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-14-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (sotigalimab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (sotigalimab)is more than 98.9% https://www.bosterbio.com/catalog/product/view/id/1281082026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-6-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (Cifurtilimab)Anti-TNFRSF5/CD40 Reference Antibody (Cifurtilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-6-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (Cifurtilimab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (Cifurtilimab)is more than 97.87% https://www.bosterbio.com/catalog/product/view/id/1281092026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-7-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (ravagalimab)Anti-TNFRSF5/CD40 Reference Antibody (ravagalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-7-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (ravagalimab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (ravagalimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281102026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-8-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (lucatumumab)Anti-TNFRSF5/CD40 Reference Antibody (lucatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-8-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (lucatumumab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (lucatumumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281112026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-9-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (giloralimab)Anti-TNFRSF5/CD40 Reference Antibody (giloralimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-9-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (giloralimab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (giloralimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281122026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-10-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (iscalimab)Anti-TNFRSF5/CD40 Reference Antibody (iscalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-10-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (iscalimab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (iscalimab)is more than 99.15% https://www.bosterbio.com/catalog/product/view/id/1281132026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-11-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (mitazalimab)Anti-TNFRSF5/CD40 Reference Antibody (mitazalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-11-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (mitazalimab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (mitazalimab)is more than 98.06% https://www.bosterbio.com/catalog/product/view/id/1281142026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-12-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (Emory U. anti-CD40)Anti-TNFRSF5/CD40 Reference Antibody (Emory U. anti-CD40) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-12-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (Emory U. anti-CD40)The purity of Anti-TNFRSF5/CD40 Reference Antibody (Emory U. anti-CD40)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281152026-03-10T04:38:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-4-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (dacetuzumab)Anti-TNFRSF5/CD40 Reference Antibody (dacetuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-4-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (dacetuzumab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (dacetuzumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-4-od450.jpgAnti-TNFRSF5 / CD40 Reference Antibody (dacetuzumab)Immobilized human TNFRSF5/CD40 His at 2 &mug/mL can bind Anti-TNFRSF5/CD40 Reference Antibody (dacetuzumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-4-facs.jpgAnti-TNFRSF5 / CD40 Reference Antibody (dacetuzumab)Human CD40 CHO cells were stained with Anti-TNFRSF5/CD40 Reference Antibody (dacetuzumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1281162026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-5-sds-page.jpgAnti-TNFRSF5 / CD40 Reference Antibody (bleselumab)Anti-TNFRSF5/CD40 Reference Antibody (bleselumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-5-sec-hplc.jpgAnti-TNFRSF5 / CD40 Reference Antibody (bleselumab)The purity of Anti-TNFRSF5/CD40 Reference Antibody (bleselumab)is more than 99.21%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-5-od450.jpgAnti-TNFRSF5 / CD40 Reference Antibody (bleselumab)Immobilized human TNFRSF5/CD40 His at 2 &mug/mL can bind Anti-TNFRSF5/CD40 Reference Antibody (bleselumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-5-facs.jpgAnti-TNFRSF5 / CD40 Reference Antibody (bleselumab)Human CD40 CHO cells were stained with Anti-TNFRSF5/CD40 Reference Antibody (bleselumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00068-5-facs-1.jpgAnti-TNFRSF5 / CD40 Reference Antibody (bleselumab)Anti-TNFRSF5/CD40 Reference Antibody (bleselumab) FACS Blocking was evaluated using CCRF-CEM. The IC50 was approximately 1.359 ug/mL. https://www.bosterbio.com/catalog/product/view/id/1281172026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-3-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (cixutumumab)Anti-IGF1R/CD221 Reference Antibody (cixutumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-3-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (cixutumumab)The purity of Anti-IGF1R/CD221 Reference Antibody (cixutumumab)is more than 99.63% https://www.bosterbio.com/catalog/product/view/id/1281182026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-4-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (teprotumumab)Anti-IGF1R/CD221 Reference Antibody (teprotumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-4-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (teprotumumab)The purity of Anti-IGF1R/CD221 Reference Antibody (teprotumumab)is more than 96.97%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-4-od450.jpgAnti-IGF1R / CD221 Reference Antibody (teprotumumab)Immobilized human IGF1R His at 2 &mug/mL can bind Anti-IGF1R/CD221 Reference Antibody (teprotumumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-4-facs.jpgAnti-IGF1R / CD221 Reference Antibody (teprotumumab)Human IGF1R CHO-K1 cells were stained with Anti-IGF1R/CD221 Reference Antibody (teprotumumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1281192026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-5-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (lonigutamAb)Anti-IGF1R/CD221 Reference Antibody (lonigutamAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-5-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (lonigutamAb)The purity of Anti-IGF1R/CD221 Reference Antibody (lonigutamAb)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-5-od450.jpgAnti-IGF1R / CD221 Reference Antibody (lonigutamAb)Immobilized human IGF1R His at 2 &mug/mL can bind Anti-IGF1R/CD221 Reference Antibody (lonigutamAb) https://www.bosterbio.com/catalog/product/view/id/1281202026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-6-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (Lonigutamab-MMAE)Anti-IGF1R/CD221 Reference Antibody (Lonigutamab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-6-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (Lonigutamab-MMAE)The purity of Anti-IGF1R/CD221 Reference Antibody (Lonigutamab-MMAE)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1281212026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-7-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (robatumumab)Anti-IGF1R/CD221 Reference Antibody (robatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-7-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (robatumumab)The purity of Anti-IGF1R/CD221 Reference Antibody (robatumumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281222026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-8-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (ganitumab)Anti-IGF1R/CD221 Reference Antibody (ganitumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-8-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (ganitumab)The purity of Anti-IGF1R/CD221 Reference Antibody (ganitumab)is more than 100.00 % https://www.bosterbio.com/catalog/product/view/id/1281232026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-9-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (figitumumab)Anti-IGF1R/CD221 Reference Antibody (figitumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-9-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (figitumumab)The purity of Anti-IGF1R/CD221 Reference Antibody (figitumumab)is more than 99.24% https://www.bosterbio.com/catalog/product/view/id/1281242026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-10-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (dalotuzumab)Anti-IGF1R/CD221 Reference Antibody (dalotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-10-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (dalotuzumab)The purity of Anti-IGF1R/CD221 Reference Antibody (dalotuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281252026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-11-sds-page.jpgAnti-IGF1R / CD221 Reference Antibody (Immunomedics patent anti-IGF-1R)Anti-IGF1R/CD221 Reference Antibody (Immunomedics patent anti-IGF-1R) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00070-11-sec-hplc.jpgAnti-IGF1R / CD221 Reference Antibody (Immunomedics patent anti-IGF-1R)The purity of Anti-IGF1R/CD221 Reference Antibody (Immunomedics patent anti-IGF-1R)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281262026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-2-sds-page.jpgAnti-IL-13 Reference Antibody (tralokinumab)Anti-IL-13 Reference Antibody (tralokinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-2-sec-hplc.jpgAnti-IL-13 Reference Antibody (tralokinumab)The purity of Anti-IL-13 Reference Antibody (tralokinumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1281272026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-3-sds-page.jpgAnti-IL-13 Reference Antibody (lebrikizumab)Anti-IL-13 Reference Antibody (lebrikizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-3-sec-hplc.jpgAnti-IL-13 Reference Antibody (lebrikizumab)The purity of Anti-IL-13 Reference Antibody (lebrikizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281282026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-4-sds-page.jpgAnti-IL-13 Reference Antibody (anrukinzumab)Anti-IL-13 Reference Antibody (anrukinzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-4-sec-hplc.jpgAnti-IL-13 Reference Antibody (anrukinzumab)The purity of Anti-IL-13 Reference Antibody (anrukinzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281292026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-5-sds-page.jpgAnti-IL-13 Reference Antibody (IMA-026)Anti-IL-13 Reference Antibody (IMA-026) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-5-sec-hplc.jpgAnti-IL-13 Reference Antibody (IMA-026)The purity of Anti-IL-13 Reference Antibody (IMA-026)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281302026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-6-sds-page.jpgAnti-IL-13 Reference Antibody (GSK 679586)Anti-IL-13 Reference Antibody (GSK 679586) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-6-sec-hplc.jpgAnti-IL-13 Reference Antibody (GSK 679586)The purity of Anti-IL-13 Reference Antibody (GSK 679586)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281312026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-7-sds-page.jpgAnti-IL-13 Reference Antibody (abrezekimab)Anti-IL-13 Reference Antibody (abrezekimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-7-sec-hplc.jpgAnti-IL-13 Reference Antibody (abrezekimab)The purity of Anti-IL-13 Reference Antibody (abrezekimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281322026-03-10T04:38:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-8-sds-page.jpgAnti-IL-13 Reference Antibody (cendakimab)Anti-IL-13 Reference Antibody (cendakimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-8-sec-hplc.jpgAnti-IL-13 Reference Antibody (cendakimab)The purity of Anti-IL-13 Reference Antibody (cendakimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281332026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-9-sds-page.jpgAnti-IL-13 Reference Antibody (dectrekumab)Anti-IL-13 Reference Antibody (dectrekumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-9-sec-hplc.jpgAnti-IL-13 Reference Antibody (dectrekumab)The purity of Anti-IL-13 Reference Antibody (dectrekumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281342026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-10-sds-page.jpgAnti-IL-13 Reference Antibody (CNTO 607)Anti-IL-13 Reference Antibody (CNTO 607) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-10-sec-hplc.jpgAnti-IL-13 Reference Antibody (CNTO 607)The purity of Anti-IL-13 Reference Antibody (CNTO 607)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281352026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-11-sds-page.jpgAnti-IL-13 Reference Antibody (H2L6)Anti-IL-13 Reference Antibody (H2L6) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-11-sec-hplc.jpgAnti-IL-13 Reference Antibody (H2L6)The purity of Anti-IL-13 Reference Antibody (H2L6)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281362026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-12-sds-page.jpgAnti-IL-13 Reference Antibody (M1295)Anti-IL-13 Reference Antibody (M1295) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00077-12-sec-hplc.jpgAnti-IL-13 Reference Antibody (M1295)The purity of Anti-IL-13 Reference Antibody (M1295)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281372026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-10-sds-page.jpgAnti-Amyloid Beta Reference Antibody (GSK 933776)Anti-Amyloid Beta Reference Antibody (GSK 933776) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-10-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (GSK 933776)The purity of Anti-Amyloid Beta Reference Antibody (GSK 933776)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281382026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-11-sds-page.jpgAnti-Amyloid Beta Reference Antibody (bapineuzumab)Anti-Amyloid Beta Reference Antibody (bapineuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-11-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (bapineuzumab)The purity of Anti-Amyloid Beta Reference Antibody (bapineuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281392026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-12-sds-page.jpgAnti-Amyloid Beta Reference Antibody (Amgen patent anti-beta amyloid)Anti-Amyloid Beta Reference Antibody (Amgen patent anti-beta amyloid) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-12-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (Amgen patent anti-beta amyloid)The purity of Anti-Amyloid Beta Reference Antibody (Amgen patent anti-beta amyloid)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281402026-03-10T04:38:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-13-sds-page.jpgAnti-Amyloid Beta Reference Antibody (CNTO 2125)Anti-Amyloid Beta Reference Antibody (CNTO 2125) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-13-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (CNTO 2125)The purity of Anti-Amyloid Beta Reference Antibody (CNTO 2125)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281412026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-14-sds-page.jpgAnti-Amyloid Beta Reference Antibody (CSIRO anti-amyloid Beta scFv)Anti-Amyloid Beta Reference Antibody (CSIRO anti-amyloid Beta scFv) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-14-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (CSIRO anti-amyloid Beta scFv)The purity of Anti-Amyloid Beta Reference Antibody (CSIRO anti-amyloid Beta scFv)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281422026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-15-sds-page.jpgAnti-Amyloid Beta Reference Antibody (DLX212)Anti-Amyloid Beta Reference Antibody (DLX212) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-15-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (DLX212)The purity of Anti-Amyloid Beta Reference Antibody (DLX212)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281432026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-16-sds-page.jpgAnti-Amyloid Beta Reference Antibody (Georgetown U. patent anti-Amyloid Beta)Anti-Amyloid Beta Reference Antibody (Georgetown U. patent anti-Amyloid Beta) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-16-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (Georgetown U. patent anti-Amyloid Beta)The purity of Anti-Amyloid Beta Reference Antibody (Georgetown U. patent anti-Amyloid Beta)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281442026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-17-sds-page.jpgAnti-Amyloid Beta Reference Antibody (Kumamoto U. patent anti-Amyloid Beta)Anti-Amyloid Beta Reference Antibody (Kumamoto U. patent anti-Amyloid Beta) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-17-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (Kumamoto U. patent anti-Amyloid Beta)The purity of Anti-Amyloid Beta Reference Antibody (Kumamoto U. patent anti-Amyloid Beta)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281452026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-18-sds-page.jpgAnti-Amyloid Beta Reference Antibody (Merck anti-Amyloid beta 19.3)Anti-Amyloid Beta Reference Antibody (Merck anti-Amyloid beta 19.3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-18-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (Merck anti-Amyloid beta 19.3)The purity of Anti-Amyloid Beta Reference Antibody (Merck anti-Amyloid beta 19.3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281462026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-19-sds-page.jpgAnti-Amyloid Beta Reference Antibody (Merck patent anti-Amyloid Beta)Anti-Amyloid Beta Reference Antibody (Merck patent anti-Amyloid Beta) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-19-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (Merck patent anti-Amyloid Beta)The purity of Anti-Amyloid Beta Reference Antibody (Merck patent anti-Amyloid Beta)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281472026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-20-sds-page.jpgAnti-Amyloid Beta Reference Antibody (Rockefeller U. patent anti-Amyloid Beta)Anti-Amyloid Beta Reference Antibody (Rockefeller U. patent anti-Amyloid Beta) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-20-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (Rockefeller U. patent anti-Amyloid Beta)The purity of Anti-Amyloid Beta Reference Antibody (Rockefeller U. patent anti-Amyloid Beta)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281482026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-21-sds-page.jpgAnti-Amyloid Beta Reference Antibody (U.Illinois scFv59)Anti-Amyloid Beta Reference Antibody (U.Illinois scFv59) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-21-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (U.Illinois scFv59)The purity of Anti-Amyloid Beta Reference Antibody (U.Illinois scFv59)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281492026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-22-sds-page.jpgAnti-Amyloid Beta Reference Antibody (U.Zurich patent anti-Amyloid Beta)Anti-Amyloid Beta Reference Antibody (U.Zurich patent anti-Amyloid Beta) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-22-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (U.Zurich patent anti-Amyloid Beta)The purity of Anti-Amyloid Beta Reference Antibody (U.Zurich patent anti-Amyloid Beta)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281502026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-3-sds-page.jpgAnti-Amyloid Beta Reference Antibody (gantenerumab)Anti-Amyloid Beta Reference Antibody (gantenerumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-3-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (gantenerumab)The purity of Anti-Amyloid Beta Reference Antibody (gantenerumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-3-od450.jpgAnti-Amyloid Beta Reference Antibody (gantenerumab)Immobilized Abeta40 at 8 &mug/mL can bind Anti-Amyloid Beta Reference Antibody (gantenerumab) https://www.bosterbio.com/catalog/product/view/id/1281512026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-4-sds-page.jpgAnti-Amyloid Beta Reference Antibody (lecanemab)Anti-Amyloid Beta Reference Antibody (lecanemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-4-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (lecanemab)The purity of Anti-Amyloid Beta Reference Antibody (lecanemab)is more than 99.7%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-4-od450.jpgAnti-Amyloid Beta Reference Antibody (lecanemab)Immobilized Abeta42/Abeta40 at 2 &mug/mL can bind Anti-Amyloid Beta Reference Antibody (lecanemab) https://www.bosterbio.com/catalog/product/view/id/1281522026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-5-sds-page.jpgAnti-Amyloid Beta Reference Antibody (donanemab)Anti-Amyloid Beta Reference Antibody (donanemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-5-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (donanemab)The purity of Anti-Amyloid Beta Reference Antibody (donanemab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1281532026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-7-sds-page.jpgAnti-Amyloid Beta Reference Antibody (ponezumab)Anti-Amyloid Beta Reference Antibody (ponezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-7-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (ponezumab)The purity of Anti-Amyloid Beta Reference Antibody (ponezumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281542026-03-10T04:38:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-8-sds-page.jpgAnti-Amyloid Beta Reference Antibody (crenezumab)Anti-Amyloid Beta Reference Antibody (crenezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-8-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (crenezumab)The purity of Anti-Amyloid Beta Reference Antibody (crenezumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281552026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-6-sds-page.jpgAnti-Amyloid Beta Reference Antibody (solanezumab)Anti-Amyloid Beta Reference Antibody (solanezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00081-6-sec-hplc.jpgAnti-Amyloid Beta Reference Antibody (solanezumab)The purity of Anti-Amyloid Beta Reference Antibody (solanezumab)is more than 96.84% https://www.bosterbio.com/catalog/product/view/id/1281562026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-1-sds-page.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (cabiralizumab)Anti-CSF1R/M-CSFR/CD115 Reference Antibody (cabiralizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-1-sec-hplc.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (cabiralizumab)The purity of Anti-CSF1R/M-CSFR/CD115 Reference Antibody (cabiralizumab)is more than 99.14%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-1-od450.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (cabiralizumab)Immobilized human CSF1R/M CSFR https://www.bosterbio.com/catalog/product/view/id/1281572026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-2-sds-page.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (axatilimab)Anti-CSF1R/M-CSFR/CD115 Reference Antibody (axatilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-2-sec-hplc.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (axatilimab)The purity of Anti-CSF1R/M-CSFR/CD115 Reference Antibody (axatilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281582026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-3-sds-page.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (emactuzumab)Anti-CSF1R/M-CSFR/CD115 Reference Antibody (emactuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-3-sec-hplc.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (emactuzumab)The purity of Anti-CSF1R/M-CSFR/CD115 Reference Antibody (emactuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281592026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-4-sds-page.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (LY3022855)Anti-CSF1R/M-CSFR/CD115 Reference Antibody (LY3022855) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00082-4-sec-hplc.jpgAnti-CSF1R / M-CSFR / CD115 Reference Antibody (LY3022855)The purity of Anti-CSF1R/M-CSFR/CD115 Reference Antibody (LY3022855)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281602026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-4-sds-page.jpgAnti-PCSK9 Reference Antibody (evolocumab)Anti-PCSK9 Reference Antibody (evolocumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-4-sec-hplc.jpgAnti-PCSK9 Reference Antibody (evolocumab)The purity of Anti-PCSK9 Reference Antibody (evolocumab)is more than 97.86% https://www.bosterbio.com/catalog/product/view/id/1281612026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-6-sds-page.jpgAnti-PCSK9 Reference Antibody (recaticimab)Anti-PCSK9 Reference Antibody (recaticimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-6-sec-hplc.jpgAnti-PCSK9 Reference Antibody (recaticimab)The purity of Anti-PCSK9 Reference Antibody (recaticimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281622026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-7-sds-page.jpgAnti-PCSK9 Reference Antibody (ralpancizumab)Anti-PCSK9 Reference Antibody (ralpancizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-7-sec-hplc.jpgAnti-PCSK9 Reference Antibody (ralpancizumab)The purity of Anti-PCSK9 Reference Antibody (ralpancizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281632026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-8-sds-page.jpgAnti-PCSK9 Reference Antibody (RG7652)Anti-PCSK9 Reference Antibody (RG7652) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-8-sec-hplc.jpgAnti-PCSK9 Reference Antibody (RG7652)The purity of Anti-PCSK9 Reference Antibody (RG7652)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281642026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-9-sds-page.jpgAnti-PCSK9 Reference Antibody (lodelcizumab)Anti-PCSK9 Reference Antibody (lodelcizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-9-sec-hplc.jpgAnti-PCSK9 Reference Antibody (lodelcizumab)The purity of Anti-PCSK9 Reference Antibody (lodelcizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281652026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-10-sds-page.jpgAnti-PCSK9 Reference Antibody (ongericimab)Anti-PCSK9 Reference Antibody (ongericimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-10-sec-hplc.jpgAnti-PCSK9 Reference Antibody (ongericimab)The purity of Anti-PCSK9 Reference Antibody (ongericimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281662026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-11-sds-page.jpgAnti-PCSK9 Reference Antibody (tafolecimab)Anti-PCSK9 Reference Antibody (tafolecimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95% https://www.bosterbio.com/catalog/product/view/id/1281672026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-12-sds-page.jpgAnti-PCSK9 Reference Antibody (frovocimab)Anti-PCSK9 Reference Antibody (frovocimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-12-sec-hplc.jpgAnti-PCSK9 Reference Antibody (frovocimab)The purity of Anti-PCSK9 Reference Antibody (frovocimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281682026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-13-sds-page.jpgAnti-PCSK9 Reference Antibody (bococizumab)Anti-PCSK9 Reference Antibody (bococizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-13-sec-hplc.jpgAnti-PCSK9 Reference Antibody (bococizumab)The purity of Anti-PCSK9 Reference Antibody (bococizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281692026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-14-sds-page.jpgAnti-PCSK9 Reference Antibody (ebronucimab)Anti-PCSK9 Reference Antibody (ebronucimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-14-sec-hplc.jpgAnti-PCSK9 Reference Antibody (ebronucimab)The purity of Anti-PCSK9 Reference Antibody (ebronucimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281702026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-15-sds-page.jpgAnti-PCSK9 Reference Antibody (Boehringer anti-PCSK9)Anti-PCSK9 Reference Antibody (Boehringer anti-PCSK9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-15-sec-hplc.jpgAnti-PCSK9 Reference Antibody (Boehringer anti-PCSK9)The purity of Anti-PCSK9 Reference Antibody (Boehringer anti-PCSK9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281712026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-16-sds-page.jpgAnti-PCSK9 Reference Antibody (Merck patent anti-PCSK9)Anti-PCSK9 Reference Antibody (Merck patent anti-PCSK9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-16-sec-hplc.jpgAnti-PCSK9 Reference Antibody (Merck patent anti-PCSK9)The purity of Anti-PCSK9 Reference Antibody (Merck patent anti-PCSK9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281722026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-5-sds-page.jpgAnti-PCSK9 Reference Antibody (Schering patent anti-PCSK9)Anti-PCSK9 Reference Antibody (Schering patent anti-PCSK9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00085-5-sec-hplc.jpgAnti-PCSK9 Reference Antibody (Schering patent anti-PCSK9)The purity of Anti-PCSK9 Reference Antibody (Schering patent anti-PCSK9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281732026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00089-1-sds-page.jpgAnti-HGF / SF Reference Antibody (rilotumumab)Anti-HGF/SF Reference Antibody (rilotumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00089-1-sec-hplc.jpgAnti-HGF / SF Reference Antibody (rilotumumab)The purity of Anti-HGF/SF Reference Antibody (rilotumumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00089-1-od450.jpgAnti-HGF / SF Reference Antibody (rilotumumab)Immobilized human HGF His at 2 &mug/mL can bind Anti-HGF/SF Reference Antibody (rilotumumab) https://www.bosterbio.com/catalog/product/view/id/1281742026-03-10T04:38:48+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00089-2-sds-page.jpgAnti-HGF / SF Reference Antibody (TAK-701)Anti-HGF/SF Reference Antibody (TAK-701) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00089-2-sec-hplc.jpgAnti-HGF / SF Reference Antibody (TAK-701)The purity of Anti-HGF/SF Reference Antibody (TAK-701)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281752026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00089-3-sds-page.jpgAnti-HGF / SF Reference Antibody (ficlatuzumab)Anti-HGF/SF Reference Antibody (ficlatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00089-3-sec-hplc.jpgAnti-HGF / SF Reference Antibody (ficlatuzumab)The purity of Anti-HGF/SF Reference Antibody (ficlatuzumab)is more than 98.01% https://www.bosterbio.com/catalog/product/view/id/1281762026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00096-4-sds-page.jpgAnti-PDGFRB / CD140b Reference Antibody (rinucumab)Anti-PDGFRB/CD140b Reference Antibody (rinucumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00096-4-sec-hplc.jpgAnti-PDGFRB / CD140b Reference Antibody (rinucumab)The purity of Anti-PDGFRB/CD140b Reference Antibody (rinucumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281772026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00096-5-sds-page.jpgAnti-PDGFRB / CD140b Reference Antibody (IMC-2C5)Anti-PDGFRB/CD140b Reference Antibody (IMC-2C5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00096-5-sec-hplc.jpgAnti-PDGFRB / CD140b Reference Antibody (IMC-2C5)The purity of Anti-PDGFRB/CD140b Reference Antibody (IMC-2C5)is more than 99.79% https://www.bosterbio.com/catalog/product/view/id/1281782026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-6-sds-page.jpgAnti-Tau Reference Antibody (zagotenemab)Anti-Tau Reference Antibody (zagotenemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-6-sec-hplc.jpgAnti-Tau Reference Antibody (zagotenemab)The purity of Anti-Tau Reference Antibody (zagotenemab)is more than 98.97% https://www.bosterbio.com/catalog/product/view/id/1281792026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-7-sds-page.jpgAnti-Tau Reference Antibody (tilavonemab)Anti-Tau Reference Antibody (tilavonemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-7-sec-hplc.jpgAnti-Tau Reference Antibody (tilavonemab)The purity of Anti-Tau Reference Antibody (tilavonemab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281802026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-8-sds-page.jpgAnti-Tau Reference Antibody (semorinemab)Anti-Tau Reference Antibody (semorinemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-8-sec-hplc.jpgAnti-Tau Reference Antibody (semorinemab)The purity of Anti-Tau Reference Antibody (semorinemab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281812026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-9-sds-page.jpgAnti-Tau Reference Antibody (bepranemab)Anti-Tau Reference Antibody (bepranemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-9-sec-hplc.jpgAnti-Tau Reference Antibody (bepranemab)The purity of Anti-Tau Reference Antibody (bepranemab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281822026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-10-sds-page.jpgAnti-Tau Reference Antibody (gosuranemab)Anti-Tau Reference Antibody (gosuranemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00097-10-sec-hplc.jpgAnti-Tau Reference Antibody (gosuranemab)The purity of Anti-Tau Reference Antibody (gosuranemab)is more than 97.31% https://www.bosterbio.com/catalog/product/view/id/1281832026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-4-sds-page.jpgAnti-FGFR1 / CD331 Reference Antibody (Lilly patent anti-FGFR-1)Anti-FGFR1/CD331 Reference Antibody (Lilly patent anti-FGFR-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00098-4-sec-hplc.jpgAnti-FGFR1 / CD331 Reference Antibody (Lilly patent anti-FGFR-1)The purity of Anti-FGFR1/CD331 Reference Antibody (Lilly patent anti-FGFR-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281842026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-7-sds-page.jpgAnti-IL-1b Reference Antibody (gevokizumab)Anti-IL-1b Reference Antibody (gevokizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-7-sec-hplc.jpgAnti-IL-1b Reference Antibody (gevokizumab)The purity of Anti-IL-1b Reference Antibody (gevokizumab)is more than 98.81% https://www.bosterbio.com/catalog/product/view/id/1281852026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-6-sds-page.jpgAnti-IL-1b Reference Antibody (CDP484)Anti-IL-1b Reference Antibody (CDP484) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00101-6-sec-hplc.jpgAnti-IL-1b Reference Antibody (CDP484)The purity of Anti-IL-1b Reference Antibody (CDP484)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281862026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-4-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (sirukumab)Anti-IL-6/IFNb2 Reference Antibody (sirukumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-4-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (sirukumab)The purity of Anti-IL-6/IFNb2 Reference Antibody (sirukumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-4-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (sirukumab)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (sirukumab) https://www.bosterbio.com/catalog/product/view/id/1281872026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-5-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (Chugai SK2)Anti-IL-6/IFNb2 Reference Antibody (Chugai SK2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-5-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (Chugai SK2)The purity of Anti-IL-6/IFNb2 Reference Antibody (Chugai SK2)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-5-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (Chugai SK2)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (Chugai SK2) https://www.bosterbio.com/catalog/product/view/id/1281882026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-6-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (MEDI 5117)Anti-IL-6/IFNb2 Reference Antibody (MEDI 5117) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-6-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (MEDI 5117)The purity of Anti-IL-6/IFNb2 Reference Antibody (MEDI 5117)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-6-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (MEDI 5117)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (MEDI 5117) https://www.bosterbio.com/catalog/product/view/id/1281892026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-7-sds-page.jpgAnti-IL-6Ra / CD126 Reference Antibody (vobarilizumab)Anti-IL-6Ra/CD126 Reference Antibody (vobarilizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 96.9%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-7-sec-hplc.jpgAnti-IL-6Ra / CD126 Reference Antibody (vobarilizumab)The purity of Anti-IL-6Ra/CD126 Reference Antibody (vobarilizumab)is more than 99.34%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-7-od450.jpgAnti-IL-6Ra / CD126 Reference Antibody (vobarilizumab)Immobilized human IL 6R His at 2 &mug/mL can bind Anti-IL-6Ra/CD126 Reference Antibody (vobarilizumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-7-facs.jpgAnti-IL-6Ra / CD126 Reference Antibody (vobarilizumab)Human IL6R CHO cells were stained with Anti-IL-6Ra/CD126 Reference Antibody (vobarilizumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1281902026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-8-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (elsilimomab)Anti-IL-6/IFNb2 Reference Antibody (elsilimomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-8-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (elsilimomab)The purity of Anti-IL-6/IFNb2 Reference Antibody (elsilimomab)is more than 98.96%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-8-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (elsilimomab)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (elsilimomab) https://www.bosterbio.com/catalog/product/view/id/1281912026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-9-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (siltuximab)Anti-IL-6/IFNb2 Reference Antibody (siltuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-9-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (siltuximab)The purity of Anti-IL-6/IFNb2 Reference Antibody (siltuximab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-9-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (siltuximab)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (siltuximab) https://www.bosterbio.com/catalog/product/view/id/1281922026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-10-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (olokizumab)Anti-IL-6/IFNb2 Reference Antibody (olokizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-10-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (olokizumab)The purity of Anti-IL-6/IFNb2 Reference Antibody (olokizumab)is more than 99.07%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-10-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (olokizumab)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (olokizumab) https://www.bosterbio.com/catalog/product/view/id/1281932026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-11-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (CSTRI patent anti-IL-6)Anti-IL-6/IFNb2 Reference Antibody (CSTRI patent anti-IL-6) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-11-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (CSTRI patent anti-IL-6)The purity of Anti-IL-6/IFNb2 Reference Antibody (CSTRI patent anti-IL-6)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-11-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (CSTRI patent anti-IL-6)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (CSTRI patent anti-IL-6) https://www.bosterbio.com/catalog/product/view/id/1281942026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-12-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (Medarex patent anti-IL-6)Anti-IL-6/IFNb2 Reference Antibody (Medarex patent anti-IL-6) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-12-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (Medarex patent anti-IL-6)The purity of Anti-IL-6/IFNb2 Reference Antibody (Medarex patent anti-IL-6)is more than 99.56%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-12-od450.jpgAnti-IL-6 / IFNb2 Reference Antibody (Medarex patent anti-IL-6)Immobilized human IL-6 His at 2 &mug/mL can bind Anti-IL-6/IFNb2 Reference Antibody (Medarex patent anti-IL-6) https://www.bosterbio.com/catalog/product/view/id/1281952026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-13-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (ziltivekimab)Anti-IL-6/IFNb2 Reference Antibody (ziltivekimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-13-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (ziltivekimab)The purity of Anti-IL-6/IFNb2 Reference Antibody (ziltivekimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281962026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-14-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (clazakizumab)Anti-IL-6/IFNb2 Reference Antibody (clazakizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-14-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (clazakizumab)The purity of Anti-IL-6/IFNb2 Reference Antibody (clazakizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1281972026-03-10T04:38:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-15-sds-page.jpgAnti-IL-6 / IFNb2 Reference Antibody (Merck patent anti-IL-6)Anti-IL-6/IFNb2 Reference Antibody (Merck patent anti-IL-6) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00102-15-sec-hplc.jpgAnti-IL-6 / IFNb2 Reference Antibody (Merck patent anti-IL-6)The purity of Anti-IL-6/IFNb2 Reference Antibody (Merck patent anti-IL-6)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1281982026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-7-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (avelumab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (avelumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-7-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (avelumab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (avelumab)is more than 98.22%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-7-od450.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (avelumab)Immobilized human PD L1 FC at 2 &mug/mL can bind Anti-B7-H1/PD-L1/CD274 Reference Antibody (avelumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-7-syngenic-mc38-moel.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (avelumab)Avelumab inhibited the tumor growth of MC38 on hLAG3 mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1281992026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-9-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (envafolimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (envafolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-9-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (envafolimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (envafolimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-9-od450.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (envafolimab)Immobilized human PD L1 His at 2 &mug/mL can bind Anti-B7-H1/PD-L1/CD274 Reference Antibody (envafolimab) https://www.bosterbio.com/catalog/product/view/id/1282002026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-10-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (sugemalimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (sugemalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-10-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (sugemalimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (sugemalimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-10-od450.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (sugemalimab)Immobilized human PD L1 His at 2 &mug/mL can bind Anti-B7-H1/PD-L1/CD274 Reference Antibody (sugemalimab) https://www.bosterbio.com/catalog/product/view/id/1282012026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-11-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (pacmilimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (pacmilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-11-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (pacmilimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (pacmilimab)is more than 96.16% https://www.bosterbio.com/catalog/product/view/id/1282022026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-12-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (MDX-1105)Anti-B7-H1/PD-L1/CD274 Reference Antibody (MDX-1105) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-12-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (MDX-1105)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (MDX-1105)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282032026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-13-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (manelimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (manelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-13-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (manelimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (manelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282042026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-14-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (lodapolimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (lodapolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-14-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (lodapolimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (lodapolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282052026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-15-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (Lesabelimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (Lesabelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-15-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (Lesabelimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (Lesabelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282062026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-16-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (adebrelimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (adebrelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-16-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (adebrelimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (adebrelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282072026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-17-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (sudubrilimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (sudubrilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-17-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (sudubrilimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (sudubrilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282082026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-18-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (opucolimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (opucolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-18-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (opucolimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (opucolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282092026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-19-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (garivulimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (garivulimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-19-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (garivulimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (garivulimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282102026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-20-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (cosibelimab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (cosibelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-20-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (cosibelimab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (cosibelimab)is more than 99.9% https://www.bosterbio.com/catalog/product/view/id/1282112026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-8-sds-page.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (durvalumab)Anti-B7-H1/PD-L1/CD274 Reference Antibody (durvalumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-8-sec-hplc.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (durvalumab)The purity of Anti-B7-H1/PD-L1/CD274 Reference Antibody (durvalumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00109-8-xenograft-pd-l1-a375-pbmc-model.jpgAnti-B7-H1 / PD-L1 / CD274 Reference Antibody (durvalumab)Durvalumab inhibited the tumor growth of A375 on NOD.SCID mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1282122026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-3-sds-page.jpgAnti-IL-33 Reference Antibody (etokimab)Anti-IL-33 Reference Antibody (etokimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-3-sec-hplc.jpgAnti-IL-33 Reference Antibody (etokimab)The purity of Anti-IL-33 Reference Antibody (etokimab)is more than 99.76%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-3-od450.jpgAnti-IL-33 Reference Antibody (etokimab)Immobilized human IL 33 His at 2 &mug/mL can bind Anti-IL-33 Reference Antibody (etokimab) https://www.bosterbio.com/catalog/product/view/id/1282132026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-4-sds-page.jpgAnti-IL-33 Reference Antibody (tozorakimab)Anti-IL-33 Reference Antibody (tozorakimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-4-sec-hplc.jpgAnti-IL-33 Reference Antibody (tozorakimab)The purity of Anti-IL-33 Reference Antibody (tozorakimab)is more than 99.21%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-4-od450.jpgAnti-IL-33 Reference Antibody (tozorakimab)Immobilized human IL 33 His at 2 &mug/mL can bind Anti-IL-33 Reference Antibody (tozorakimab) https://www.bosterbio.com/catalog/product/view/id/1282142026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-5-sds-page.jpgAnti-IL-33 Reference Antibody (itepekimab)Anti-IL-33 Reference Antibody (itepekimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-5-sec-hplc.jpgAnti-IL-33 Reference Antibody (itepekimab)The purity of Anti-IL-33 Reference Antibody (itepekimab)is more than 97.5% https://www.bosterbio.com/catalog/product/view/id/1282152026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-6-sds-page.jpgAnti-IL-33 Reference Antibody (torudokimab)Anti-IL-33 Reference Antibody (torudokimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00113-6-sec-hplc.jpgAnti-IL-33 Reference Antibody (torudokimab)The purity of Anti-IL-33 Reference Antibody (torudokimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282162026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00121-4-sds-page.jpgAnti-FGF2 Reference Antibody (HuGAL-F2)Anti-FGF2 Reference Antibody (HuGAL-F2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00121-4-sec-hplc.jpgAnti-FGF2 Reference Antibody (HuGAL-F2)The purity of Anti-FGF2 Reference Antibody (HuGAL-F2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282172026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-1-sds-page.jpgAnti-IL-18 Reference Antibody (Camoteskimab)Anti-IL-18 Reference Antibody (Camoteskimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-1-sec-hplc.jpgAnti-IL-18 Reference Antibody (Camoteskimab)The purity of Anti-IL-18 Reference Antibody (Camoteskimab)is more than 98.41%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-1-od450.jpgAnti-IL-18 Reference Antibody (Camoteskimab)Immobilized human IL 18 C His at 2 &mug/mL can bind Anti-IL-18 Reference Antibody (Camoteskimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-1-facs.jpgAnti-IL-18 Reference Antibody (Camoteskimab)Anti-IL-18 Reference Antibody (Camoteskimab)-induced FACS Blocking activity was evaluated using Hu IL-18Ralpha&IL-18Rbeta HEK293-. The IC50 was approximately 0.172 &mug/mL. https://www.bosterbio.com/catalog/product/view/id/1282182026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-2-sds-page.jpgAnti-IL-18 Reference Antibody (GSK 1070806)Anti-IL-18 Reference Antibody (GSK 1070806) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-2-sec-hplc.jpgAnti-IL-18 Reference Antibody (GSK 1070806)The purity of Anti-IL-18 Reference Antibody (GSK 1070806)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-2-facs.jpgAnti-IL-18 Reference Antibody (GSK 1070806)Anti-IL-18 Reference Antibody (GSK 1070806)-induced FACS Blocking activity was evaluated using Hu IL-18Ralpha-Hu IL-18Rbeta-HEK293-A8. The IC50 was approximately 0.335 &mug/mL. https://www.bosterbio.com/catalog/product/view/id/1282192026-03-10T04:38:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-3-sds-page.jpgAnti-IL-18 Reference Antibody (ABT-325)Anti-IL-18 Reference Antibody (ABT-325) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00124-3-sec-hplc.jpgAnti-IL-18 Reference Antibody (ABT-325)The purity of Anti-IL-18 Reference Antibody (ABT-325)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282202026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00131-2-sds-page.jpgAnti-TLR2 / CD282 Reference Antibody (tomaralimab)Anti-TLR2/CD282 Reference Antibody (tomaralimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00131-2-sec-hplc.jpgAnti-TLR2 / CD282 Reference Antibody (tomaralimab)The purity of Anti-TLR2/CD282 Reference Antibody (tomaralimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1282212026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-3-sds-page.jpgAnti-CD14 Reference Antibody (atibuclimab)Anti-CD14 Reference Antibody (atibuclimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-3-sec-hplc.jpgAnti-CD14 Reference Antibody (atibuclimab)The purity of Anti-CD14 Reference Antibody (atibuclimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00137-3-od450.jpgAnti-CD14 Reference Antibody (atibuclimab)Immobilized human CD14 https://www.bosterbio.com/catalog/product/view/id/1282222026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-2-sds-page.jpgAnti-MMP9 Reference Antibody (andecaliximab)Anti-MMP9 Reference Antibody (andecaliximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-2-sec-hplc.jpgAnti-MMP9 Reference Antibody (andecaliximab)The purity of Anti-MMP9 Reference Antibody (andecaliximab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-2-od450.jpgAnti-MMP9 Reference Antibody (andecaliximab)Immobilized human MMP9 His at 2 &mug/mL can bind Anti-MMP9 Reference Antibody (andecaliximab) https://www.bosterbio.com/catalog/product/view/id/1282232026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-3-sds-page.jpgAnti-MMP9 Reference Antibody (Yeda patent anti-MMP-9)Anti-MMP9 Reference Antibody (Yeda patent anti-MMP-9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00139-3-sec-hplc.jpgAnti-MMP9 Reference Antibody (Yeda patent anti-MMP-9)The purity of Anti-MMP9 Reference Antibody (Yeda patent anti-MMP-9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282242026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00148-3-sds-page.jpgAnti-IGF-1 Reference Antibody (xentuzumab)Anti-IGF-1 Reference Antibody (xentuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95.3%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00148-3-sec-hplc.jpgAnti-IGF-1 Reference Antibody (xentuzumab)The purity of Anti-IGF-1 Reference Antibody (xentuzumab)is more than 98.72%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00148-3-od450.jpgAnti-IGF-1 Reference Antibody (xentuzumab)Immobilized human IGF I Protein https://www.bosterbio.com/catalog/product/view/id/1282252026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-6-sds-page.jpgAnti-CD19 Reference Antibody (denintuzumab-MMAF)Anti-CD19 Reference Antibody (denintuzumab-MMAF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-6-sec-hplc.jpgAnti-CD19 Reference Antibody (denintuzumab-MMAF)The purity of Anti-CD19 Reference Antibody (denintuzumab-MMAF)is more than 99.58%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-6-od450.jpgAnti-CD19 Reference Antibody (denintuzumab-MMAF)Immobilized human EGFR His at 2 &mug/mL can bind Anti-CD19 Reference Antibody (denintuzumab-MMAF) https://www.bosterbio.com/catalog/product/view/id/1282262026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-7-sds-page.jpgAnti-CD19 Reference Antibody (Loncastuximab tesirine)Anti-CD19 Reference Antibody (Loncastuximab tesirine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-7-sec-hplc.jpgAnti-CD19 Reference Antibody (Loncastuximab tesirine)The purity of Anti-CD19 Reference Antibody (Loncastuximab tesirine)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1282272026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-8-sds-page.jpgAnti-CD19 Reference Antibody (Loncastuximab)Anti-CD19 Reference Antibody (Loncastuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-8-sec-hplc.jpgAnti-CD19 Reference Antibody (Loncastuximab)The purity of Anti-CD19 Reference Antibody (Loncastuximab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1282282026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-9-sds-page.jpgAnti-CD19 Reference Antibody (tafasitamab)Anti-CD19 Reference Antibody (tafasitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-9-sec-hplc.jpgAnti-CD19 Reference Antibody (tafasitamab)The purity of Anti-CD19 Reference Antibody (tafasitamab)is more than 98.59%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-9-od450.jpgAnti-CD19 Reference Antibody (tafasitamab)Immobilized human CD19 (20 291) Proteinhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-9-facs.jpgAnti-CD19 Reference Antibody (tafasitamab)Human CD19 HEK293 cells were stained with Anti-CD19 Reference Antibody (tafasitamab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1282292026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-10-sds-page.jpgAnti-CD19 Reference Antibody (inebilizumab)Anti-CD19 Reference Antibody (inebilizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-10-sec-hplc.jpgAnti-CD19 Reference Antibody (inebilizumab)The purity of Anti-CD19 Reference Antibody (inebilizumab)is more than 98.79% https://www.bosterbio.com/catalog/product/view/id/1282302026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-11-sds-page.jpgAnti-CD19 Reference Antibody (denintuzumab)Anti-CD19 Reference Antibody (denintuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-11-sec-hplc.jpgAnti-CD19 Reference Antibody (denintuzumab)The purity of Anti-CD19 Reference Antibody (denintuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1282312026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-12-sds-page.jpgAnti-CD19 Reference Antibody (obexelimab)Anti-CD19 Reference Antibody (obexelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-12-sec-hplc.jpgAnti-CD19 Reference Antibody (obexelimab)The purity of Anti-CD19 Reference Antibody (obexelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282322026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-13-sds-page.jpgAnti-CD19 Reference Antibody (coltuximab)Anti-CD19 Reference Antibody (coltuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-13-sec-hplc.jpgAnti-CD19 Reference Antibody (coltuximab)The purity of Anti-CD19 Reference Antibody (coltuximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282332026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-14-sds-page.jpgAnti-CD19 Reference Antibody (Duke U. patent anti-CD19)Anti-CD19 Reference Antibody (Duke U. patent anti-CD19) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-14-sec-hplc.jpgAnti-CD19 Reference Antibody (Duke U. patent anti-CD19)The purity of Anti-CD19 Reference Antibody (Duke U. patent anti-CD19)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282342026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-15-sds-page.jpgAnti-CD19 Reference Antibody (Immunomedics hA19)Anti-CD19 Reference Antibody (Immunomedics hA19) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00154-15-sec-hplc.jpgAnti-CD19 Reference Antibody (Immunomedics hA19)The purity of Anti-CD19 Reference Antibody (Immunomedics hA19)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282352026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-sds-page.jpgAnti-Complement C5 Reference Antibody (ravulizumab)Anti-Complement C5 Reference Antibody (ravulizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-sec-hplc.jpgAnti-Complement C5 Reference Antibody (ravulizumab)The purity of Anti-Complement C5 Reference Antibody (ravulizumab)is more than 98.96%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-od450.jpgAnti-Complement C5 Reference Antibody (ravulizumab)Immobilized human C5 His at 2 &mug/mL can bind Anti-Complement C5 Reference Antibody (ravulizumab) https://www.bosterbio.com/catalog/product/view/id/1282362026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-1-sds-page.jpgAnti-Complement C5 Reference Antibody (eculizumab)Anti-Complement C5 Reference Antibody (eculizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-1-sec-hplc.jpgAnti-Complement C5 Reference Antibody (eculizumab)The purity of Anti-Complement C5 Reference Antibody (eculizumab)is more than 98.7%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-1-od450.jpgAnti-Complement C5 Reference Antibody (eculizumab)Immobilized human CO5 His at 2 &mug/mL can bind Anti-Complement C5 Reference Antibody (eculizumab) https://www.bosterbio.com/catalog/product/view/id/1282372026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-2-sds-page.jpgAnti-Complement C5 Reference Antibody (tesidolumab)Anti-Complement C5 Reference Antibody (tesidolumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-2-sec-hplc.jpgAnti-Complement C5 Reference Antibody (tesidolumab)The purity of Anti-Complement C5 Reference Antibody (tesidolumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282382026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-3-sds-page.jpgAnti-Complement C5 Reference Antibody (crovalimab)Anti-Complement C5 Reference Antibody (crovalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-3-sec-hplc.jpgAnti-Complement C5 Reference Antibody (crovalimab)The purity of Anti-Complement C5 Reference Antibody (crovalimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282392026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-4-sds-page.jpgAnti-Complement C5 Reference Antibody (lendalizumab)Anti-Complement C5 Reference Antibody (lendalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-4-sec-hplc.jpgAnti-Complement C5 Reference Antibody (lendalizumab)The purity of Anti-Complement C5 Reference Antibody (lendalizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282402026-03-10T04:38:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-5-sds-page.jpgAnti-Complement C5 Reference Antibody (pozelimab)Anti-Complement C5 Reference Antibody (pozelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-5-sec-hplc.jpgAnti-Complement C5 Reference Antibody (pozelimab)The purity of Anti-Complement C5 Reference Antibody (pozelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282412026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-6-sds-page.jpgAnti-Complement C5 Reference Antibody (vilobelimab)Anti-Complement C5 Reference Antibody (vilobelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00156-6-sec-hplc.jpgAnti-Complement C5 Reference Antibody (vilobelimab)The purity of Anti-Complement C5 Reference Antibody (vilobelimab)is more than 99.27% https://www.bosterbio.com/catalog/product/view/id/1282422026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00158-3-sds-page.jpgAnti-CCR2 / CD192 Reference Antibody (plozalizumab)Anti-CCR2/CD192 Reference Antibody (plozalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00158-3-sec-hplc.jpgAnti-CCR2 / CD192 Reference Antibody (plozalizumab)The purity of Anti-CCR2/CD192 Reference Antibody (plozalizumab)is more than 99.45% https://www.bosterbio.com/catalog/product/view/id/1282432026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00162-1-sds-page.jpgAnti-Serum Amyloid P / SAP Reference Antibody (dezamizumab)Anti-Serum Amyloid P/SAP Reference Antibody (dezamizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00162-1-sec-hplc.jpgAnti-Serum Amyloid P / SAP Reference Antibody (dezamizumab)The purity of Anti-Serum Amyloid P/SAP Reference Antibody (dezamizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282442026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00164-sds-page.jpgAnti-IL-17c Reference Antibody (MOR106)Anti-IL-17c Reference Antibody (MOR106) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00164-sec-hplc.jpgAnti-IL-17c Reference Antibody (MOR106)The purity of Anti-IL-17c Reference Antibody (MOR106)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282452026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00168-7-sds-page.jpgAnti-Complement C3 Reference Antibody (NGM621)Anti-Complement C3 Reference Antibody (NGM621) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00168-7-sec-hplc.jpgAnti-Complement C3 Reference Antibody (NGM621)The purity of Anti-Complement C3 Reference Antibody (NGM621)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282462026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-6-sds-page.jpgAnti-ICAM1 / CD54 Reference Antibody (Enlimomab)Anti-ICAM1/CD54 Reference Anticody (Enlimomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-6-sec-hplc.jpgAnti-ICAM1 / CD54 Reference Antibody (Enlimomab)The purity of Anti-ICAM1/CD54 Reference Anticody (Enlimomab)is more than 97.77% https://www.bosterbio.com/catalog/product/view/id/1282472026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-7-sds-page.jpgAnti-ICAM1 / CD54 Reference Antibody (bersanlimab)Anti-ICAM1/CD54 Reference Antibody (bersanlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95.0%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00171-7-sec-hplc.jpgAnti-ICAM1 / CD54 Reference Antibody (bersanlimab)The purity of Anti-ICAM1/CD54 Reference Antibody (bersanlimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1282482026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-7-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (toripalimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (toripalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-7-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (toripalimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (toripalimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-7-od450.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (toripalimab)Immobilized human PD 1(C 6His) at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (toripalimab) https://www.bosterbio.com/catalog/product/view/id/1282492026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-8-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (nivolumab)Anti-PDCD1/PD-1/CD279 Reference Antibody (nivolumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-8-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (nivolumab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (nivolumab)is more than 99.03%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-8-od450.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (nivolumab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (nivolumab) https://www.bosterbio.com/catalog/product/view/id/1282502026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-9-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (sintilimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (sintilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-9-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (sintilimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (sintilimab)is more than 98.24%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-9-od450.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (sintilimab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (sintilimab) https://www.bosterbio.com/catalog/product/view/id/1282512026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-10-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (camrelizumab)Anti-PDCD1/PD-1/CD279 Reference Antibody (camrelizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-10-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (camrelizumab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (camrelizumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-10-od450.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (camrelizumab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (camrelizumab) https://www.bosterbio.com/catalog/product/view/id/1282522026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-11-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (spartalizumab)Anti-PDCD1/PD-1/CD279 Reference Antibody (spartalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-11-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (spartalizumab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (spartalizumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-11-od450.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (spartalizumab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (spartalizumab) https://www.bosterbio.com/catalog/product/view/id/1282532026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-12-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (serplulimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (serplulimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-12-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (serplulimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (serplulimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-12-od450.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (serplulimab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (serplulimab) https://www.bosterbio.com/catalog/product/view/id/1282542026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-14-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (cemiplimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (cemiplimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-14-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (cemiplimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (cemiplimab)is more than 100.00%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-14-od450.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (cemiplimab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-PDCD1/PD-1/CD279 Reference Antibody (cemiplimab) https://www.bosterbio.com/catalog/product/view/id/1282552026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-15-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (tislelizumab)Anti-PDCD1/PD-1/CD279 Reference Antibody (tislelizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-15-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (tislelizumab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (tislelizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282562026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-16-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (dostarlimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (dostarlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-16-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (dostarlimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (dostarlimab)is more than 99.31% https://www.bosterbio.com/catalog/product/view/id/1282572026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-17-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (finotonlimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (finotonlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-17-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (finotonlimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (finotonlimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282582026-03-10T04:38:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-18-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (retifanlimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (retifanlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-18-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (retifanlimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (retifanlimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282592026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-19-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (geptanolimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (geptanolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-19-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (geptanolimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (geptanolimab)is more than 97.72% https://www.bosterbio.com/catalog/product/view/id/1282602026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-20-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (iparomlimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (iparomlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-20-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (iparomlimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (iparomlimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282612026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-21-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (pidilizumab)Anti-PDCD1/PD-1/CD279 Reference Antibody (pidilizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-21-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (pidilizumab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (pidilizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282622026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-22-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (sasanlimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (sasanlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-22-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (sasanlimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (sasanlimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282632026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-23-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (pimivalimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (pimivalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-23-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (pimivalimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (pimivalimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282642026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-24-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (zimberelimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (zimberelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-24-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (zimberelimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (zimberelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282652026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-25-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (prolgolimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (prolgolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-25-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (prolgolimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (prolgolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282662026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-26-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (Rulonilimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (Rulonilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-26-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (Rulonilimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (Rulonilimab)is more than 98.65% https://www.bosterbio.com/catalog/product/view/id/1282672026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-27-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (nofazinlimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (nofazinlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-27-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (nofazinlimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (nofazinlimab)is more than 98.2% https://www.bosterbio.com/catalog/product/view/id/1282682026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-28-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (cetrelimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (cetrelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-28-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (cetrelimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (cetrelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282692026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-29-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (budigalimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (budigalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-29-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (budigalimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (budigalimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282702026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-30-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (ezabenlimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (ezabenlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-30-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (ezabenlimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (ezabenlimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282712026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-31-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (Rosnilimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (Rosnilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-31-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (Rosnilimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (Rosnilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282722026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-32-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (penpulimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (penpulimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-32-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (penpulimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (penpulimab)is more than 96.8% https://www.bosterbio.com/catalog/product/view/id/1282732026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-33-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (balstilimab)Anti-PDCD1/PD-1/CD279 Reference Antibody (balstilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-33-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (balstilimab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (balstilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282742026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-34-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (Peresolomab)Anti-PDCD1/PD-1/CD279 Reference Antibody (Peresolomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-34-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (Peresolomab)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (Peresolomab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282752026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-13-sds-page.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (UCB patent anti-PD-1)Anti-PDCD1/PD-1/CD279 Reference Antibody (UCB patent anti-PD-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00178-13-sec-hplc.jpgAnti-PDCD1 / PD-1 / CD279 Reference Antibody (UCB patent anti-PD-1)The purity of Anti-PDCD1/PD-1/CD279 Reference Antibody (UCB patent anti-PD-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282762026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-5-sds-page.jpgAnti-Bcl-2 Reference Antibody (U.Toronto patent anti-Bax)Anti-Bcl-2 Reference Antibody (U.Toronto patent anti-Bax) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00183-5-sec-hplc.jpgAnti-Bcl-2 Reference Antibody (U.Toronto patent anti-Bax)The purity of Anti-Bcl-2 Reference Antibody (U.Toronto patent anti-Bax)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282772026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-4-sds-page.jpgAnti-NCAM1 / CD56 Reference Antibody (lorvotuzumab mertansine)Anti-NCAM1/CD56 Reference Antibody (lorvotuzumab mertansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-4-sec-hplc.jpgAnti-NCAM1 / CD56 Reference Antibody (lorvotuzumab mertansine)The purity of Anti-NCAM1/CD56 Reference Antibody (lorvotuzumab mertansine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282782026-03-10T04:38:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-5-sds-page.jpgAnti-NCAM1 / CD56 Reference Antibody (lorvotuzumab)Anti-NCAM1/CD56 Reference Antibody (lorvotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-5-sec-hplc.jpgAnti-NCAM1 / CD56 Reference Antibody (lorvotuzumab)The purity of Anti-NCAM1/CD56 Reference Antibody (lorvotuzumab)is more than 99.72% https://www.bosterbio.com/catalog/product/view/id/1282792026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-6-sds-page.jpgAnti-NCAM1 / CD56 Reference Antibody (lorvotuzumab-MMAE)Anti-NCAM1/CD56 Reference Antibody (lorvotuzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00184-6-sec-hplc.jpgAnti-NCAM1 / CD56 Reference Antibody (lorvotuzumab-MMAE)The purity of Anti-NCAM1/CD56 Reference Antibody (lorvotuzumab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282802026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-3-sds-page.jpgAnti-MUC1 Reference Antibody (clivatuzumab)Anti-MUC1 Reference Antibody (clivatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-3-sec-hplc.jpgAnti-MUC1 Reference Antibody (clivatuzumab)The purity of Anti-MUC1 Reference Antibody (clivatuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1282812026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-4-sds-page.jpgAnti-MUC1 Reference Antibody (gatipotuzumab)Anti-MUC1 Reference Antibody (gatipotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-4-sec-hplc.jpgAnti-MUC1 Reference Antibody (gatipotuzumab)The purity of Anti-MUC1 Reference Antibody (gatipotuzumab)is more than 95.15% https://www.bosterbio.com/catalog/product/view/id/1282822026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-5-sds-page.jpgAnti-MUC1 Reference Antibody (AR20.5)Anti-MUC1 Reference Antibody (AR20.5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-5-sec-hplc.jpgAnti-MUC1 Reference Antibody (AR20.5)The purity of Anti-MUC1 Reference Antibody (AR20.5)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282832026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-6-sds-page.jpgAnti-MUC1 Reference Antibody (cantuzumab)Anti-MUC1 Reference Antibody (cantuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-6-sec-hplc.jpgAnti-MUC1 Reference Antibody (cantuzumab)The purity of Anti-MUC1 Reference Antibody (cantuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1282842026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-7-sds-page.jpgAnti-MUC1 Reference Antibody (clivatuzumab-MMAE)Anti-MUC1 Reference Antibody (clivatuzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00187-7-sec-hplc.jpgAnti-MUC1 Reference Antibody (clivatuzumab-MMAE)The purity of Anti-MUC1 Reference Antibody (clivatuzumab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282852026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00188-1-sds-page.jpgAnti-FLT3 / CD135 Reference Antibody (IMC-EB10)Anti-FLT3/CD135 Reference Antibody (IMC-EB10) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00188-1-sec-hplc.jpgAnti-FLT3 / CD135 Reference Antibody (IMC-EB10)The purity of Anti-FLT3/CD135 Reference Antibody (IMC-EB10)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282862026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-3-sds-page.jpgAnti-CD38 Reference Antibody (isatuximab)Anti-CD38 Reference Antibody (isatuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-3-sec-hplc.jpgAnti-CD38 Reference Antibody (isatuximab)The purity of Anti-CD38 Reference Antibody (isatuximab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-3-od450.jpgAnti-CD38 Reference Antibody (isatuximab)Immobilized human CD38 Nhis at 2 &mug/mL can bind Anti-CD38 Reference Antibody (isatuximab) https://www.bosterbio.com/catalog/product/view/id/1282872026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-4-sds-page.jpgAnti-CD38 Reference Antibody (daratumumab)Anti-CD38 Reference Antibody (daratumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-4-sec-hplc.jpgAnti-CD38 Reference Antibody (daratumumab)The purity of Anti-CD38 Reference Antibody (daratumumab)is more than 98.99%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-4-od450.jpgAnti-CD38 Reference Antibody (daratumumab)Immobilized human CD38 NHis at 2 &mug/mL can bind Anti-CD38 Reference Antibody (daratumumab) https://www.bosterbio.com/catalog/product/view/id/1282882026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-5-sds-page.jpgAnti-CD38 Reference Antibody (mezagitamab)Anti-CD38 Reference Antibody (mezagitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-5-sec-hplc.jpgAnti-CD38 Reference Antibody (mezagitamab)The purity of Anti-CD38 Reference Antibody (mezagitamab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-5-od450.jpgAnti-CD38 Reference Antibody (mezagitamab)Immobilized human CD38 NHis at 2 &mug/mL can bind Anti-CD38 Reference Antibody (mezagitamab) https://www.bosterbio.com/catalog/product/view/id/1282892026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-6-sds-page.jpgAnti-CD38 Reference Antibody (felzartamab)Anti-CD38 Reference Antibody (felzartamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00193-6-sec-hplc.jpgAnti-CD38 Reference Antibody (felzartamab)The purity of Anti-CD38 Reference Antibody (felzartamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282902026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00196-5-sds-page.jpgAnti-CD28L / CD80 Reference Antibody (galiximab)Anti-CD28L/CD80 Reference Antibody (galiximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00196-5-sec-hplc.jpgAnti-CD28L / CD80 Reference Antibody (galiximab)The purity of Anti-CD28L/CD80 Reference Antibody (galiximab)is more than 95.08% https://www.bosterbio.com/catalog/product/view/id/1282912026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00197-sds-page.jpgAnti-TLR3 / CD283 Reference Antibody (CNTO5429)Anti-TLR3/CD283 Reference Antibody (CNTO5429) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00197-sec-hplc.jpgAnti-TLR3 / CD283 Reference Antibody (CNTO5429)The purity of Anti-TLR3/CD283 Reference Antibody (CNTO5429)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282922026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-5-sds-page.jpgAnti-FGFR3 / CD333 Reference Antibody (vofatamab)Anti-FGFR3/CD333 Reference Antibody (vofatamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-5-sec-hplc.jpgAnti-FGFR3 / CD333 Reference Antibody (vofatamab)The purity of Anti-FGFR3/CD333 Reference Antibody (vofatamab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-5-od450.jpgAnti-FGFR3 / CD333 Reference Antibody (vofatamab)Immobilized human FGFR3IIIb His at 2 &mug/mL can bind Anti-FGFR3/CD333 Reference Antibody (vofatamab) https://www.bosterbio.com/catalog/product/view/id/1282932026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-6-sds-page.jpgAnti-FGFR3 / CD333 Reference Antibody (LY3076226)Anti-FGFR3/CD333 Reference Antibody (LY3076226) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00200-6-sec-hplc.jpgAnti-FGFR3 / CD333 Reference Antibody (LY3076226)The purity of Anti-FGFR3/CD333 Reference Antibody (LY3076226)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282942026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00212-2-sds-page.jpgAnti-IL-15 Reference Antibody (ordesekimab)Anti-IL-15 Reference Antibody (ordesekimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00212-2-sec-hplc.jpgAnti-IL-15 Reference Antibody (ordesekimab)The purity of Anti-IL-15 Reference Antibody (ordesekimab)is more than 95.77% https://www.bosterbio.com/catalog/product/view/id/1282952026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00212-3-sds-page.jpgAnti-IL-15 Reference Antibody (DISC0280)Anti-IL-15 Reference Antibody (DISC0280) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00212-3-sec-hplc.jpgAnti-IL-15 Reference Antibody (DISC0280)The purity of Anti-IL-15 Reference Antibody (DISC0280)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282962026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-3-sds-page.jpgAnti-IL-2Ra / CD25 Reference Antibody (daclizumab)Anti-IL-2Ra/CD25 Reference Antibody (daclizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-3-sec-hplc.jpgAnti-IL-2Ra / CD25 Reference Antibody (daclizumab)The purity of Anti-IL-2Ra/CD25 Reference Antibody (daclizumab)is more than 99.49%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-3-od450.jpgAnti-IL-2Ra / CD25 Reference Antibody (daclizumab)Immobilized human IL 2Ralpha His at 2 &mug/mL can bind Anti-IL-2Ra/CD25 Reference Antibody (daclizumab) https://www.bosterbio.com/catalog/product/view/id/1282972026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-4-sds-page.jpgAnti-IL-2Ra / CD25 Reference Antibody (Inolimomab)Anti-IL-2Ra/CD25 Reference Antibody (Inolimomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-4-sec-hplc.jpgAnti-IL-2Ra / CD25 Reference Antibody (Inolimomab)The purity of Anti-IL-2Ra/CD25 Reference Antibody (Inolimomab)is more than 96.54% https://www.bosterbio.com/catalog/product/view/id/1282982026-03-10T04:38:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-5-sds-page.jpgAnti-IL-2Ra / CD25 Reference Antibody (camidanlumAb)Anti-IL-2Ra/CD25 Reference Antibody (camidanlumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00214-5-sec-hplc.jpgAnti-IL-2Ra / CD25 Reference Antibody (camidanlumAb)The purity of Anti-IL-2Ra/CD25 Reference Antibody (camidanlumAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1282992026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-1-sds-page.jpgAnti-AXL / UFO Reference Antibody (tilvestamab)Anti-AXL/UFO Reference Antibody (tilvestamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-1-sec-hplc.jpgAnti-AXL / UFO Reference Antibody (tilvestamab)The purity of Anti-AXL/UFO Reference Antibody (tilvestamab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-1-od450.jpgAnti-AXL / UFO Reference Antibody (tilvestamab)Immobilized human Axl FC at 2 &mug/mL can bind Anti-AXL/UFO Reference Antibody (tilvestamab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-1-facs.jpgAnti-AXL / UFO Reference Antibody (tilvestamab)Human AXL HEK293 cells were stained with Anti-AXL/UFO Reference Antibody (tilvestamab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-1-inhibition-of-cell-growth.jpgAnti-AXL / UFO Reference Antibody (tilvestamab)The endocytosis ratio tilvestamab by U251 increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-1-facs-1.jpgAnti-AXL / UFO Reference Antibody (tilvestamab)Anti-AXL/UFO Reference Antibody (tilvestamab) P-AKT Test was evaluated using U251 cell. The max induction fold was approximately 1.43. https://www.bosterbio.com/catalog/product/view/id/1283002026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-2-sds-page.jpgAnti-AXL / UFO Reference Antibody (enapotamab)Anti-AXL/UFO Reference Antibody (enapotamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-2-sec-hplc.jpgAnti-AXL / UFO Reference Antibody (enapotamab)The purity of Anti-AXL/UFO Reference Antibody (enapotamab)is more than 99.48%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-2-od450.jpgAnti-AXL / UFO Reference Antibody (enapotamab)Immobilized human Axl FC at 2 &mug/mL can bind Anti-AXL/UFO Reference Antibody (enapotamab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-2-facs.jpgAnti-AXL / UFO Reference Antibody (enapotamab)Human AXL HEK293 cells were stained with Anti-AXL/UFO Reference Antibody (enapotamab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1283012026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-3-sds-page.jpgAnti-AXL / UFO Reference Antibody (mipasetamAb)Anti-AXL/UFO Reference Antibody (mipasetamAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-3-sec-hplc.jpgAnti-AXL / UFO Reference Antibody (mipasetamAb)The purity of Anti-AXL/UFO Reference Antibody (mipasetamAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283022026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-4-sec-hplc.jpgAnti-AXL / UFO Reference Antibody (enapotamab vedotin)The purity of Anti-AXL/UFO Reference Antibody (enapotamab vedotin)is more than 99.9% https://www.bosterbio.com/catalog/product/view/id/1283032026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-5-sds-page.jpgAnti-AXL / UFO Reference Antibody (ORY012)Anti-AXL/UFO Reference Antibody (ORY012) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-5-sec-hplc.jpgAnti-AXL / UFO Reference Antibody (ORY012)The purity of Anti-AXL/UFO Reference Antibody (ORY012)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283042026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-6-sds-page.jpgAnti-AXL / UFO Reference Antibody (Tilvestamab-MMAE)Anti-AXL/UFO Reference Antibody (Tilvestamab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00226-6-sec-hplc.jpgAnti-AXL / UFO Reference Antibody (Tilvestamab-MMAE)The purity of Anti-AXL/UFO Reference Antibody (Tilvestamab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283052026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-4-sds-page.jpgAnti-FGFR2 / CD332 Reference Antibody (aprutumab)Anti-FGFR2/CD332 Reference Antibody (aprutumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-4-sec-hplc.jpgAnti-FGFR2 / CD332 Reference Antibody (aprutumab)The purity of Anti-FGFR2/CD332 Reference Antibody (aprutumab)is more than 98.69%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-4-facs.jpgAnti-FGFR2 / CD332 Reference Antibody (aprutumab)Human FGFR2-beta-IIIc (A13) CHOS cells were stained with Anti-FGFR2/CD332 Reference Antibody (aprutumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1283062026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-5-sds-page.jpgAnti-FGFR2 / CD332 Reference Antibody (bemarituzumab)Anti-FGFR2/CD332 Reference Antibody (bemarituzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-5-sec-hplc.jpgAnti-FGFR2 / CD332 Reference Antibody (bemarituzumab)The purity of Anti-FGFR2/CD332 Reference Antibody (bemarituzumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-5-facs.jpgAnti-FGFR2 / CD332 Reference Antibody (bemarituzumab)SNU-16 cells were stained with Anti-FGFR2/CD332 Reference Antibody (bemarituzumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-5-lysis.jpgAnti-FGFR2 / CD332 Reference Antibody (bemarituzumab)Anti-FGFR2/CD332 Reference Antibody (bemarituzumab) induced ADCC activity was evaluated using Human FGFR2 HEK293 Reporter Cell.The max induction fold was approximately 25.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-5-luminescence-intensity.jpgAnti-FGFR2 / CD332 Reference Antibody (bemarituzumab)Anti-FGFR2/CD332 Reference Antibody (bemarituzumab) -ADCC luciferase Assay on KATOIII cells. The maximum suppression factor is approximately 14.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00231-5-xenograft-snu-16-cell-model.jpgAnti-FGFR2 / CD332 Reference Antibody (bemarituzumab)Bemarituzumab inhibited the tumor growth of SNU-16 on Balb/c nude mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1283072026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00239-2-sds-page.jpgAnti-GPR49 / LGR5 Reference Antibody (BNC101)Anti-GPR49/LGR5 Reference Antibody (BNC101) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00239-2-sec-hplc.jpgAnti-GPR49 / LGR5 Reference Antibody (BNC101)The purity of Anti-GPR49/LGR5 Reference Antibody (BNC101)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283082026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00248-9-sds-page.jpgAnti-EMMPRIN / CD147 Reference Antibody (Centocor patent anti-CD147)Anti-EMMPRIN/CD147 Reference Antibody (Centocor patent anti-CD147) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00248-9-sec-hplc.jpgAnti-EMMPRIN / CD147 Reference Antibody (Centocor patent anti-CD147)The purity of Anti-EMMPRIN/CD147 Reference Antibody (Centocor patent anti-CD147)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283092026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00270-4-sds-page.jpgAnti-vWF Reference Antibody (Ajinomoto patent anti-vWF)Anti-vWF Reference Antibody (Ajinomoto patent anti-vWF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00270-4-sec-hplc.jpgAnti-vWF Reference Antibody (Ajinomoto patent anti-vWF)The purity of Anti-vWF Reference Antibody (Ajinomoto patent anti-vWF)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283102026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00270-5-sds-page.jpgAnti-vWF Reference Antibody (INSERM patent anti-vWF)Anti-vWF Reference Antibody (INSERM patent anti-vWF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00270-5-sec-hplc.jpgAnti-vWF Reference Antibody (INSERM patent anti-vWF)The purity of Anti-vWF Reference Antibody (INSERM patent anti-vWF)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283112026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-3-sds-page.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (adecatumumab)Anti-EpCAM/TROP1/CD326 Reference Antibody (adecatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-3-sec-hplc.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (adecatumumab)The purity of Anti-EpCAM/TROP1/CD326 Reference Antibody (adecatumumab)is more than 97.96% https://www.bosterbio.com/catalog/product/view/id/1283122026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-4-sds-page.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (citatuzumab)Anti-EpCAM/TROP1/CD326 Reference Antibody (citatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-4-sec-hplc.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (citatuzumab)The purity of Anti-EpCAM/TROP1/CD326 Reference Antibody (citatuzumab)is more than 97.95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-4-od450.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (citatuzumab)Immobilized human EpCAM/TROP1/CD326 https://www.bosterbio.com/catalog/product/view/id/1283132026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-5-sds-page.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (Tucotuzumab)Anti-EpCAM/TROP1/CD326 Reference Antibody (Tucotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-5-sec-hplc.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (Tucotuzumab)The purity of Anti-EpCAM/TROP1/CD326 Reference Antibody (Tucotuzumab)is more than 99.28% https://www.bosterbio.com/catalog/product/view/id/1283142026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-6-sds-page.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (oportuzumab)Anti-EpCAM/TROP1/CD326 Reference Antibody (oportuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00276-6-sec-hplc.jpgAnti-EpCAM / TROP1 / CD326 Reference Antibody (oportuzumab)The purity of Anti-EpCAM/TROP1/CD326 Reference Antibody (oportuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283152026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00278-2-sds-page.jpgAnti-CXCL10 / IP-10 Reference Antibody (eldelumab)Anti-CXCL10/IP-10 Reference Antibody (eldelumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00278-2-sec-hplc.jpgAnti-CXCL10 / IP-10 Reference Antibody (eldelumab)The purity of Anti-CXCL10/IP-10 Reference Antibody (eldelumab)is more than 99.28% https://www.bosterbio.com/catalog/product/view/id/1283162026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00278-3-sds-page.jpgAnti-CXCL10 / IP-10 Reference Antibody (NI-0801)Anti-CXCL10/IP-10 Reference Antibody (NI-0801) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00278-3-sec-hplc.jpgAnti-CXCL10 / IP-10 Reference Antibody (NI-0801)The purity of Anti-CXCL10/IP-10 Reference Antibody (NI-0801)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283172026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00281-1-sds-page.jpgAnti-CSF3R / G-CSFR Reference Antibody (CSL patent anti-G-CSFR)Anti-CSF3R/G-CSFR Reference Antibody (CSL patent anti-G-CSFR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00281-1-sec-hplc.jpgAnti-CSF3R / G-CSFR Reference Antibody (CSL patent anti-G-CSFR)The purity of Anti-CSF3R/G-CSFR Reference Antibody (CSL patent anti-G-CSFR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283182026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-2-sds-page.jpgAnti-ICOS / CD278 Reference Antibody (feladilimab)Anti-ICOS/CD278 Reference Antibody (feladilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-2-sec-hplc.jpgAnti-ICOS / CD278 Reference Antibody (feladilimab)The purity of Anti-ICOS/CD278 Reference Antibody (feladilimab)is more than 99.12%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-2-od450.jpgAnti-ICOS / CD278 Reference Antibody (feladilimab)Immobilized human ICOS FC at 2 &mug/mL can bind Anti-ICOS/CD278 Reference Antibody (feladilimab) https://www.bosterbio.com/catalog/product/view/id/1283192026-03-10T04:38:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-3-sds-page.jpgAnti-ICOS / CD278 Reference Antibody (vopratelimab)Anti-ICOS/CD278 Reference Antibody (vopratelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-3-sec-hplc.jpgAnti-ICOS / CD278 Reference Antibody (vopratelimab)The purity of Anti-ICOS/CD278 Reference Antibody (vopratelimab)is more than 99.09% https://www.bosterbio.com/catalog/product/view/id/1283202026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-4-sds-page.jpgAnti-ICOS / CD278 Reference Antibody (MEDI-570)Anti-ICOS/CD278 Reference Antibody (MEDI-570) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-4-sec-hplc.jpgAnti-ICOS / CD278 Reference Antibody (MEDI-570)The purity of Anti-ICOS/CD278 Reference Antibody (MEDI-570)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283212026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-5-sds-page.jpgAnti-ICOS / CD278 Reference Antibody (alomfilimab)Anti-ICOS/CD278 Reference Antibody (alomfilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00291-5-sec-hplc.jpgAnti-ICOS / CD278 Reference Antibody (alomfilimab)The purity of Anti-ICOS/CD278 Reference Antibody (alomfilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283222026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00293-2-sds-page.jpgAnti-c-RET Reference Antibody (Regeneron patent anti-RET)Anti-c-RET Reference Antibody (Regeneron patent anti-RET) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00293-2-sec-hplc.jpgAnti-c-RET Reference Antibody (Regeneron patent anti-RET)The purity of Anti-c-RET Reference Antibody (Regeneron patent anti-RET)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283232026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00295-1-sds-page.jpgAnti-CXCR3 / GPR9 / CD183 Reference Antibody (Genzyme patent anti-CXCR3)Anti-CXCR3/GPR9/CD183 Reference Antibody (Genzyme patent anti-CXCR3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00295-1-sec-hplc.jpgAnti-CXCR3 / GPR9 / CD183 Reference Antibody (Genzyme patent anti-CXCR3)The purity of Anti-CXCR3/GPR9/CD183 Reference Antibody (Genzyme patent anti-CXCR3)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00295-1-od450.jpgAnti-CXCR3 / GPR9 / CD183 Reference Antibody (Genzyme patent anti-CXCR3)Immobilized human CXCR3 VLP Protein at 8 &mug/mL can bind Anti-CXCR3/GPR9/CD183 Reference Antibody (Genzyme patent anti-CXCR3) https://www.bosterbio.com/catalog/product/view/id/1283242026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-4-sds-page.jpgAnti-IFNAR1 Reference Antibody (anifrolumab)Anti-IFNAR1 Reference Antibody (anifrolumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-4-sec-hplc.jpgAnti-IFNAR1 Reference Antibody (anifrolumab)The purity of Anti-IFNAR1 Reference Antibody (anifrolumab)is more than 98.75%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-4-od450.jpgAnti-IFNAR1 Reference Antibody (anifrolumab)Immobilized human IFNAR1 https://www.bosterbio.com/catalog/product/view/id/1283252026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-5-sds-page.jpgAnti-IFNAR1 Reference Antibody (Medarex patent anti-IFNAR-1)Anti-IFNAR1 Reference Antibody (Medarex patent anti-IFNAR-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-5-sec-hplc.jpgAnti-IFNAR1 Reference Antibody (Medarex patent anti-IFNAR-1)The purity of Anti-IFNAR1 Reference Antibody (Medarex patent anti-IFNAR-1)is more than 98.75%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-5-od450.jpgAnti-IFNAR1 Reference Antibody (Medarex patent anti-IFNAR-1)Immobilized human IFNAR1 https://www.bosterbio.com/catalog/product/view/id/1283262026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-6-sds-page.jpgAnti-IFNAR1 Reference Antibody (Faralimomab)Anti-IFNAR1 Reference Antibody (Faralimomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00306-6-sec-hplc.jpgAnti-IFNAR1 Reference Antibody (Faralimomab)The purity of Anti-IFNAR1 Reference Antibody (Faralimomab)is more than 99.35% https://www.bosterbio.com/catalog/product/view/id/1283272026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00322-1-sds-page.jpgAnti-BACE1 Reference Antibody (Genentech anti-BACE1)Anti-BACE1 Reference Antibody (Genentech anti-BACE1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00322-1-sec-hplc.jpgAnti-BACE1 Reference Antibody (Genentech anti-BACE1)The purity of Anti-BACE1 Reference Antibody (Genentech anti-BACE1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283282026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00335-2-sds-page.jpgAnti-IGF-2 Reference Antibody (DX-2647)Anti-IGF-2 Reference Antibody (DX-2647) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00335-2-sec-hplc.jpgAnti-IGF-2 Reference Antibody (DX-2647)The purity of Anti-IGF-2 Reference Antibody (DX-2647)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283292026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-1-sds-page.jpgAnti-NGF / bNGF Reference Antibody (Frunevetmab)Anti-NGF/bNGF Reference Antibody (Frunevetmab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-1-sec-hplc.jpgAnti-NGF / bNGF Reference Antibody (Frunevetmab)The purity of Anti-NGF/bNGF Reference Antibody (Frunevetmab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283302026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-2-sds-page.jpgAnti-NGF / bNGF Reference Antibody (tanezumab)Anti-NGF/bNGF Reference Antibody (tanezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-2-sec-hplc.jpgAnti-NGF / bNGF Reference Antibody (tanezumab)The purity of Anti-NGF/bNGF Reference Antibody (tanezumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283312026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-3-sds-page.jpgAnti-NGF / bNGF Reference Antibody (fasinumab)Anti-NGF/bNGF Reference Antibody (fasinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-3-sec-hplc.jpgAnti-NGF / bNGF Reference Antibody (fasinumab)The purity of Anti-NGF/bNGF Reference Antibody (fasinumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283322026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-4-sds-page.jpgAnti-NGF / bNGF Reference Antibody (MEDI-578)Anti-NGF/bNGF Reference Antibody (MEDI-578) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-4-sec-hplc.jpgAnti-NGF / bNGF Reference Antibody (MEDI-578)The purity of Anti-NGF/bNGF Reference Antibody (MEDI-578)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283332026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-5-sds-page.jpgAnti-NGF / bNGF Reference Antibody (fulranumab)Anti-NGF/bNGF Reference Antibody (fulranumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-5-sec-hplc.jpgAnti-NGF / bNGF Reference Antibody (fulranumab)The purity of Anti-NGF/bNGF Reference Antibody (fulranumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283342026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-6-sds-page.jpgAnti-NGF / bNGF Reference Antibody (AS2886401-00)Anti-NGF/bNGF Reference Antibody (AS2886401-00) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-6-sec-hplc.jpgAnti-NGF / bNGF Reference Antibody (AS2886401-00)The purity of Anti-NGF/bNGF Reference Antibody (AS2886401-00)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283352026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-7-sds-page.jpgAnti-NGF / bNGF Reference Antibody (Izenivetmab)Anti-NGF/bNGF Reference Antibody (Izenivetmab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00341-7-sec-hplc.jpgAnti-NGF / bNGF Reference Antibody (Izenivetmab)The purity of Anti-NGF/bNGF Reference Antibody (Izenivetmab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283362026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-3-sds-page.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (tisotumab)Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (tisotumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-3-sec-hplc.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (tisotumab)The purity of Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (tisotumab)is more than 99.08% https://www.bosterbio.com/catalog/product/view/id/1283372026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-4-sds-page.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (TNX-832)Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (TNX-832) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-4-sec-hplc.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (TNX-832)The purity of Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (TNX-832)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283382026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-5-sds-page.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (Chugai patent anti-TF)Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (Chugai patent anti-TF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-5-sec-hplc.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (Chugai patent anti-TF)The purity of Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (Chugai patent anti-TF)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283392026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-6-sds-page.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (tisotumab vedotin)Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (tisotumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00342-6-sec-hplc.jpgAnti-F3 / Factor III / Tissue Factor / CD142 Reference Antibody (tisotumab vedotin)The purity of Anti-F3/Factor III/Tissue Factor/CD142 Reference Antibody (tisotumab vedotin)is more than 99.08% https://www.bosterbio.com/catalog/product/view/id/1283402026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-5-sds-page.jpgAnti-CD4 Reference Antibody (ibalizumab)Anti-CD4 Reference Antibody (ibalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-5-sec-hplc.jpgAnti-CD4 Reference Antibody (ibalizumab)The purity of Anti-CD4 Reference Antibody (ibalizumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-5-facs.jpgAnti-CD4 Reference Antibody (ibalizumab)Human CD4 CHO cells were stained with Anti-CD4 Reference Antibody (ibalizumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-5-luminescence-intensity.jpgAnti-CD4 Reference Antibody (ibalizumab)Anti-CD4 Reference Antibody (ibalizumab) Pseudoviral inhibition was evaluated using Tzmbl.The IC50 was approximately 0.441 nM. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-5-od450.jpgAnti-CD4 Reference Antibody (ibalizumab)Anti-CD4 Reference Antibody (ibalizumab)Activation inhibition was evaluated using PBMC. The max induction fold was approximately 1.71 https://www.bosterbio.com/catalog/product/view/id/1283412026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-6-sds-page.jpgAnti-CD4 Reference Antibody (Semzuvolimab)Anti-CD4 Reference Antibody (Semzuvolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-6-sec-hplc.jpgAnti-CD4 Reference Antibody (Semzuvolimab)The purity of Anti-CD4 Reference Antibody (Semzuvolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283422026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-7-sds-page.jpgAnti-CD4 Reference Antibody (tregalizumab)Anti-CD4 Reference Antibody (tregalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-7-sec-hplc.jpgAnti-CD4 Reference Antibody (tregalizumab)The purity of Anti-CD4 Reference Antibody (tregalizumab)is more than 98.97% https://www.bosterbio.com/catalog/product/view/id/1283432026-03-10T04:38:56+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-8-sds-page.jpgAnti-CD4 Reference Antibody (TRX1)Anti-CD4 Reference Antibody (TRX1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00344-8-sec-hplc.jpgAnti-CD4 Reference Antibody (TRX1)The purity of Anti-CD4 Reference Antibody (TRX1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283442026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00348-1-sds-page.jpgAnti-PDGFB Reference Antibody (MOR-8457)Anti-PDGFB Reference Antibody (MOR-8457) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00348-1-sec-hplc.jpgAnti-PDGFB Reference Antibody (MOR-8457)The purity of Anti-PDGFB Reference Antibody (MOR-8457)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283452026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00350-2-sds-page.jpgAnti-LEPR / CD295 Reference Antibody (mibavademab)Anti-LEPR/CD295 Reference Antibody (mibavademab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00350-2-sec-hplc.jpgAnti-LEPR / CD295 Reference Antibody (mibavademab)The purity of Anti-LEPR/CD295 Reference Antibody (mibavademab)is more than 98.36% https://www.bosterbio.com/catalog/product/view/id/1283462026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-sds-page.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (labetuzumab)Anti-CEACAM5/CEA/CD66e Reference Antibody (labetuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-sec-hplc.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (labetuzumab)The purity of Anti-CEACAM5/CEA/CD66e Reference Antibody (labetuzumab)is more than 98.53%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-od450.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (labetuzumab)Immobilized human CEACAM5 His Biotin at 2 &mug/mL can bind Anti-CEACAM5/CEA/CD66e Reference Antibody (labetuzumab) https://www.bosterbio.com/catalog/product/view/id/1283472026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-5-sds-page.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab)Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-5-sec-hplc.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab)The purity of Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab)is more than 95.93%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-5-od450.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab)Immobilized human CEACAM5 His at 2 &mug/mL can bind Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab) https://www.bosterbio.com/catalog/product/view/id/1283482026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-6-sds-page.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab-MMAE)Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-6-sec-hplc.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab-MMAE)The purity of Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab-MMAE)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-6-od450.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab-MMAE)Immobilized human CEACAM5 His at 2 &mug/mL can bind Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab-MMAE) https://www.bosterbio.com/catalog/product/view/id/1283492026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-7-sds-page.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (cergutuzumAb)Anti-CEACAM5/CEA/CD66e Reference Antibody (cergutuzumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-7-sec-hplc.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (cergutuzumAb)The purity of Anti-CEACAM5/CEA/CD66e Reference Antibody (cergutuzumAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283502026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-8-sds-page.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (Immunomedics patent anti-CEACAM5 (Class III))Anti-CEACAM5/CEA/CD66e Reference Antibody (Immunomedics patent anti-CEACAM5 (Class III)) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-8-sec-hplc.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (Immunomedics patent anti-CEACAM5 (Class III))The purity of Anti-CEACAM5/CEA/CD66e Reference Antibody (Immunomedics patent anti-CEACAM5 (Class III))is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283512026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-9-sds-page.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (labetuzumab govitecan)Anti-CEACAM5/CEA/CD66e Reference Antibody (labetuzumab govitecan) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-9-sec-hplc.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (labetuzumab govitecan)The purity of Anti-CEACAM5/CEA/CD66e Reference Antibody (labetuzumab govitecan)is more than 98.53% https://www.bosterbio.com/catalog/product/view/id/1283522026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-10-sds-page.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab ravtansine)Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab ravtansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00356-10-sec-hplc.jpgAnti-CEACAM5 / CEA / CD66e Reference Antibody (tusamitamab ravtansine)The purity of Anti-CEACAM5/CEA/CD66e Reference Antibody (tusamitamab ravtansine)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283532026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-3-sds-page.jpgAnti-CD47 Reference Antibody (lemzoparlimab)Anti-CD47 Reference Antibody (lemzoparlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-3-sec-hplc.jpgAnti-CD47 Reference Antibody (lemzoparlimab)The purity of Anti-CD47 Reference Antibody (lemzoparlimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-3-od450.jpgAnti-CD47 Reference Antibody (lemzoparlimab)Immobilized Recomvinant human CD47(c His) at1.5 &mug/mL can bind Anti-CD47 Reference Antibody (lemzoparlimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-3-facs.jpgAnti-CD47 Reference Antibody (lemzoparlimab)PANC-1 cells were stained with Anti-CD47 Reference Antibody (lemzoparlimab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-3-facs-1.jpgAnti-CD47 Reference Antibody (lemzoparlimab)Anti-CD47 Reference Antibody (lemzoparlimab) FACS Blocking was evaluated using CCRF-CEM. The IC50 was approximately 0.4557 ug/mL.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-3-phagocytosis.jpgAnti-CD47 Reference Antibody (lemzoparlimab)The phagocytosis ratio lemzoparlimab by CCRF-CEM increased with the increase of antibody concentration https://www.bosterbio.com/catalog/product/view/id/1283542026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-4-sds-page.jpgAnti-CD47 Reference Antibody (letaplimab)Anti-CD47 Reference Antibody (letaplimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-4-sec-hplc.jpgAnti-CD47 Reference Antibody (letaplimab)The purity of Anti-CD47 Reference Antibody (letaplimab)is more than 99.55% https://www.bosterbio.com/catalog/product/view/id/1283552026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-5-sds-page.jpgAnti-CD47 Reference Antibody (CC-90002)Anti-CD47 Reference Antibody (CC-90002) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-5-sec-hplc.jpgAnti-CD47 Reference Antibody (CC-90002)The purity of Anti-CD47 Reference Antibody (CC-90002)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283562026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-6-sds-page.jpgAnti-CD47 Reference Antibody (ligufalimab)Anti-CD47 Reference Antibody (ligufalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-6-sec-hplc.jpgAnti-CD47 Reference Antibody (ligufalimab)The purity of Anti-CD47 Reference Antibody (ligufalimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283572026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-7-sds-page.jpgAnti-CD47 Reference Antibody (magrolimab)Anti-CD47 Reference Antibody (magrolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-7-sec-hplc.jpgAnti-CD47 Reference Antibody (magrolimab)The purity of Anti-CD47 Reference Antibody (magrolimab)is more than 98.18%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-7-xenograft-raji-cell-model.jpgAnti-CD47 Reference Antibody (magrolimab)Magrolimab inhibited the tumor growth of Raji on NOD.SCID mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1283582026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-8-sds-page.jpgAnti-CD47 Reference Antibody (urabrelimab)Anti-CD47 Reference Antibody (urabrelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00360-8-sec-hplc.jpgAnti-CD47 Reference Antibody (urabrelimab)The purity of Anti-CD47 Reference Antibody (urabrelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283592026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00363-2-sds-page.jpgAnti-TNFSF11 / RANKL / CD254 Reference Antibody (denosumab)Anti-TNFSF11/RANKL/CD254 Reference Antibody (denosumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00363-2-sec-hplc.jpgAnti-TNFSF11 / RANKL / CD254 Reference Antibody (denosumab)The purity of Anti-TNFSF11/RANKL/CD254 Reference Antibody (denosumab)is more than 97.25% https://www.bosterbio.com/catalog/product/view/id/1283602026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00366-4-sds-page.jpgAnti-PDGFRA / CD140a Reference Antibody (olaratumab)Anti-PDGFRA/CD140a Reference Antibody (olaratumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00366-4-sec-hplc.jpgAnti-PDGFRA / CD140a Reference Antibody (olaratumab)The purity of Anti-PDGFRA/CD140a Reference Antibody (olaratumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00366-4-od450.jpgAnti-PDGFRA / CD140a Reference Antibody (olaratumab)Immobilized human PDGFRA/CD140a https://www.bosterbio.com/catalog/product/view/id/1283612026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00366-5-sds-page.jpgAnti-PDGFRA / CD140a Reference Antibody (tovetumab)Anti-PDGFRA/CD140a Reference Antibody (tovetumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00366-5-sec-hplc.jpgAnti-PDGFRA / CD140a Reference Antibody (tovetumab)The purity of Anti-PDGFRA/CD140a Reference Antibody (tovetumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283622026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00367-1-sds-page.jpgAnti-F8 / Factor VIII Reference Antibody (Novo Nordisk patent anti-Factor VIII)Anti-F8/Factor VIII Reference Antibody (Novo Nordisk patent anti-Factor VIII) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00367-1-sec-hplc.jpgAnti-F8 / Factor VIII Reference Antibody (Novo Nordisk patent anti-Factor VIII)The purity of Anti-F8/Factor VIII Reference Antibody (Novo Nordisk patent anti-Factor VIII)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283632026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00370-2-sds-page.jpgAnti-ANGPT2 Reference Antibody (nesvacumab)Anti-ANGPT2 Reference Antibody (nesvacumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00370-2-sec-hplc.jpgAnti-ANGPT2 Reference Antibody (nesvacumab)The purity of Anti-ANGPT2 Reference Antibody (nesvacumab)is more than 99.11%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00370-2-od450.jpgAnti-ANGPT2 Reference Antibody (nesvacumab)Immobilized human ANGPT2 His at 2 &mug/mL can bind Anti-ANGPT2 Reference Antibody (nesvacumab) https://www.bosterbio.com/catalog/product/view/id/1283642026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00370-3-sds-page.jpgAnti-ANGPT2 Reference Antibody (zansecimab)Anti-ANGPT2 Reference Antibody (zansecimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00370-3-sec-hplc.jpgAnti-ANGPT2 Reference Antibody (zansecimab)The purity of Anti-ANGPT2 Reference Antibody (zansecimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283652026-03-10T04:38:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00370-4-sds-page.jpgAnti-ANGPT2 Reference Antibody (MEDI3617)Anti-ANGPT2 Reference Antibody (MEDI3617) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00370-4-sec-hplc.jpgAnti-ANGPT2 Reference Antibody (MEDI3617)The purity of Anti-ANGPT2 Reference Antibody (MEDI3617)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283662026-03-10T04:38:57+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1283672026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00376-1-sds-page.jpgAnti-TLR7 Reference Antibody (U.Tokyo patent anti-TLR7)Anti-TLR7 Reference Antibody (U.Tokyo patent anti-TLR7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00376-1-sec-hplc.jpgAnti-TLR7 Reference Antibody (U.Tokyo patent anti-TLR7)The purity of Anti-TLR7 Reference Antibody (U.Tokyo patent anti-TLR7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283682026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00377-4-sds-page.jpgAnti-CD46 Reference Antibody (FOR46)Anti-CD46 Reference Antibody (FOR46) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00377-4-sec-hplc.jpgAnti-CD46 Reference Antibody (FOR46)The purity of Anti-CD46 Reference Antibody (FOR46)is more than 98.24% https://www.bosterbio.com/catalog/product/view/id/1283692026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00390-2-sds-page.jpgAnti-CCR7 / CD197 Reference Antibody (R707)Anti-CCR7/CD197 Reference Antibody (R707) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00390-2-sec-hplc.jpgAnti-CCR7 / CD197 Reference Antibody (R707)The purity of Anti-CCR7/CD197 Reference Antibody (R707)is more than 99.08% https://www.bosterbio.com/catalog/product/view/id/1283702026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-7-sds-page.jpgAnti-IFNg Reference Antibody (fontolizumab)Anti-IFNg Reference Antibody (fontolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-7-sec-hplc.jpgAnti-IFNg Reference Antibody (fontolizumab)The purity of Anti-IFNg Reference Antibody (fontolizumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-7-od450.jpgAnti-IFNg Reference Antibody (fontolizumab)Immobilized human IFN 污 His at 2 &mug/mL can bind Anti-IFNg Reference Antibody (fontolizumab) https://www.bosterbio.com/catalog/product/view/id/1283712026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-8-sds-page.jpgAnti-IFNg Reference Antibody (AMG 811)Anti-IFNg Reference Antibody (AMG 811) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-8-sec-hplc.jpgAnti-IFNg Reference Antibody (AMG 811)The purity of Anti-IFNg Reference Antibody (AMG 811)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-8-od450.jpgAnti-IFNg Reference Antibody (AMG 811)Immobilized human IFN 污 His at4 &mug/mL can bind Anti-IFNg Reference Antibody (AMG 811) https://www.bosterbio.com/catalog/product/view/id/1283722026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-9-sds-page.jpgAnti-IFNg Reference Antibody (emapalumab)Anti-IFNg Reference Antibody (emapalumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00393-9-sec-hplc.jpgAnti-IFNg Reference Antibody (emapalumab)The purity of Anti-IFNg Reference Antibody (emapalumab)is more than 99% https://www.bosterbio.com/catalog/product/view/id/1283732026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-3-sds-page.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (conatumumab)Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (conatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-3-sec-hplc.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (conatumumab)The purity of Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (conatumumab)is more than 98.9%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-3-od450.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (conatumumab)Immobilized Cyno DR5 His at 2 &mug/mL can bind Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (conatumumab) https://www.bosterbio.com/catalog/product/view/id/1283742026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-8-sds-page.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (lexatumumab)Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (lexatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-8-sec-hplc.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (lexatumumab)The purity of Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (lexatumumab)is more than 99.04%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-8-od450.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (lexatumumab)Immobilized human TNFRSF10B/TRAILR2/CD262 https://www.bosterbio.com/catalog/product/view/id/1283752026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-5-sds-page.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (benufutamab)Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (benufutamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-5-sec-hplc.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (benufutamab)The purity of Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (benufutamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283762026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-6-sds-page.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (tigatuzumab)Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (tigatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-6-sec-hplc.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (tigatuzumab)The purity of Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (tigatuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283772026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-7-sds-page.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (tilogotamab)Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (tilogotamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-7-sec-hplc.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (tilogotamab)The purity of Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (tilogotamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283782026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-4-sds-page.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (drozitumab)Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (drozitumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-4-sec-hplc.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (drozitumab)The purity of Anti-TNFRSF10B/TRAILR2/CD262 Reference Antibody (drozitumab)is more than 99.68%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00410-4-od450.jpgAnti-TNFRSF10B / TRAILR2 / CD262 Reference Antibody (drozitumab)Immobilized Cynomolgus TRAIL R2/DR5/ TNFRSF10B Protein https://www.bosterbio.com/catalog/product/view/id/1283792026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00411-1-sds-page.jpgAnti-MIF Reference Antibody (imalumab)Anti-MIF Reference Antibody (imalumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00411-1-sec-hplc.jpgAnti-MIF Reference Antibody (imalumab)The purity of Anti-MIF Reference Antibody (imalumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283802026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-3-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (secukinumab)Anti-CTLA-8/IL-17a Reference Antibody (secukinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-3-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (secukinumab)The purity of Anti-CTLA-8/IL-17a Reference Antibody (secukinumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-3-od450.jpgAnti-CTLA-8 / IL-17a Reference Antibody (secukinumab)Immobilized human IL 17A FC at 2 &mug/mL can bind Anti-CTLA-8/IL-17a Reference Antibody (secukinumab) https://www.bosterbio.com/catalog/product/view/id/1283812026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-4-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (vunakizumab)Anti-CTLA-8/IL-17a Reference Antibody (vunakizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-4-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (vunakizumab)The purity of Anti-CTLA-8/IL-17a Reference Antibody (vunakizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283822026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-5-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (perakizumab)Anti-CTLA-8/IL-17a Reference Antibody (perakizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-5-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (perakizumab)The purity of Anti-CTLA-8/IL-17a Reference Antibody (perakizumab)is more than 93.74% https://www.bosterbio.com/catalog/product/view/id/1283832026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-6-sds-page.jpgAnti-CTLA-8 / IL-17a Antibody (SY18-VHH-11)Anti-CTLA-8/IL-17a Antibody (SY18-VHH-11) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-6-sec-hplc.jpgAnti-CTLA-8 / IL-17a Antibody (SY18-VHH-11)The purity of Anti-CTLA-8/IL-17a Antibody (SY18-VHH-11)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283842026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-7-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (CAT-2200)Anti-CTLA-8/IL-17a Reference Antibody (CAT-2200) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-7-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (CAT-2200)The purity of Anti-CTLA-8/IL-17a Reference Antibody (CAT-2200)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283852026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-8-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (ixekizumab)Anti-CTLA-8/IL-17a Reference Antibody (ixekizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-8-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (ixekizumab)The purity of Anti-CTLA-8/IL-17a Reference Antibody (ixekizumab)is more than 98.86% https://www.bosterbio.com/catalog/product/view/id/1283862026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-9-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (netakimab)Anti-CTLA-8/IL-17a Reference Antibody (netakimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-9-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (netakimab)The purity of Anti-CTLA-8/IL-17a Reference Antibody (netakimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283872026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-10-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (UCB patent anti-IL-17)Anti-CTLA-8/IL-17a Reference Antibody (UCB patent anti-IL-17) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-10-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (UCB patent anti-IL-17)The purity of Anti-CTLA-8/IL-17a Reference Antibody (UCB patent anti-IL-17)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283882026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-11-sds-page.jpgAnti-CTLA-8 / IL-17a Reference Antibody (Xeligekimab)Anti-CTLA-8/IL-17a Reference Antibody (Xeligekimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00421-11-sec-hplc.jpgAnti-CTLA-8 / IL-17a Reference Antibody (Xeligekimab)The purity of Anti-CTLA-8/IL-17a Reference Antibody (Xeligekimab)is more than 99.48% https://www.bosterbio.com/catalog/product/view/id/1283892026-03-10T04:38:58+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-1-sds-page.jpgAnti-FAP Reference Antibody (sibrotuzumab)Anti-FAP Reference Antibody (sibrotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-1-sec-hplc.jpgAnti-FAP Reference Antibody (sibrotuzumab)The purity of Anti-FAP Reference Antibody (sibrotuzumab)is more than 98.9%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00422-1-od450.jpgAnti-FAP Reference Antibody (sibrotuzumab)Immobilized human FAP His at 2 &mug/mL can bind Anti-FAP Reference Antibody (sibrotuzumab) https://www.bosterbio.com/catalog/product/view/id/1283902026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00423-2-sds-page.jpgAnti-CXCL8 / IL-8 Reference Antibody (HuMax-IL8)Anti-CXCL8/IL-8 Reference Antibody (HuMax-IL8) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 91.8%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00423-2-sec-hplc.jpgAnti-CXCL8 / IL-8 Reference Antibody (HuMax-IL8)The purity of Anti-CXCL8/IL-8 Reference Antibody (HuMax-IL8)is more than 91.32%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00423-2-od450.jpgAnti-CXCL8 / IL-8 Reference Antibody (HuMax-IL8)Immobilized human IL 8 His at 2 &mug/mL can bind Anti-CXCL8/IL-8 Reference Antibody (HuMax-IL8) https://www.bosterbio.com/catalog/product/view/id/1283912026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00423-3-sds-page.jpgAnti-CXCL8 / IL-8 Reference Antibody (ABX-IL8)Anti-CXCL8/IL-8 Reference Antibody (ABX-IL8) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00423-3-sec-hplc.jpgAnti-CXCL8 / IL-8 Reference Antibody (ABX-IL8)The purity of Anti-CXCL8/IL-8 Reference Antibody (ABX-IL8)is more than 98.07% https://www.bosterbio.com/catalog/product/view/id/1283922026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00423-4-sds-page.jpgAnti-CXCL8 / IL-8 Reference Antibody (Genentech patent anti-IL-8)Anti-CXCL8/IL-8 Reference Antibody (Genentech patent anti-IL-8) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00423-4-sec-hplc.jpgAnti-CXCL8 / IL-8 Reference Antibody (Genentech patent anti-IL-8)The purity of Anti-CXCL8/IL-8 Reference Antibody (Genentech patent anti-IL-8)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283932026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00427-1-sds-page.jpgAnti-EPOR Reference Antibody (Abbott patent anti-EPO Receptor)Anti-EPOR Reference Antibody (Abbott patent anti-EPO Receptor) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00427-1-sec-hplc.jpgAnti-EPOR Reference Antibody (Abbott patent anti-EPO Receptor)The purity of Anti-EPOR Reference Antibody (Abbott patent anti-EPO Receptor)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283942026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00459-sds-page.jpgAnti-IL-21 Reference Antibody (avizakimab)Anti-IL-21 Reference Antibody (avizakimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00459-sec-hplc.jpgAnti-IL-21 Reference Antibody (avizakimab)The purity of Anti-IL-21 Reference Antibody (avizakimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283952026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00459-1-sds-page.jpgAnti-IL-21 Reference Antibody (Lilly patent anti-IL-21)Anti-IL-21 Reference Antibody (Lilly patent anti-IL-21) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00459-1-sec-hplc.jpgAnti-IL-21 Reference Antibody (Lilly patent anti-IL-21)The purity of Anti-IL-21 Reference Antibody (Lilly patent anti-IL-21)is more than 99.35% https://www.bosterbio.com/catalog/product/view/id/1283962026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-5-sds-page.jpgAnti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (etrolizumab)Anti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (etrolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-5-sec-hplc.jpgAnti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (etrolizumab)The purity of Anti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (etrolizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1283972026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-4-sds-page.jpgAnti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (abrilumab)Anti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (abrilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00468-4-sec-hplc.jpgAnti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (abrilumab)The purity of Anti-Integrin a4b7 (ITGA4 & ITGB7) Reference Antibody (abrilumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283982026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00478-sds-page.jpgAnti-FGF23 Reference Antibody (burosumab)Anti-FGF23 Reference Antibody (burosumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00478-sec-hplc.jpgAnti-FGF23 Reference Antibody (burosumab)The purity of Anti-FGF23 Reference Antibody (burosumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1283992026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00480-6-sds-page.jpgAnti-CD5 Reference Antibody (Magenta patent anti-CD5)Anti-CD5 Reference Antibody (Magenta patent anti-CD5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00480-6-sec-hplc.jpgAnti-CD5 Reference Antibody (Magenta patent anti-CD5)The purity of Anti-CD5 Reference Antibody (Magenta patent anti-CD5)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284002026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00483-1-sds-page.jpgAnti-MPL / TPOR / CD110 Reference Antibody (TA136)Anti-MPL/TPOR/CD110 Reference Antibody (TA136) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00483-1-sec-hplc.jpgAnti-MPL / TPOR / CD110 Reference Antibody (TA136)The purity of Anti-MPL/TPOR/CD110 Reference Antibody (TA136)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284012026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00485-sds-page.jpgAnti-NOTCH3 Reference Antibody (tarextumab)Anti-NOTCH3 Reference Antibody (tarextumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00485-sec-hplc.jpgAnti-NOTCH3 Reference Antibody (tarextumab)The purity of Anti-NOTCH3 Reference Antibody (tarextumab)is more than 99.3% https://www.bosterbio.com/catalog/product/view/id/1284022026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00485-1-sds-page.jpgAnti-NOTCH3 Reference Antibody (Genentech patent anti-Notch3)Anti-NOTCH3 Reference Antibody (Genentech patent anti-Notch3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00485-1-sec-hplc.jpgAnti-NOTCH3 Reference Antibody (Genentech patent anti-Notch3)The purity of Anti-NOTCH3 Reference Antibody (Genentech patent anti-Notch3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284032026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00489-2-sds-page.jpgAnti-MER / MERTK Reference Antibody (RGX-019)Anti-MER/MERTK Reference Antibody (RGX-019) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00489-2-sec-hplc.jpgAnti-MER / MERTK Reference Antibody (RGX-019)The purity of Anti-MER/MERTK Reference Antibody (RGX-019)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284042026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00492-sds-page.jpgAnti-IL-1RL1 / ST2 / IL-33R Reference Antibody (melrilimab)Anti-IL-1RL1/ST2/IL-33R Reference Antibody (melrilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00492-sec-hplc.jpgAnti-IL-1RL1 / ST2 / IL-33R Reference Antibody (melrilimab)The purity of Anti-IL-1RL1/ST2/IL-33R Reference Antibody (melrilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284052026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00492-1-sds-page.jpgAnti-IL-1RL1 / ST2 / IL-33R Reference Antibody (astegolimab)Anti-IL-1RL1/ST2/IL-33R Reference Antibody (astegolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00492-1-sec-hplc.jpgAnti-IL-1RL1 / ST2 / IL-33R Reference Antibody (astegolimab)The purity of Anti-IL-1RL1/ST2/IL-33R Reference Antibody (astegolimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284062026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00513-1-sds-page.jpgAnti-DLK1 Reference Antibody (LIV-1205)Anti-DLK1 Reference Antibody (LIV-1205) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00513-1-sec-hplc.jpgAnti-DLK1 Reference Antibody (LIV-1205)The purity of Anti-DLK1 Reference Antibody (LIV-1205)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00513-1-od450.jpgAnti-DLK1 Reference Antibody (LIV-1205)Immobilized human DLK1.1 His at 2 &mug/mL can bind Anti-DLK1 Reference Antibody (LIV-1205)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00513-1-facs.jpgAnti-DLK1 Reference Antibody (LIV-1205)Human DLK1 HEK293 cells were stained with Anti-DLK1 Reference Antibody (LIV-1205) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1284072026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00529-2-sds-page.jpgAnti-CD69 Reference Antibody (Genefrontier patent anti-CD69)Anti-CD69 Reference Antibody (Genefrontier patent anti-CD69) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00529-2-sec-hplc.jpgAnti-CD69 Reference Antibody (Genefrontier patent anti-CD69)The purity of Anti-CD69 Reference Antibody (Genefrontier patent anti-CD69)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284082026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-3-sds-page.jpgAnti-VEGFR1 / FLT1 Reference Antibody (icrucumab)Anti-VEGFR1/FLT1 Reference Antibody (icrucumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-3-sec-hplc.jpgAnti-VEGFR1 / FLT1 Reference Antibody (icrucumab)The purity of Anti-VEGFR1/FLT1 Reference Antibody (icrucumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284092026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-4-sds-page.jpgAnti-VEGFR1 / FLT1 Reference Antibody (Abbott patent anti-Flt1)Anti-VEGFR1/FLT1 Reference Antibody (Abbott patent anti-Flt1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00534-4-sec-hplc.jpgAnti-VEGFR1 / FLT1 Reference Antibody (Abbott patent anti-Flt1)The purity of Anti-VEGFR1/FLT1 Reference Antibody (Abbott patent anti-Flt1)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284102026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00537-1-sds-page.jpgAnti-F9 / Factor IX Reference Antibody (emicizumab)Anti-F9/Factor IX Reference Antibody (emicizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00537-1-sec-hplc.jpgAnti-F9 / Factor IX Reference Antibody (emicizumab)The purity of Anti-F9/Factor IX Reference Antibody (emicizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284112026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-4-sds-page.jpgAnti-ERBB3 / HER3 Reference Antibody (patritumab)Anti-ERBB3/HER3 Reference Antibody (patritumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-4-sec-hplc.jpgAnti-ERBB3 / HER3 Reference Antibody (patritumab)The purity of Anti-ERBB3/HER3 Reference Antibody (patritumab)is more than 99.19%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-4-od450.jpgAnti-ERBB3 / HER3 Reference Antibody (patritumab)Immobilized human HER3 His at 2 &mug/mL can bind Anti-ERBB3/HER3 Reference Antibody (patritumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-4-facs.jpgAnti-ERBB3 / HER3 Reference Antibody (patritumab)Human HER3 HEK293 cells were stained with Anti-ERBB3/HER3 Reference Antibody (patritumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1284122026-03-10T04:38:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-5-sds-page.jpgAnti-ERBB3/ HER3 Reference Antibody (patritumab deruxtecan)Anti-ERBB3/ HER3 Reference Antibody (patritumab deruxtecan) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-5-sec-hplc.jpgAnti-ERBB3/ HER3 Reference Antibody (patritumab deruxtecan)The purity of Anti-ERBB3/ HER3 Reference Antibody (patritumab deruxtecan)is more than 99.19%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-5-od450.jpgAnti-ERBB3/ HER3 Reference Antibody (patritumab deruxtecan)Immobilized human HER3 His at 2 &mug/mL can bind Anti-ERBB3/ HER3 Reference Antibody (patritumab deruxtecan) https://www.bosterbio.com/catalog/product/view/id/1284132026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-6-sds-page.jpgAnti-ERBB3 / HER3 Reference Antibody (lumretuzumab)Anti-ERBB3/HER3 Reference Antibody (lumretuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-6-sec-hplc.jpgAnti-ERBB3 / HER3 Reference Antibody (lumretuzumab)The purity of Anti-ERBB3/HER3 Reference Antibody (lumretuzumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-6-od450.jpgAnti-ERBB3 / HER3 Reference Antibody (lumretuzumab)Immobilized human HER3 His at 2 &mug/mL can bind Anti-ERBB3/HER3 Reference Antibody (lumretuzumab) https://www.bosterbio.com/catalog/product/view/id/1284142026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-7-sds-page.jpgAnti-ERBB3 / HER3 Reference Antibody (barecetamab)Anti-ERBB3/HER3 Reference Antibody (barecetamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-7-sec-hplc.jpgAnti-ERBB3 / HER3 Reference Antibody (barecetamab)The purity of Anti-ERBB3/HER3 Reference Antibody (barecetamab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-7-od450.jpgAnti-ERBB3 / HER3 Reference Antibody (barecetamab)Immobilized human HER3 His at 2 &mug/mL can bind Anti-ERBB3/HER3 Reference Antibody (barecetamab) https://www.bosterbio.com/catalog/product/view/id/1284152026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-8-sds-page.jpgAnti-ERBB3 / HER3 Reference Antibody (seribantumab)Anti-ERBB3/HER3 Reference Antibody (seribantumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-8-sec-hplc.jpgAnti-ERBB3 / HER3 Reference Antibody (seribantumab)The purity of Anti-ERBB3/HER3 Reference Antibody (seribantumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284162026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-9-sds-page.jpgAnti-ERBB3/ HER3 Reference Antibody (patritumab-MMAE)Anti-ERBB3/ HER3 Reference Antibody (patritumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00539-9-sec-hplc.jpgAnti-ERBB3/ HER3 Reference Antibody (patritumab-MMAE)The purity of Anti-ERBB3/ HER3 Reference Antibody (patritumab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284172026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-8-sds-page.jpgAnti-PTPRC / CD45 Reference Antibody (Novartis patent anti-CD45)Anti-PTPRC/CD45 Reference Antibody (Novartis patent anti-CD45) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-8-sec-hplc.jpgAnti-PTPRC / CD45 Reference Antibody (Novartis patent anti-CD45)The purity of Anti-PTPRC/CD45 Reference Antibody (Novartis patent anti-CD45)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-8-od450.jpgAnti-PTPRC / CD45 Reference Antibody (Novartis patent anti-CD45)Immobilized human IL-18 His at4 &mug/mL can bind Anti-PTPRC/CD45 Reference Antibody (Novartis patent anti-CD45) https://www.bosterbio.com/catalog/product/view/id/1284182026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-9-sds-page.jpgAnti-PTPRC / CD45 Reference Antibody (apamistamab)Anti-PTPRC/CD45 Reference Antibody (apamistamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00555-9-sec-hplc.jpgAnti-PTPRC / CD45 Reference Antibody (apamistamab)The purity of Anti-PTPRC/CD45 Reference Antibody (apamistamab)is more than 99.81% https://www.bosterbio.com/catalog/product/view/id/1284192026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-5-sds-page.jpgAnti-Fibronectin Reference Antibody (radretumab)Anti-Fibronectin Reference Antibody (radretumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-5-sec-hplc.jpgAnti-Fibronectin Reference Antibody (radretumab)The purity of Anti-Fibronectin Reference Antibody (radretumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284202026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-6-sds-page.jpgAnti-Fibronectin Reference Antibody (L19-TNF)Anti-Fibronectin Reference Antibody (L19-TNF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00564-6-sec-hplc.jpgAnti-Fibronectin Reference Antibody (L19-TNF)The purity of Anti-Fibronectin Reference Antibody (L19-TNF)is more than 98.36% https://www.bosterbio.com/catalog/product/view/id/1284212026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00570-3-sds-page.jpgAnti-CD2 Reference Antibody (siplizumab)Anti-CD2 Reference Antibody (siplizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00570-3-sec-hplc.jpgAnti-CD2 Reference Antibody (siplizumab)The purity of Anti-CD2 Reference Antibody (siplizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284222026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00573-1-sds-page.jpgAnti-Complement C2 Reference Antibody (ARGX-117)Anti-Complement C2 Reference Antibody (ARGX-117) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00573-1-sec-hplc.jpgAnti-Complement C2 Reference Antibody (ARGX-117)The purity of Anti-Complement C2 Reference Antibody (ARGX-117)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00573-1-od450.jpgAnti-Complement C2 Reference Antibody (ARGX-117)Immobilized human Complement C2 Protein at 2 &mug/mL can bind Anti-Complement C2 Reference Antibody (ARGX-117) https://www.bosterbio.com/catalog/product/view/id/1284232026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00576-1-sds-page.jpgAnti-TSHR Reference Antibody (K1-70)Anti-TSHR Reference Antibody (K1-70) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00576-1-sec-hplc.jpgAnti-TSHR Reference Antibody (K1-70)The purity of Anti-TSHR Reference Antibody (K1-70)is more than 98.3% https://www.bosterbio.com/catalog/product/view/id/1284242026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00578-1-sds-page.jpgAnti-EphA2 Reference Antibody (MEDI-547)Anti-EphA2 Reference Antibody (MEDI-547) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00578-1-sec-hplc.jpgAnti-EphA2 Reference Antibody (MEDI-547)The purity of Anti-EphA2 Reference Antibody (MEDI-547)is more than 96.63% https://www.bosterbio.com/catalog/product/view/id/1284252026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00578-2-sds-page.jpgAnti-EphA2 Reference Antibody (Sanofi Aventis patent anti-EphA2)Anti-EphA2 Reference Antibody (Sanofi Aventis patent anti-EphA2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00578-2-sec-hplc.jpgAnti-EphA2 Reference Antibody (Sanofi Aventis patent anti-EphA2)The purity of Anti-EphA2 Reference Antibody (Sanofi Aventis patent anti-EphA2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284262026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00591-3-sds-page.jpgAnti-TfR Reference Antibody (Jr-141)Anti-TfR Reference Antibody (Jr-141) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00591-3-sec-hplc.jpgAnti-TfR Reference Antibody (Jr-141)The purity of Anti-TfR Reference Antibody (Jr-141)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00591-3-od450.jpgAnti-TfR Reference Antibody (Jr-141)Immobilized human Transferrin R https://www.bosterbio.com/catalog/product/view/id/1284272026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00594-2-sds-page.jpgAnti-Adrenomedullin Reference Antibody (enibarcimab)Anti-Adrenomedullin Reference Antibody (enibarcimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00594-2-sec-hplc.jpgAnti-Adrenomedullin Reference Antibody (enibarcimab)The purity of Anti-Adrenomedullin Reference Antibody (enibarcimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284282026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00597-3-sds-page.jpgAnti-DPP4 / CD26 Reference Antibody (begelomab)Anti-DPP4/CD26 Reference Antibody (begelomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00597-3-sec-hplc.jpgAnti-DPP4 / CD26 Reference Antibody (begelomab)The purity of Anti-DPP4/CD26 Reference Antibody (begelomab)is more than 98.65 % https://www.bosterbio.com/catalog/product/view/id/1284292026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00617-3-sds-page.jpgAnti-CCL5 / RANTES Reference Antibody (NI-0701)Anti-CCL5/RANTES Reference Antibody (NI-0701) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00617-3-sec-hplc.jpgAnti-CCL5 / RANTES Reference Antibody (NI-0701)The purity of Anti-CCL5/RANTES Reference Antibody (NI-0701)is more than 98.94% https://www.bosterbio.com/catalog/product/view/id/1284302026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00617-4-sds-page.jpgAnti-CCL5 / RANTES Reference Antibody (VLST-002)Anti-CCL5/RANTES Reference Antibody (VLST-002) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00617-4-sec-hplc.jpgAnti-CCL5 / RANTES Reference Antibody (VLST-002)The purity of Anti-CCL5/RANTES Reference Antibody (VLST-002)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284312026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00620-2-sds-page.jpgAnti-CSF1 / M-CSF Reference Antibody (lacnotuzumab)Anti-CSF1/M-CSF Reference Antibody (lacnotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00620-2-sec-hplc.jpgAnti-CSF1 / M-CSF Reference Antibody (lacnotuzumab)The purity of Anti-CSF1/M-CSF Reference Antibody (lacnotuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284322026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00623-2-sds-page.jpgAnti-VEGFC Reference Antibody (VGX100)Anti-VEGFC Reference Antibody (VGX100) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00623-2-sec-hplc.jpgAnti-VEGFC Reference Antibody (VGX100)The purity of Anti-VEGFC Reference Antibody (VGX100)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00623-2-od450.jpgAnti-VEGFC Reference Antibody (VGX100)Immobilized human VEGFC His at 2 &mug/mL can bind Anti-VEGFC Reference Antibody (VGX100) https://www.bosterbio.com/catalog/product/view/id/1284332026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-2-sds-page.jpgAnti-DKK1 Reference Antibody (BHQ-880)Anti-DKK1 Reference Antibody (BHQ-880) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-2-sec-hplc.jpgAnti-DKK1 Reference Antibody (BHQ-880)The purity of Anti-DKK1 Reference Antibody (BHQ-880)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284342026-03-10T04:39:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-3-sds-page.jpgAnti-DKK1 Reference Antibody (BHQ880)Anti-DKK1 Reference Antibody (BHQ880) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00632-3-sec-hplc.jpgAnti-DKK1 Reference Antibody (BHQ880)The purity of Anti-DKK1 Reference Antibody (BHQ880)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284352026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-2-sds-page.jpgAnti-Osteopontin Reference Antibody (ASK8007)Anti-Osteopontin Reference Antibody (ASK8007) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 97.4%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00634-2-sec-hplc.jpgAnti-Osteopontin Reference Antibody (ASK8007)The purity of Anti-Osteopontin Reference Antibody (ASK8007)is more than 98.51% https://www.bosterbio.com/catalog/product/view/id/1284362026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00637-1-sds-page.jpgAnti-SERPINE1 Reference Antibody (Sanofi patent anti-PAI-1)Anti-SERPINE1 Reference Antibody (Sanofi patent anti-PAI-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00637-1-sec-hplc.jpgAnti-SERPINE1 Reference Antibody (Sanofi patent anti-PAI-1)The purity of Anti-SERPINE1 Reference Antibody (Sanofi patent anti-PAI-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284372026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00652-3-sds-page.jpgAnti-L-selectin Reference Antibody (Aselizumab)Anti-L-selectin Reference Antibody (Aselizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00652-3-sec-hplc.jpgAnti-L-selectin Reference Antibody (Aselizumab)The purity of Anti-L-selectin Reference Antibody (Aselizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284382026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00657-2-sds-page.jpgAnti-TIM-3 / HAVCR2 / CD366 Reference Antibody (cobolimab)Anti-TIM-3/HAVCR2/CD366 Reference Antibody (cobolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00657-2-sec-hplc.jpgAnti-TIM-3 / HAVCR2 / CD366 Reference Antibody (cobolimab)The purity of Anti-TIM-3/HAVCR2/CD366 Reference Antibody (cobolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284392026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00657-3-sds-page.jpgAnti-TIM-3 / HAVCR2 / CD366 Reference Antibody (sabatolimab)Anti-TIM-3/HAVCR2/CD366 Reference Antibody (sabatolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00657-3-sec-hplc.jpgAnti-TIM-3 / HAVCR2 / CD366 Reference Antibody (sabatolimab)The purity of Anti-TIM-3/HAVCR2/CD366 Reference Antibody (sabatolimab)is more than 98.49% https://www.bosterbio.com/catalog/product/view/id/1284402026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00657-4-sds-page.jpgAnti-TIM-3 / HAVCR2 / CD366 Reference Antibody (Surzebiclimab)Anti-TIM-3/HAVCR2/CD366 Reference Antibody (Surzebiclimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00657-4-sec-hplc.jpgAnti-TIM-3 / HAVCR2 / CD366 Reference Antibody (Surzebiclimab)The purity of Anti-TIM-3/HAVCR2/CD366 Reference Antibody (Surzebiclimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284412026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00661-1-sds-page.jpgAnti-NKG2D / CD314 Reference Antibody (tesnatilimab)Anti-NKG2D/CD314 Reference Antibody (tesnatilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00661-1-sec-hplc.jpgAnti-NKG2D / CD314 Reference Antibody (tesnatilimab)The purity of Anti-NKG2D/CD314 Reference Antibody (tesnatilimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00661-1-od450.jpgAnti-NKG2D / CD314 Reference Antibody (tesnatilimab)Immobilized human NKG2D His at 2 &mug/mL can bind Anti-NKG2D/CD314 Reference Antibody (tesnatilimab) https://www.bosterbio.com/catalog/product/view/id/1284422026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00663-2-sds-page.jpgAnti-CXCR5 / CD185 Reference Antibody (SAR113244)Anti-CXCR5/CD185 Reference Antibody (SAR113244) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 98.9%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00663-2-sec-hplc.jpgAnti-CXCR5 / CD185 Reference Antibody (SAR113244)The purity of Anti-CXCR5/CD185 Reference Antibody (SAR113244)is more than 98.97% https://www.bosterbio.com/catalog/product/view/id/1284432026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00664-4-sds-page.jpgAnti-PVR / CD155 Reference Antibody (Ntx1088)Anti-PVR/CD155 Reference Antibody (Ntx1088) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00664-4-sec-hplc.jpgAnti-PVR / CD155 Reference Antibody (Ntx1088)The purity of Anti-PVR/CD155 Reference Antibody (Ntx1088)is more than 99.38%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00664-4-facs.jpgAnti-PVR / CD155 Reference Antibody (Ntx1088)Human CD155 CHOK cells were stained with Anti-PVR/CD155 Reference Antibody (Ntx1088) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1284442026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00666-1-sds-page.jpgAnti-TMPRSS2 Reference Antibody (Regeneron patent anti-TMPRSS2 )Anti-TMPRSS2 Reference Antibody (Regeneron patent anti-TMPRSS2 ) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00666-1-sec-hplc.jpgAnti-TMPRSS2 Reference Antibody (Regeneron patent anti-TMPRSS2 )The purity of Anti-TMPRSS2 Reference Antibody (Regeneron patent anti-TMPRSS2 )is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284452026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00690-sds-page.jpgAnti-EphB4 Reference Antibody (Morphosys patent anti-EphB4)Anti-EphB4 Reference Antibody (Morphosys patent anti-EphB4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00690-sec-hplc.jpgAnti-EphB4 Reference Antibody (Morphosys patent anti-EphB4)The purity of Anti-EphB4 Reference Antibody (Morphosys patent anti-EphB4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284462026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00690-1-sds-page.jpgAnti-EphB4 Reference Antibody (VasGene patent anti-EphB4)Anti-EphB4 Reference Antibody (VasGene patent anti-EphB4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00690-1-sec-hplc.jpgAnti-EphB4 Reference Antibody (VasGene patent anti-EphB4)The purity of Anti-EphB4 Reference Antibody (VasGene patent anti-EphB4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284472026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-3-sds-page.jpgAnti-TrkA / NTRK1 Reference Antibody (GBR 900)Anti-TrkA/NTRK1 Reference Antibody (GBR 900) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00706-3-sec-hplc.jpgAnti-TrkA / NTRK1 Reference Antibody (GBR 900)The purity of Anti-TrkA/NTRK1 Reference Antibody (GBR 900)is more than 97.29% https://www.bosterbio.com/catalog/product/view/id/1284482026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00713-2-sds-page.jpgAnti-ANO1 / TMEM16A Reference Antibody (Novartis patent anti-TMEM16A )Anti-ANO1/TMEM16A Reference Antibody (Novartis patent anti-TMEM16A ) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00713-2-sec-hplc.jpgAnti-ANO1 / TMEM16A Reference Antibody (Novartis patent anti-TMEM16A )The purity of Anti-ANO1/TMEM16A Reference Antibody (Novartis patent anti-TMEM16A )is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284492026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00746-3-sds-page.jpgAnti-TNFSF1 / TNFb/ LT alpha Reference Antibody (pateclizumab)Anti-TNFSF1/TNFb/ LT alpha Reference Antibody (pateclizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00746-3-sec-hplc.jpgAnti-TNFSF1 / TNFb/ LT alpha Reference Antibody (pateclizumab)The purity of Anti-TNFSF1/TNFb/ LT alpha Reference Antibody (pateclizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284502026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00748-sds-page.jpgAnti-CCL20 Reference Antibody (GSK3050002)Anti-CCL20 Reference Antibody (GSK3050002) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00748-sec-hplc.jpgAnti-CCL20 Reference Antibody (GSK3050002)The purity of Anti-CCL20 Reference Antibody (GSK3050002)is more than 98.28% https://www.bosterbio.com/catalog/product/view/id/1284512026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00753-sds-page.jpgAnti-GLP1R Reference Antibody (Centocor patent anti-GLP-1R)Anti-GLP1R Reference Antibody (Centocor patent anti-GLP-1R) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00753-sec-hplc.jpgAnti-GLP1R Reference Antibody (Centocor patent anti-GLP-1R)The purity of Anti-GLP1R Reference Antibody (Centocor patent anti-GLP-1R)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284522026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00755-sds-page.jpgAnti-CCR4 / CD194 Reference Antibody (mogamulizumab)Anti-CCR4/CD194 Reference Antibody (mogamulizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00755-sec-hplc.jpgAnti-CCR4 / CD194 Reference Antibody (mogamulizumab)The purity of Anti-CCR4/CD194 Reference Antibody (mogamulizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284532026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00759-4-sds-page.jpgAnti-TBFbR2 Reference Antibody (LY3022859)Anti-TBFbR2 Reference Antibody (LY3022859) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00759-4-sec-hplc.jpgAnti-TBFbR2 Reference Antibody (LY3022859)The purity of Anti-TBFbR2 Reference Antibody (LY3022859)is more than 98.25% https://www.bosterbio.com/catalog/product/view/id/1284542026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00769-3-sds-page.jpgAnti-FGFR4 / CD334 Reference Antibody (U3-1784)Anti-FGFR4/CD334 Reference Antibody (U3-1784) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00769-3-sec-hplc.jpgAnti-FGFR4 / CD334 Reference Antibody (U3-1784)The purity of Anti-FGFR4/CD334 Reference Antibody (U3-1784)is more than 99.1%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00769-3-od450.jpgAnti-FGFR4 / CD334 Reference Antibody (U3-1784)Immobilized human FGFR4 FC at 2 &mug/mL can bind Anti-FGFR4/CD334 Reference Antibody (U3-1784) https://www.bosterbio.com/catalog/product/view/id/1284552026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00770-1-sds-page.jpgAnti-NAMPT Reference Antibody (Alt-100)Anti-NAMPT Reference Antibody (Alt-100) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00770-1-sec-hplc.jpgAnti-NAMPT Reference Antibody (Alt-100)The purity of Anti-NAMPT Reference Antibody (Alt-100)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284562026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-5-sds-page.jpgAnti-Integrin b1 / ITGB1 / CD29 Reference Antibody (OS2966)Anti-Integrin b1/ITGB1/CD29 Reference Antibody (OS2966) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00772-5-sec-hplc.jpgAnti-Integrin b1 / ITGB1 / CD29 Reference Antibody (OS2966)The purity of Anti-Integrin b1/ITGB1/CD29 Reference Antibody (OS2966)is more than 99.25% https://www.bosterbio.com/catalog/product/view/id/1284572026-03-10T04:39:01+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00780-5-sds-page.jpgAnti-LAMP1 / CD107a Reference Antibody ( SAR428926)Anti-LAMP1/CD107a Reference Antibody ( SAR428926) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00780-5-sec-hplc.jpgAnti-LAMP1 / CD107a Reference Antibody ( SAR428926)The purity of Anti-LAMP1/CD107a Reference Antibody ( SAR428926)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284582026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00793-2-sds-page.jpgAnti-ERG Reference Antibody (Jackson Foundation patent anti-ERG)Anti-ERG Reference Antibody (Jackson Foundation patent anti-ERG) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00793-2-sec-hplc.jpgAnti-ERG Reference Antibody (Jackson Foundation patent anti-ERG)The purity of Anti-ERG Reference Antibody (Jackson Foundation patent anti-ERG)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284592026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00798-1-sds-page.jpgAnti-ACVR1 / ALK-2 Reference Antibody (DS-6016a)Anti-ACVR1/ALK-2 Reference Antibody (DS-6016a) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00798-1-sec-hplc.jpgAnti-ACVR1 / ALK-2 Reference Antibody (DS-6016a)The purity of Anti-ACVR1/ALK-2 Reference Antibody (DS-6016a)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284602026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-sds-page.jpgAnti-IL-4Ra / CD124 Reference Antibody (dupilumab)Anti-IL-4Ra/CD124 Reference Antibody (dupilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-sec-hplc.jpgAnti-IL-4Ra / CD124 Reference Antibody (dupilumab)The purity of Anti-IL-4Ra/CD124 Reference Antibody (dupilumab)is more than 96.86%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-od450.jpgAnti-IL-4Ra / CD124 Reference Antibody (dupilumab)Immobilized human IL4RA His at 2 &mug/mL can bind Anti-IL-4Ra/CD124 Reference Antibody (dupilumab) https://www.bosterbio.com/catalog/product/view/id/1284612026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-1-sds-page.jpgAnti-IL-4 Reference Antibody (pascolizumab)Anti-IL-4 Reference Antibody (pascolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-1-sec-hplc.jpgAnti-IL-4 Reference Antibody (pascolizumab)The purity of Anti-IL-4 Reference Antibody (pascolizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284622026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-2-sds-page.jpgAnti-IL-4Ra / CD124 Reference Antibody (Manfidokimab)Anti-IL-4Ra/CD124 Reference Antibody (Manfidokimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-2-sec-hplc.jpgAnti-IL-4Ra / CD124 Reference Antibody (Manfidokimab)The purity of Anti-IL-4Ra/CD124 Reference Antibody (Manfidokimab)is more than 99.14% https://www.bosterbio.com/catalog/product/view/id/1284632026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-3-sds-page.jpgAnti-IL-4Ra / CD124 Reference Antibody (MEDI2045)Anti-IL-4Ra/CD124 Reference Antibody (MEDI2045) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00807-3-sec-hplc.jpgAnti-IL-4Ra / CD124 Reference Antibody (MEDI2045)The purity of Anti-IL-4Ra/CD124 Reference Antibody (MEDI2045)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284642026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00812-6-sds-page.jpgAnti-CD163 Reference Antibody (OR2805)Anti-CD163 Reference Antibody (OR2805) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00812-6-sec-hplc.jpgAnti-CD163 Reference Antibody (OR2805)The purity of Anti-CD163 Reference Antibody (OR2805)is more than 93.25% https://www.bosterbio.com/catalog/product/view/id/1284652026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00815-1-sds-page.jpgAnti-MUSK Reference Antibody (Argenx patent anti-MuSK)Anti-MUSK Reference Antibody (Argenx patent anti-MuSK) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00815-1-sec-hplc.jpgAnti-MUSK Reference Antibody (Argenx patent anti-MuSK)The purity of Anti-MUSK Reference Antibody (Argenx patent anti-MuSK)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284662026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00852-sds-page.jpgAnti-Complement Factor P / Properdin Reference Antibody (Novelmed patent anti-Properdin)Anti-Complement Factor P/Properdin Reference Antibody (Novelmed patent anti-Properdin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00852-sec-hplc.jpgAnti-Complement Factor P / Properdin Reference Antibody (Novelmed patent anti-Properdin)The purity of Anti-Complement Factor P/Properdin Reference Antibody (Novelmed patent anti-Properdin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284672026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00867-2-sds-page.jpgAnti-TNFRSF9 / 4-1BB / CD137 Reference Antibody (utomilumab)Anti-TNFRSF9/4-1BB/CD137 Reference Antibody (utomilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00867-2-sec-hplc.jpgAnti-TNFRSF9 / 4-1BB / CD137 Reference Antibody (utomilumab)The purity of Anti-TNFRSF9/4-1BB/CD137 Reference Antibody (utomilumab)is more than 98.78%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00867-2-od450.jpgAnti-TNFRSF9 / 4-1BB / CD137 Reference Antibody (utomilumab)Immobilized human TNFRSF9/4 1BB/CD137 https://www.bosterbio.com/catalog/product/view/id/1284682026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00867-3-sds-page.jpgAnti-TNFRSF9 / 4-1BB / CD137 Reference Antibody (urelumab)Anti-TNFRSF9/4-1BB/CD137 Reference Antibody (urelumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00867-3-sec-hplc.jpgAnti-TNFRSF9 / 4-1BB / CD137 Reference Antibody (urelumab)The purity of Anti-TNFRSF9/4-1BB/CD137 Reference Antibody (urelumab)is more than 97.3%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00867-3-od450.jpgAnti-TNFRSF9 / 4-1BB / CD137 Reference Antibody (urelumab)Immobilized N His HSA TNFSF9/4 1BB at 2 &mug/mL can bind Anti-TNFRSF9/4-1BB/CD137 Reference Antibody (urelumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00867-3-facs.jpgAnti-TNFRSF9 / 4-1BB / CD137 Reference Antibody (urelumab)4-1BB-NF-KB-Jurkat cells were stained with Anti-TNFRSF9/4-1BB/CD137 Reference Antibody (urelumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1284692026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00871-1-sds-page.jpgAnti-CXCL4 / PF4 Reference Antibody (U.Penn. patent anti-PF4)Anti-CXCL4/PF4 Reference Antibody (U.Penn. patent anti-PF4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00871-1-sec-hplc.jpgAnti-CXCL4 / PF4 Reference Antibody (U.Penn. patent anti-PF4)The purity of Anti-CXCL4/PF4 Reference Antibody (U.Penn. patent anti-PF4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284702026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-sds-page.jpgAnti-DLL4 Reference Antibody (navicixizumab)Anti-DLL4 Reference Antibody (navicixizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-sec-hplc.jpgAnti-DLL4 Reference Antibody (navicixizumab)The purity of Anti-DLL4 Reference Antibody (navicixizumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-od450.jpgAnti-DLL4 Reference Antibody (navicixizumab)Immobilized human VEGF165 His at 2 &mug/mL can bind Anti-DLL4 Reference Antibody (navicixizumab) https://www.bosterbio.com/catalog/product/view/id/1284712026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-1-sds-page.jpgAnti-DLL4 Reference Antibody (enoticumab)Anti-DLL4 Reference Antibody (enoticumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-1-sec-hplc.jpgAnti-DLL4 Reference Antibody (enoticumab)The purity of Anti-DLL4 Reference Antibody (enoticumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-1-od450.jpgAnti-DLL4 Reference Antibody (enoticumab)Immobilized human DLL4 His at 2 &mug/mL can bind Anti-DLL4 Reference Antibody (enoticumab) https://www.bosterbio.com/catalog/product/view/id/1284722026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-2-sds-page.jpgAnti-DLL4 Reference Antibody (Smart Targeting patent anti-DLL4)Anti-DLL4 Reference Antibody (Smart Targeting patent anti-DLL4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-2-sec-hplc.jpgAnti-DLL4 Reference Antibody (Smart Targeting patent anti-DLL4)The purity of Anti-DLL4 Reference Antibody (Smart Targeting patent anti-DLL4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284732026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-3-sds-page.jpgAnti-DLL4 Reference Antibody (demcizumab)Anti-DLL4 Reference Antibody (demcizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00875-3-sec-hplc.jpgAnti-DLL4 Reference Antibody (demcizumab)The purity of Anti-DLL4 Reference Antibody (demcizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284742026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00882-sds-page.jpgAnti-CX3CL1 / Fractalkine Reference Antibody (quetmolimab)Anti-CX3CL1/Fractalkine Reference Antibody (quetmolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00882-sec-hplc.jpgAnti-CX3CL1 / Fractalkine Reference Antibody (quetmolimab)The purity of Anti-CX3CL1/Fractalkine Reference Antibody (quetmolimab)is more than 98.99% https://www.bosterbio.com/catalog/product/view/id/1284752026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00885-3-sds-page.jpgAnti-CD34 Reference Antibody (ITRI patent anti-CD34)Anti-CD34 Reference Antibody (ITRI patent anti-CD34) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00885-3-sec-hplc.jpgAnti-CD34 Reference Antibody (ITRI patent anti-CD34)The purity of Anti-CD34 Reference Antibody (ITRI patent anti-CD34)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284762026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-3-sds-page.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (ramucirumab)Anti-VEGFR2/KDR/CD309 Reference Antibody (ramucirumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-3-sec-hplc.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (ramucirumab)The purity of Anti-VEGFR2/KDR/CD309 Reference Antibody (ramucirumab)is more than 99.36%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-3-od450.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (ramucirumab)Immobilized human VGFR2 His at4 &mug/mL can bind Anti-VEGFR2/KDR/CD309 Reference Antibody (ramucirumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-3-facs.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (ramucirumab)VEGFR2/NFAT-Luci-HEK293 cells were stained with Anti-VEGFR2/KDR/CD309 Reference Antibody (ramucirumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1284772026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-4-sds-page.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (olinvacimab)Anti-VEGFR2/KDR/CD309 Reference Antibody (olinvacimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-4-sec-hplc.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (olinvacimab)The purity of Anti-VEGFR2/KDR/CD309 Reference Antibody (olinvacimab)is more than 99.12% https://www.bosterbio.com/catalog/product/view/id/1284782026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-5-sds-page.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (vulinacimab)Anti-VEGFR2/KDR/CD309 Reference Antibody (vulinacimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-5-sec-hplc.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (vulinacimab)The purity of Anti-VEGFR2/KDR/CD309 Reference Antibody (vulinacimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284792026-03-10T04:39:02+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-6-sds-page.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (AT001)Anti-VEGFR2/KDR/CD309 Reference Antibody (AT001) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-6-sec-hplc.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (AT001)The purity of Anti-VEGFR2/KDR/CD309 Reference Antibody (AT001)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284802026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-7-sds-page.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (alacizumAb)Anti-VEGFR2/KDR/CD309 Reference Antibody (alacizumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-7-sec-hplc.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (alacizumAb)The purity of Anti-VEGFR2/KDR/CD309 Reference Antibody (alacizumAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284812026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-8-sds-page.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (Imclone 6.64)Anti-VEGFR2/KDR/CD309 Reference Antibody (Imclone 6.64) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00901-8-sec-hplc.jpgAnti-VEGFR2 / KDR / CD309 Reference Antibody (Imclone 6.64)The purity of Anti-VEGFR2/KDR/CD309 Reference Antibody (Imclone 6.64)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284822026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00905-2-sds-page.jpgAnti-DDR1 / CD167a Reference Antibody (Imperial College anti-DDR1)Anti-DDR1/CD167a Reference Antibody (Imperial College anti-DDR1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00905-2-sec-hplc.jpgAnti-DDR1 / CD167a Reference Antibody (Imperial College anti-DDR1)The purity of Anti-DDR1/CD167a Reference Antibody (Imperial College anti-DDR1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284832026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00909-2-sds-page.jpgAnti-Orai1 Reference Antibody (Amgen patent anti-ORAI1)Anti-Orai1 Reference Antibody (Amgen patent anti-ORAI1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00909-2-sec-hplc.jpgAnti-Orai1 Reference Antibody (Amgen patent anti-ORAI1)The purity of Anti-Orai1 Reference Antibody (Amgen patent anti-ORAI1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284842026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-2-sds-page.jpgAnti-CSF2 / GM-CSF Reference Antibody (lenzilumab)Anti-CSF2/GM-CSF Reference Antibody (lenzilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-2-sec-hplc.jpgAnti-CSF2 / GM-CSF Reference Antibody (lenzilumab)The purity of Anti-CSF2/GM-CSF Reference Antibody (lenzilumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-2-od450.jpgAnti-CSF2 / GM-CSF Reference Antibody (lenzilumab)Immobilized human GM CSF Nhis at 2 &mug/mL can bind Anti-CSF2/GM-CSF Reference Antibody (lenzilumab) https://www.bosterbio.com/catalog/product/view/id/1284852026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-3-sds-page.jpgAnti-CSF2 / GM-CSF Reference Antibody (namilumab)Anti-CSF2/GM-CSF Reference Antibody (namilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-3-sec-hplc.jpgAnti-CSF2 / GM-CSF Reference Antibody (namilumab)The purity of Anti-CSF2/GM-CSF Reference Antibody (namilumab)is more than 90.29%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-3-od450.jpgAnti-CSF2 / GM-CSF Reference Antibody (namilumab)Immobilized human GM CSF Nhis at 2 &mug/mL can bind Anti-CSF2/GM-CSF Reference Antibody (namilumab) https://www.bosterbio.com/catalog/product/view/id/1284862026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-4-sds-page.jpgAnti-CSF2 / GM-CSF Reference Antibody (gimsilumab)Anti-CSF2/GM-CSF Reference Antibody (gimsilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-4-sec-hplc.jpgAnti-CSF2 / GM-CSF Reference Antibody (gimsilumab)The purity of Anti-CSF2/GM-CSF Reference Antibody (gimsilumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284872026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-5-sds-page.jpgAnti-CSF2 / GM-CSF Reference Antibody (otilimab)Anti-CSF2/GM-CSF Reference Antibody (otilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-5-sec-hplc.jpgAnti-CSF2 / GM-CSF Reference Antibody (otilimab)The purity of Anti-CSF2/GM-CSF Reference Antibody (otilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284882026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-6-sds-page.jpgAnti-CSF2 / GM-CSF Reference Antibody (plonmarlimab)Anti-CSF2/GM-CSF Reference Antibody (plonmarlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-6-sec-hplc.jpgAnti-CSF2 / GM-CSF Reference Antibody (plonmarlimab)The purity of Anti-CSF2/GM-CSF Reference Antibody (plonmarlimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1284892026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-7-sds-page.jpgAnti-CSF2 / GM-CSF Reference Antibody (Theraclone patent anti-GM-CSF)Anti-CSF2/GM-CSF Reference Antibody (Theraclone patent anti-GM-CSF) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00911-7-sec-hplc.jpgAnti-CSF2 / GM-CSF Reference Antibody (Theraclone patent anti-GM-CSF)The purity of Anti-CSF2/GM-CSF Reference Antibody (Theraclone patent anti-GM-CSF)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284902026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00913-6-sds-page.jpgAnti-TYRO3 Reference Antibody (ELB031)Anti-TYRO3 Reference Antibody (ELB031) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00913-6-sec-hplc.jpgAnti-TYRO3 Reference Antibody (ELB031)The purity of Anti-TYRO3 Reference Antibody (ELB031)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284912026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00914-5-sds-page.jpgAnti-CD59 Reference Antibody ( Mellitus patent anti-CD59)Anti-CD59 Reference Antibody ( Mellitus patent anti-CD59) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00914-5-sec-hplc.jpgAnti-CD59 Reference Antibody ( Mellitus patent anti-CD59)The purity of Anti-CD59 Reference Antibody ( Mellitus patent anti-CD59)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284922026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00914-6-sds-page.jpgAnti-CD59 Reference Antibody (Quark patent anti-CD59)Anti-CD59 Reference Antibody (Quark patent anti-CD59) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00914-6-sec-hplc.jpgAnti-CD59 Reference Antibody (Quark patent anti-CD59)The purity of Anti-CD59 Reference Antibody (Quark patent anti-CD59)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284932026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00918-1-sds-page.jpgAnti-IL-12 (IL-12a & IL-12b) Reference Antibody (briakinumab)Anti-IL-12 (IL-12a & IL-12b) Reference Antibody (briakinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00918-1-sec-hplc.jpgAnti-IL-12 (IL-12a & IL-12b) Reference Antibody (briakinumab)The purity of Anti-IL-12 (IL-12a & IL-12b) Reference Antibody (briakinumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284942026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00920-1-sds-page.jpgAnti-SCN9a / Nav1.7 Reference Antibody (Duke anti-NAv1.7)Anti-SCN9a/Nav1.7 Reference Antibody (Duke anti-NAv1.7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00920-1-sec-hplc.jpgAnti-SCN9a / Nav1.7 Reference Antibody (Duke anti-NAv1.7)The purity of Anti-SCN9a/Nav1.7 Reference Antibody (Duke anti-NAv1.7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284952026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00923-3-sds-page.jpgAnti-CEACAM1 / CD66a Reference Antibody (CM-24)Anti-CEACAM1/CD66a Reference Antibody (CM-24) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00923-3-sec-hplc.jpgAnti-CEACAM1 / CD66a Reference Antibody (CM-24)The purity of Anti-CEACAM1/CD66a Reference Antibody (CM-24)is more than 96.33%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00923-3-od450.jpgAnti-CEACAM1 / CD66a Reference Antibody (CM-24)Immobilized human CEACAM1 (C 6His) at 2 &mug/mL can bind Anti-CEACAM1/CD66a Reference Antibody (CM-24) https://www.bosterbio.com/catalog/product/view/id/1284962026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00923-4-sds-page.jpgAnti-CEACAM1 / CD66a Reference Antibody (Chaim Sheba Med. Cntr. patent anti-CEACAM1)Anti-CEACAM1/CD66a Reference Antibody (Chaim Sheba Med. Cntr. patent anti-CEACAM1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00923-4-sec-hplc.jpgAnti-CEACAM1 / CD66a Reference Antibody (Chaim Sheba Med. Cntr. patent anti-CEACAM1)The purity of Anti-CEACAM1/CD66a Reference Antibody (Chaim Sheba Med. Cntr. patent anti-CEACAM1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1284972026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-2-sds-page.jpgAnti-GDF8 / Myostatin Reference Antibody (apitegromab)Anti-GDF8/Myostatin Reference Antibody (apitegromab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-2-sec-hplc.jpgAnti-GDF8 / Myostatin Reference Antibody (apitegromab)The purity of Anti-GDF8/Myostatin Reference Antibody (apitegromab)is more than 94.94 % https://www.bosterbio.com/catalog/product/view/id/1284982026-03-10T04:39:03+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-3-sds-page.jpgAnti-GDF8 / Myostatin Reference Antibody (trevogrumab)Anti-GDF8/Myostatin Reference Antibody (trevogrumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-3-sec-hplc.jpgAnti-GDF8 / Myostatin Reference Antibody (trevogrumab)The purity of Anti-GDF8/Myostatin Reference Antibody (trevogrumab)is more than 96.57% https://www.bosterbio.com/catalog/product/view/id/1284992026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-4-sds-page.jpgAnti-GDF8 / Myostatin Reference Antibody (landogrozumab)Anti-GDF8/Myostatin Reference Antibody (landogrozumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-4-sec-hplc.jpgAnti-GDF8 / Myostatin Reference Antibody (landogrozumab)The purity of Anti-GDF8/Myostatin Reference Antibody (landogrozumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1285002026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-5-sds-page.jpgAnti-Siglec-3 / CD33 Reference Antibody (lintuzumAb)Anti-Siglec-3/CD33 Reference Antibody (lintuzumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-5-sec-hplc.jpgAnti-Siglec-3 / CD33 Reference Antibody (lintuzumAb)The purity of Anti-Siglec-3/CD33 Reference Antibody (lintuzumAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285012026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00934-2-sds-page.jpgAnti-BST2 / CD317 Reference Antibody (XmAb 5592)Anti-BST2/CD317 Reference Antibody (XmAb 5592) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00934-2-sec-hplc.jpgAnti-BST2 / CD317 Reference Antibody (XmAb 5592)The purity of Anti-BST2/CD317 Reference Antibody (XmAb 5592)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285022026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00934-3-sds-page.jpgAnti-BST2 / CD317 Reference Antibody (SBI Biotech patent anti-BST2)Anti-BST2/CD317 Reference Antibody (SBI Biotech patent anti-BST2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00934-3-sec-hplc.jpgAnti-BST2 / CD317 Reference Antibody (SBI Biotech patent anti-BST2)The purity of Anti-BST2/CD317 Reference Antibody (SBI Biotech patent anti-BST2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285032026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00936-2-sds-page.jpgAnti-Tenascin C Reference Antibody (tenatumomab)Anti-Tenascin C Reference Antibody (tenatumomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00936-2-sec-hplc.jpgAnti-Tenascin C Reference Antibody (tenatumomab)The purity of Anti-Tenascin C Reference Antibody (tenatumomab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1285042026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00963-2-sds-page.jpgAnti-IL-22 Reference Antibody (fezakinumab)Anti-IL-22 Reference Antibody (fezakinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00963-2-sec-hplc.jpgAnti-IL-22 Reference Antibody (fezakinumab)The purity of Anti-IL-22 Reference Antibody (fezakinumab)is more than 99.05%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00963-2-od450.jpgAnti-IL-22 Reference Antibody (fezakinumab)Immobilized human IL 22 https://www.bosterbio.com/catalog/product/view/id/1285052026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00989-sds-page.jpgAnti-F11 / Factor XI Reference Antibody (abelacimab)Anti-F11/Factor XI Reference Antibody (abelacimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00989-sec-hplc.jpgAnti-F11 / Factor XI Reference Antibody (abelacimab)The purity of Anti-F11/Factor XI Reference Antibody (abelacimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285062026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00989-1-sds-page.jpgAnti-F11 / Factor XI Reference Antibody (osocimab)Anti-F11/Factor XI Reference Antibody (osocimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00989-1-sec-hplc.jpgAnti-F11 / Factor XI Reference Antibody (osocimab)The purity of Anti-F11/Factor XI Reference Antibody (osocimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285072026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00991-2-sds-page.jpgAnti-Syndecan-1 / CD138 Reference Antibody (indatuximab)Anti-Syndecan-1/CD138 Reference Antibody (indatuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00991-2-sec-hplc.jpgAnti-Syndecan-1 / CD138 Reference Antibody (indatuximab)The purity of Anti-Syndecan-1/CD138 Reference Antibody (indatuximab)is more than 99% https://www.bosterbio.com/catalog/product/view/id/1285082026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00993-sds-page.jpgAnti-PLAUR / uPAR / CD87 Reference Antibody (ATN-658)Anti-PLAUR/uPAR/CD87 Reference Antibody (ATN-658) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00993-sec-hplc.jpgAnti-PLAUR / uPAR / CD87 Reference Antibody (ATN-658)The purity of Anti-PLAUR/uPAR/CD87 Reference Antibody (ATN-658)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285092026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01014-1-sds-page.jpgAnti-TNFRSF17 / BCMA / CD269 Reference Antibody (belantamab mafodotin)Anti-TNFRSF17/BCMA/CD269 Reference Antibody (belantamab mafodotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01014-1-sec-hplc.jpgAnti-TNFRSF17 / BCMA / CD269 Reference Antibody (belantamab mafodotin)The purity of Anti-TNFRSF17/BCMA/CD269 Reference Antibody (belantamab mafodotin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285102026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01014-2-sds-page.jpgAnti-TNFRSF17 / BCMA / CD269 Reference Antibody (belantamab)Anti-TNFRSF17/BCMA/CD269 Reference Antibody (belantamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01014-2-sec-hplc.jpgAnti-TNFRSF17 / BCMA / CD269 Reference Antibody (belantamab)The purity of Anti-TNFRSF17/BCMA/CD269 Reference Antibody (belantamab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01014-2-facs.jpgAnti-TNFRSF17 / BCMA / CD269 Reference Antibody (belantamab)U266 cells were stained with Anti-TNFRSF17/BCMA/CD269 Reference Antibody (belantamab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1285112026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01025-4-sds-page.jpgAnti-DC-SIGN / CD209 Reference Antibody (INSERM patent anti-DC-SIGN)Anti-DC-SIGN/CD209 Reference Antibody (INSERM patent anti-DC-SIGN) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01025-4-sec-hplc.jpgAnti-DC-SIGN / CD209 Reference Antibody (INSERM patent anti-DC-SIGN)The purity of Anti-DC-SIGN/CD209 Reference Antibody (INSERM patent anti-DC-SIGN)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285122026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01041-2-sds-page.jpgAnti-ETBR Reference Antibody (DEDN6526A)Anti-ETBR Reference Antibody (DEDN6526A) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01041-2-sec-hplc.jpgAnti-ETBR Reference Antibody (DEDN6526A)The purity of Anti-ETBR Reference Antibody (DEDN6526A)is more than 99.05% https://www.bosterbio.com/catalog/product/view/id/1285132026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01052-3-sds-page.jpgAnti-TFPI Reference Antibody (concizumab)Anti-TFPI Reference Antibody (concizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01052-3-sec-hplc.jpgAnti-TFPI Reference Antibody (concizumab)The purity of Anti-TFPI Reference Antibody (concizumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01052-3-od450.jpgAnti-TFPI Reference Antibody (concizumab)Immobilized human TFPI https://www.bosterbio.com/catalog/product/view/id/1285142026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01052-4-sds-page.jpgAnti-TFPI Reference Antibody (marstacimab)Anti-TFPI Reference Antibody (marstacimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01052-4-sec-hplc.jpgAnti-TFPI Reference Antibody (marstacimab)The purity of Anti-TFPI Reference Antibody (marstacimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285152026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01052-5-sds-page.jpgAnti-TFPI Reference Antibody (befovacimab)Anti-TFPI Reference Antibody (befovacimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01052-5-sec-hplc.jpgAnti-TFPI Reference Antibody (befovacimab)The purity of Anti-TFPI Reference Antibody (befovacimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285162026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01081-1-sds-page.jpgAnti-PAR2 Reference Antibody (Amgen patent anti-PAR-2)Anti-PAR2 Reference Antibody (Amgen patent anti-PAR-2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01081-1-sec-hplc.jpgAnti-PAR2 Reference Antibody (Amgen patent anti-PAR-2)The purity of Anti-PAR2 Reference Antibody (Amgen patent anti-PAR-2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285172026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01081-2-sds-page.jpgAnti-PAR2 Reference Antibody (PAR650097)Anti-PAR2 Reference Antibody (PAR650097) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01081-2-sec-hplc.jpgAnti-PAR2 Reference Antibody (PAR650097)The purity of Anti-PAR2 Reference Antibody (PAR650097)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285182026-03-10T04:39:04+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01081-3-sds-page.jpgAnti-PAR2 Reference Antibody (Regeneron patent anti-PAR-2)Anti-PAR2 Reference Antibody (Regeneron patent anti-PAR-2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01081-3-sec-hplc.jpgAnti-PAR2 Reference Antibody (Regeneron patent anti-PAR-2)The purity of Anti-PAR2 Reference Antibody (Regeneron patent anti-PAR-2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285192026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01082-sds-page.jpgAnti-RHD / CD240d Reference Antibody (roledumab)Anti-RHD/CD240d Reference Antibody (roledumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01082-sec-hplc.jpgAnti-RHD / CD240d Reference Antibody (roledumab)The purity of Anti-RHD/CD240d Reference Antibody (roledumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285202026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01082-1-sds-page.jpgAnti-RHD / CD240d Reference Antibody (LFB Anti-RhD)Anti-RHD/CD240d Reference Antibody (LFB Anti-RhD) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01082-1-sec-hplc.jpgAnti-RHD / CD240d Reference Antibody (LFB Anti-RhD)The purity of Anti-RHD/CD240d Reference Antibody (LFB Anti-RhD)is more than 98.9% https://www.bosterbio.com/catalog/product/view/id/1285212026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01083-3-sds-page.jpgAnti-CA9 / CAIX Reference Antibody (girentuximab)Anti-CA9/CAIX Reference Antibody (girentuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01083-3-sec-hplc.jpgAnti-CA9 / CAIX Reference Antibody (girentuximab)The purity of Anti-CA9/CAIX Reference Antibody (girentuximab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1285222026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01083-4-sds-page.jpgAnti-CA9 / CAIX Reference Antibody (girentuximab-MMAE)Anti-CA9/CAIX Reference Antibody (girentuximab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01083-4-sec-hplc.jpgAnti-CA9 / CAIX Reference Antibody (girentuximab-MMAE)The purity of Anti-CA9/CAIX Reference Antibody (girentuximab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285232026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-3-sds-page.jpgAnti-IL-5 Reference Antibody (depemokimab)Anti-IL-5 Reference Antibody (depemokimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-3-sec-hplc.jpgAnti-IL-5 Reference Antibody (depemokimab)The purity of Anti-IL-5 Reference Antibody (depemokimab)is more than 98.75% https://www.bosterbio.com/catalog/product/view/id/1285242026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-2-sds-page.jpgAnti-IL-5 Reference Antibody (Abgenix anti-IL-5)Anti-IL-5 Reference Antibody (Abgenix anti-IL-5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01086-2-sec-hplc.jpgAnti-IL-5 Reference Antibody (Abgenix anti-IL-5)The purity of Anti-IL-5 Reference Antibody (Abgenix anti-IL-5)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285252026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01092-sds-page.jpgAnti-IL-1R1 / CD121a Reference Antibody (AMG 108)Anti-IL-1R1/CD121a Reference Antibody (AMG 108) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01092-sec-hplc.jpgAnti-IL-1R1 / CD121a Reference Antibody (AMG 108)The purity of Anti-IL-1R1/CD121a Reference Antibody (AMG 108)is more than 99.03% https://www.bosterbio.com/catalog/product/view/id/1285262026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01096-sds-page.jpgAnti-TSLP Reference Antibody (tezepelumab)Anti-TSLP Reference Antibody (tezepelumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01096-sec-hplc.jpgAnti-TSLP Reference Antibody (tezepelumab)The purity of Anti-TSLP Reference Antibody (tezepelumab)is more than 98.64%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01096-od450.jpgAnti-TSLP Reference Antibody (tezepelumab)Immobilized human TSLP His at 2 &mug/mL can bind Anti-TSLP Reference Antibody (tezepelumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01096-facs.jpgAnti-TSLP Reference Antibody (tezepelumab)Anti-TSLP Reference Antibody (tezepelumab)-induced FACS Blocking activity was evaluated using TSLPR/IL7R-CHO-K. The IC50 was approximately 0.0802 &mug/mL.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01096-syngenic-mc38-cell-model.jpgAnti-TSLP Reference Antibody (tezepelumab)Tezepelumab reduced levels of IL13 in BALF of OVA asthma model on B-hTSLP/hTSLPR mice. The result showed significant IL13 inhibition effects at 15 mpk. https://www.bosterbio.com/catalog/product/view/id/1285272026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01096-1-sds-page.jpgAnti-TSLP Reference Antibody (Schering patent anti-TSLP)Anti-TSLP Reference Antibody (Schering patent anti-TSLP) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01096-1-sec-hplc.jpgAnti-TSLP Reference Antibody (Schering patent anti-TSLP)The purity of Anti-TSLP Reference Antibody (Schering patent anti-TSLP)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285282026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-1-sds-page.jpgAnti-IL-23 Reference Antibody (guselkumab)Anti-IL-23 Reference Antibody (guselkumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-1-sec-hplc.jpgAnti-IL-23 Reference Antibody (guselkumab)The purity of Anti-IL-23 Reference Antibody (guselkumab)is more than 98.97%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-1-od450.jpgAnti-IL-23 Reference Antibody (guselkumab)Immobilized human IL 23P40 His at 2 &mug/mL can bind Anti-IL-23 Reference Antibody (guselkumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-1-od405.jpgAnti-IL-23 Reference Antibody (guselkumab)Anti-IL-23 Reference Antibody (guselkumab) induced report gene STAT3 activity was evaluated using Human IL23 HEK-Blue. The EC50 was approximately 0.0095 ug/mL. https://www.bosterbio.com/catalog/product/view/id/1285292026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-6-sds-page.jpgAnti-IL-23 Reference Antibody (mirikizumab)Anti-IL-23 Reference Antibody (mirikizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-6-sec-hplc.jpgAnti-IL-23 Reference Antibody (mirikizumab)The purity of Anti-IL-23 Reference Antibody (mirikizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285302026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-3-sds-page.jpgAnti-IL-23 Reference Antibody (LY2525623)Anti-IL-23 Reference Antibody (LY2525623) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-3-sec-hplc.jpgAnti-IL-23 Reference Antibody (LY2525623)The purity of Anti-IL-23 Reference Antibody (LY2525623)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285312026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-4-sds-page.jpgAnti-IL-23a Reference Antibody (tildrakizumab)Anti-IL-23a Reference Antibody (tildrakizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-4-sec-hplc.jpgAnti-IL-23a Reference Antibody (tildrakizumab)The purity of Anti-IL-23a Reference Antibody (tildrakizumab)is more than 99.53% https://www.bosterbio.com/catalog/product/view/id/1285322026-03-10T04:39:05+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-5-sds-page.jpgAnti-IL-23 Reference Antibody (brazikumab)Anti-IL-23 Reference Antibody (brazikumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-5-sec-hplc.jpgAnti-IL-23 Reference Antibody (brazikumab)The purity of Anti-IL-23 Reference Antibody (brazikumab)is more than 99.32% https://www.bosterbio.com/catalog/product/view/id/1285332026-03-10T04:39:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-2-sds-page.jpgAnti-IL-23a Reference Antibody (risankizumab)Anti-IL-23a Reference Antibody (risankizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-2-sec-hplc.jpgAnti-IL-23a Reference Antibody (risankizumab)The purity of Anti-IL-23a Reference Antibody (risankizumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01097-2-od450.jpgAnti-IL-23a Reference Antibody (risankizumab)Immobilized human IL 23P40 His at 2 &mug/mL can bind Anti-IL-23a Reference Antibody (risankizumab) https://www.bosterbio.com/catalog/product/view/id/1285342026-03-10T04:39:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-3-sds-page.jpgAnti-Integrin b2 / ITGB2 / CD18 Reference Antibody (erlizumab)Anti-Integrin b2/ITGB2/CD18 Reference Antibody (erlizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-3-sec-hplc.jpgAnti-Integrin b2 / ITGB2 / CD18 Reference Antibody (erlizumab)The purity of Anti-Integrin b2/ITGB2/CD18 Reference Antibody (erlizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285352026-03-10T04:39:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-4-sds-page.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (ruplizumab)Anti-TNFSF5/CD40L/CD154 Reference Antibody (ruplizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-4-sec-hplc.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (ruplizumab)The purity of Anti-TNFSF5/CD40L/CD154 Reference Antibody (ruplizumab)is more than 99% https://www.bosterbio.com/catalog/product/view/id/1285362026-03-10T04:39:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-5-sds-page.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (dapirolizumab)Anti-TNFSF5/CD40L/CD154 Reference Antibody (dapirolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-5-sec-hplc.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (dapirolizumab)The purity of Anti-TNFSF5/CD40L/CD154 Reference Antibody (dapirolizumab)is more than 99.24% https://www.bosterbio.com/catalog/product/view/id/1285372026-03-10T04:39:06+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-6-sds-page.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (letolizumab)Anti-TNFSF5/CD40L/CD154 Reference Antibody (letolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-6-sec-hplc.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (letolizumab)The purity of Anti-TNFSF5/CD40L/CD154 Reference Antibody (letolizumab)is more than 98.32% https://www.bosterbio.com/catalog/product/view/id/1285382026-03-10T04:39:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-7-sds-page.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (Toralizumab)Anti-TNFSF5/CD40L/CD154 Reference Antibody (Toralizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01114-7-sec-hplc.jpgAnti-TNFSF5 / CD40L / CD154 Reference Antibody (Toralizumab)The purity of Anti-TNFSF5/CD40L/CD154 Reference Antibody (Toralizumab)is more than 99.51% https://www.bosterbio.com/catalog/product/view/id/1285392026-03-10T04:39:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01134-1-sds-page.jpgAnti-Complement Factor D Reference Antibody (lampalizumab)Anti-Complement Factor D Reference Antibody (lampalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01134-1-sec-hplc.jpgAnti-Complement Factor D Reference Antibody (lampalizumab)The purity of Anti-Complement Factor D Reference Antibody (lampalizumab)is more than 99.38%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01134-1-od450.jpgAnti-Complement Factor D Reference Antibody (lampalizumab)Immobilized human Complement Factor D https://www.bosterbio.com/catalog/product/view/id/1285402026-03-10T04:39:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01144-3-sds-page.jpgAnti-IL-1a & IL1b Reference Antibody (Lutikizumab)Anti-IL-1a & IL1b Reference Antibody (Lutikizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01144-3-sec-hplc.jpgAnti-IL-1a & IL1b Reference Antibody (Lutikizumab)The purity of Anti-IL-1a & IL1b Reference Antibody (Lutikizumab)is more than 98.44%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01144-3-od450.jpgAnti-IL-1a & IL1b Reference Antibody (Lutikizumab)Immobilized human IL 1a https://www.bosterbio.com/catalog/product/view/id/1285412026-03-10T04:39:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01144-4-sds-page.jpgAnti-IL-1a Reference Antibody (bermekimab)Anti-IL-1a Reference Antibody (bermekimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01144-4-sec-hplc.jpgAnti-IL-1a Reference Antibody (bermekimab)The purity of Anti-IL-1a Reference Antibody (bermekimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285422026-03-10T04:39:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01147-sds-page.jpgAnti-ANGPTL4 Reference Antibody (Nanyang Tech.U. patent anti-ANGPTL4)Anti-ANGPTL4 Reference Antibody (Nanyang Tech.U. patent anti-ANGPTL4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01147-sec-hplc.jpgAnti-ANGPTL4 Reference Antibody (Nanyang Tech.U. patent anti-ANGPTL4)The purity of Anti-ANGPTL4 Reference Antibody (Nanyang Tech.U. patent anti-ANGPTL4)is more than 98.6% https://www.bosterbio.com/catalog/product/view/id/1285432026-03-10T04:39:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01148-4-sds-page.jpgAnti-TNFRSF7 / CD27 Reference Antibody (varlilumab)Anti-TNFRSF7/CD27 Reference Antibody (varlilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01148-4-sec-hplc.jpgAnti-TNFRSF7 / CD27 Reference Antibody (varlilumab)The purity of Anti-TNFRSF7/CD27 Reference Antibody (varlilumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01148-4-od450.jpgAnti-TNFRSF7 / CD27 Reference Antibody (varlilumab)Immobilized human CD27 FC at 2 &mug/mL can bind Anti-TNFRSF7/CD27 Reference Antibody (varlilumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01148-4-facs.jpgAnti-TNFRSF7 / CD27 Reference Antibody (varlilumab)HumanCD27 HEK293 cells were stained with Anti-TNFRSF7/CD27 Reference Antibody (varlilumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1285442026-03-10T04:39:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01148-5-sds-page.jpgAnti-TNFRSF7 / CD27 Reference Antibody (Organon patent anti-CD27)Anti-TNFRSF7/CD27 Reference Antibody (Organon patent anti-CD27) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01148-5-sec-hplc.jpgAnti-TNFRSF7 / CD27 Reference Antibody (Organon patent anti-CD27)The purity of Anti-TNFRSF7/CD27 Reference Antibody (Organon patent anti-CD27)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285452026-03-10T04:39:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01152-4-sds-page.jpgAnti-IL-12b Reference Antibody (ebdarokimab)Anti-IL-12b Reference Antibody (ebdarokimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01152-4-sec-hplc.jpgAnti-IL-12b Reference Antibody (ebdarokimab)The purity of Anti-IL-12b Reference Antibody (ebdarokimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01152-4-od450.jpgAnti-IL-12b Reference Antibody (ebdarokimab)Immobilized human IL-12b His at 2 &mug/mL can bind Anti-IL-12b Reference Antibody (ebdarokimab) https://www.bosterbio.com/catalog/product/view/id/1285462026-03-10T04:39:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01189-2-sds-page.jpgAnti-CD36 Reference Antibody (Ona Thera Patent Anti-Cd36)Anti-CD36 Reference Antibody (Ona Thera Patent Anti-Cd36) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01189-2-sec-hplc.jpgAnti-CD36 Reference Antibody (Ona Thera Patent Anti-Cd36)The purity of Anti-CD36 Reference Antibody (Ona Thera Patent Anti-Cd36)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285472026-03-10T04:39:08+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01191-1-sds-page.jpgAnti-FGF19 Reference Antibody (1A6)Anti-FGF19 Reference Antibody (1A6) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01191-1-sec-hplc.jpgAnti-FGF19 Reference Antibody (1A6)The purity of Anti-FGF19 Reference Antibody (1A6)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285482026-03-10T04:39:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-5-sds-page.jpgAnti-HLA-DR Reference Antibody (IMMU-114)Anti-HLA-DR Reference Antibody (IMMU-114) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01195-5-sec-hplc.jpgAnti-HLA-DR Reference Antibody (IMMU-114)The purity of Anti-HLA-DR Reference Antibody (IMMU-114)is more than 98.76% https://www.bosterbio.com/catalog/product/view/id/1285492026-03-10T04:39:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01196-4-sds-page.jpgAnti-PRLR / Prolactin Receptor Reference Antibody (rolinsatamab)Anti-PRLR/Prolactin Receptor Reference Antibody (rolinsatamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01196-4-sec-hplc.jpgAnti-PRLR / Prolactin Receptor Reference Antibody (rolinsatamab)The purity of Anti-PRLR/Prolactin Receptor Reference Antibody (rolinsatamab)is more than 91.67% https://www.bosterbio.com/catalog/product/view/id/1285502026-03-10T04:39:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01196-5-sds-page.jpgAnti-PRLR / Prolactin Receptor Reference Antibody (BAY 1158061)Anti-PRLR/Prolactin Receptor Reference Antibody (BAY 1158061) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01196-5-sec-hplc.jpgAnti-PRLR / Prolactin Receptor Reference Antibody (BAY 1158061)The purity of Anti-PRLR/Prolactin Receptor Reference Antibody (BAY 1158061)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285512026-03-10T04:39:09+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01199-3-sds-page.jpgAnti-VCAM1 / CD106 Reference Antibody (Hanwha patent anti-VCAM-1)Anti-VCAM1/CD106 Reference Antibody (Hanwha patent anti-VCAM-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01199-3-sec-hplc.jpgAnti-VCAM1 / CD106 Reference Antibody (Hanwha patent anti-VCAM-1)The purity of Anti-VCAM1/CD106 Reference Antibody (Hanwha patent anti-VCAM-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285522026-03-10T04:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-1-sds-page.jpgAnti-CD9 Reference Antibody (Genentech patent anti-CD9)Anti-CD9 Reference Antibody (Genentech patent anti-CD9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01202-1-sec-hplc.jpgAnti-CD9 Reference Antibody (Genentech patent anti-CD9)The purity of Anti-CD9 Reference Antibody (Genentech patent anti-CD9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285532026-03-10T04:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-2-sds-page.jpgAnti-S100A4 Reference Antibody (LK-1)Anti-S100A4 Reference Antibody (LK-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01217-2-sec-hplc.jpgAnti-S100A4 Reference Antibody (LK-1)The purity of Anti-S100A4 Reference Antibody (LK-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285542026-03-10T04:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01225-4-sds-page.jpgAnti-TNFRSF8 / CD30 Reference Antibody (brentuximab vedotin)Anti-TNFRSF8/CD30 Reference Antibody (brentuximab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01225-4-sec-hplc.jpgAnti-TNFRSF8 / CD30 Reference Antibody (brentuximab vedotin)The purity of Anti-TNFRSF8/CD30 Reference Antibody (brentuximab vedotin)is more than 98.99%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01225-4-od450.jpgAnti-TNFRSF8 / CD30 Reference Antibody (brentuximab vedotin)Immobilized human CD30 His at 2 &mug/mL can bind Anti-TNFRSF8/CD30 Reference Antibody (brentuximab vedotin) https://www.bosterbio.com/catalog/product/view/id/1285552026-03-10T04:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01225-5-sds-page.jpgAnti-TNFRSF8 / CD30 Reference Antibody (brentuximab)Anti-TNFRSF8/CD30 Reference Antibody (brentuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01225-5-sec-hplc.jpgAnti-TNFRSF8 / CD30 Reference Antibody (brentuximab)The purity of Anti-TNFRSF8/CD30 Reference Antibody (brentuximab)is more than 98.99%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01225-5-od450.jpgAnti-TNFRSF8 / CD30 Reference Antibody (brentuximab)Immobilized human CD30 His at 2 &mug/mL can bind Anti-TNFRSF8/CD30 Reference Antibody (brentuximab) https://www.bosterbio.com/catalog/product/view/id/1285562026-03-10T04:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01226-2-sds-page.jpgAnti-F12 / Factor XII Reference Antibody (garadacimab)Anti-F12/Factor XII Reference Antibody (garadacimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01226-2-sec-hplc.jpgAnti-F12 / Factor XII Reference Antibody (garadacimab)The purity of Anti-F12/Factor XII Reference Antibody (garadacimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1285572026-03-10T04:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01245-3-sds-page.jpgAnti-Albumin Reference Antibody (Numab patent anti-HSA)Anti-Albumin Reference Antibody (Numab patent anti-HSA) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01245-3-sec-hplc.jpgAnti-Albumin Reference Antibody (Numab patent anti-HSA)The purity of Anti-Albumin Reference Antibody (Numab patent anti-HSA)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285582026-03-10T04:39:10+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01257-2-sds-page.jpgAnti-TNFSF13B / BAFF / CD257 Reference Antibody (tabalumab)Anti-TNFSF13B/BAFF/CD257 Reference Antibody (tabalumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01257-2-sec-hplc.jpgAnti-TNFSF13B / BAFF / CD257 Reference Antibody (tabalumab)The purity of Anti-TNFSF13B/BAFF/CD257 Reference Antibody (tabalumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285592026-03-10T04:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01257-3-sds-page.jpgAnti-TNFSF13B / BAFF / CD257 Reference Antibody (belimumab)Anti-TNFSF13B/BAFF/CD257 Reference Antibody (belimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01257-3-sec-hplc.jpgAnti-TNFSF13B / BAFF / CD257 Reference Antibody (belimumab)The purity of Anti-TNFSF13B/BAFF/CD257 Reference Antibody (belimumab)is more than 97% https://www.bosterbio.com/catalog/product/view/id/1285602026-03-10T04:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01260-1-sds-page.jpgAnti-Complement Factor B Reference Antibody (Genentech patent anti-Factor B)Anti-Complement Factor B Reference Antibody (Genentech patent anti-Factor B) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01260-1-sec-hplc.jpgAnti-Complement Factor B Reference Antibody (Genentech patent anti-Factor B)The purity of Anti-Complement Factor B Reference Antibody (Genentech patent anti-Factor B)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285612026-03-10T04:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01262-4-sds-page.jpgAnti-PMEL Reference Antibody (Genentech anti-PMEL17)Anti-PMEL Reference Antibody (Genentech anti-PMEL17) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01262-4-sec-hplc.jpgAnti-PMEL Reference Antibody (Genentech anti-PMEL17)The purity of Anti-PMEL Reference Antibody (Genentech anti-PMEL17)is more than 99.73% https://www.bosterbio.com/catalog/product/view/id/1285622026-03-10T04:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01262-5-sds-page.jpgAnti-PMEL Reference Antibody (Novartis patent anti-PMEL17)Anti-PMEL Reference Antibody (Novartis patent anti-PMEL17) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01262-5-sec-hplc.jpgAnti-PMEL Reference Antibody (Novartis patent anti-PMEL17)The purity of Anti-PMEL Reference Antibody (Novartis patent anti-PMEL17)is more than 96.2% https://www.bosterbio.com/catalog/product/view/id/1285632026-03-10T04:39:11+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01264-sds-page.jpgAnti-LAP Reference Antibody (Brigham and Womens anti-LAP)Anti-LAP Reference Antibody (Brigham and Womens anti-LAP) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01264-sec-hplc.jpgAnti-LAP Reference Antibody (Brigham and Womens anti-LAP)The purity of Anti-LAP Reference Antibody (Brigham and Womens anti-LAP)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285642026-03-10T04:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01274-sds-page.jpgAnti-TIE2 / CD202b Reference Antibody (Regeneron patent anti-TIE-2)Anti-TIE2/CD202b Reference Antibody (Regeneron patent anti-TIE-2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01274-sec-hplc.jpgAnti-TIE2 / CD202b Reference Antibody (Regeneron patent anti-TIE-2)The purity of Anti-TIE2/CD202b Reference Antibody (Regeneron patent anti-TIE-2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285652026-03-10T04:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01276-2-sds-page.jpgAnti-VEGFR3 / FLT4 Reference Antibody (LY3022856)Anti-VEGFR3/FLT4 Reference Antibody (LY3022856) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01276-2-sec-hplc.jpgAnti-VEGFR3 / FLT4 Reference Antibody (LY3022856)The purity of Anti-VEGFR3/FLT4 Reference Antibody (LY3022856)is more than 98.74% https://www.bosterbio.com/catalog/product/view/id/1285662026-03-10T04:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01283-sds-page.jpgAnti-CHI3L1 Reference Antibody (Brown U. patent anti-CHI3L1)Anti-CHI3L1 Reference Antibody (Brown U. patent anti-CHI3L1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01283-sec-hplc.jpgAnti-CHI3L1 Reference Antibody (Brown U. patent anti-CHI3L1)The purity of Anti-CHI3L1 Reference Antibody (Brown U. patent anti-CHI3L1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285672026-03-10T04:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01311-1-sds-page.jpgAnti-IL-17Ra / CD217 Reference Antibody (brodalumab)Anti-IL-17Ra/CD217 Reference Antibody (brodalumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01311-1-sec-hplc.jpgAnti-IL-17Ra / CD217 Reference Antibody (brodalumab)The purity of Anti-IL-17Ra/CD217 Reference Antibody (brodalumab)is more than 99.05% https://www.bosterbio.com/catalog/product/view/id/1285682026-03-10T04:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-3-sds-page.jpgAnti-NRP1 / VEGF165R / CD304 Reference Antibody (vesencumab)Anti-NRP1/VEGF165R/CD304 Reference Antibody (vesencumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-3-sec-hplc.jpgAnti-NRP1 / VEGF165R / CD304 Reference Antibody (vesencumab)The purity of Anti-NRP1/VEGF165R/CD304 Reference Antibody (vesencumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-3-od450.jpgAnti-NRP1 / VEGF165R / CD304 Reference Antibody (vesencumab)Immobilized human NRP1 His at 2 &mug/mL can bind Anti-NRP1/VEGF165R/CD304 Reference Antibody (vesencumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01324-3-facs.jpgAnti-NRP1 / VEGF165R / CD304 Reference Antibody (vesencumab)Human NRP1 HEK293 cells were stained with Anti-NRP1/VEGF165R/CD304 Reference Antibody (vesencumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1285692026-03-10T04:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01330-sds-page.jpgAnti-MICB Reference Antibody (U.Washington patent anti-MICB)Anti-MICB Reference Antibody (U.Washington patent anti-MICB) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01330-sec-hplc.jpgAnti-MICB Reference Antibody (U.Washington patent anti-MICB)The purity of Anti-MICB Reference Antibody (U.Washington patent anti-MICB)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285702026-03-10T04:39:12+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-6-sds-page.jpgAnti-SCFR / c-Kit / CD117 Reference Antibody (Barzolvolimab)Anti-SCFR/c-Kit/CD117 Reference Antibody (Barzolvolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-6-sec-hplc.jpgAnti-SCFR / c-Kit / CD117 Reference Antibody (Barzolvolimab)The purity of Anti-SCFR/c-Kit/CD117 Reference Antibody (Barzolvolimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1285712026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-7-sds-page.jpgAnti-SCFR / c-Kit / CD117 Reference Antibody (CDX-0158)Anti-SCFR/c-Kit/CD117 Reference Antibody (CDX-0158) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-7-sec-hplc.jpgAnti-SCFR / c-Kit / CD117 Reference Antibody (CDX-0158)The purity of Anti-SCFR/c-Kit/CD117 Reference Antibody (CDX-0158)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285722026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-8-sds-page.jpgAnti-SCFR / c-Kit / CD117 Reference Antibody (LOP628)Anti-SCFR/c-Kit/CD117 Reference Antibody (LOP628) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01335-8-sec-hplc.jpgAnti-SCFR / c-Kit / CD117 Reference Antibody (LOP628)The purity of Anti-SCFR/c-Kit/CD117 Reference Antibody (LOP628)is more than 98.4% https://www.bosterbio.com/catalog/product/view/id/1285732026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-4-sds-page.jpgAnti-CD74 Reference Antibody (milatuzumab)Anti-CD74 Reference Antibody (milatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01340-4-sec-hplc.jpgAnti-CD74 Reference Antibody (milatuzumab)The purity of Anti-CD74 Reference Antibody (milatuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1285742026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01347-2-sds-page.jpgAnti-Hepcidin / HAMP Reference Antibody (LY2787106)Anti-Hepcidin/HAMP Reference Antibody (LY2787106) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01347-2-sec-hplc.jpgAnti-Hepcidin / HAMP Reference Antibody (LY2787106)The purity of Anti-Hepcidin/HAMP Reference Antibody (LY2787106)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285752026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01347-3-sds-page.jpgAnti-Hepcidin / HAMP Reference Antibody (Ludwig-Maximilians U. anti_Hepsin)Anti-Hepcidin/HAMP Reference Antibody (Ludwig-Maximilians U. anti_Hepsin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01347-3-sec-hplc.jpgAnti-Hepcidin / HAMP Reference Antibody (Ludwig-Maximilians U. anti_Hepsin)The purity of Anti-Hepcidin/HAMP Reference Antibody (Ludwig-Maximilians U. anti_Hepsin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285762026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01362-1-sds-page.jpgAnti-Amyloid Alpha Reference Antibody (birtamimab)Anti-Amyloid Alpha Reference Antibody (birtamimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01362-1-sec-hplc.jpgAnti-Amyloid Alpha Reference Antibody (birtamimab)The purity of Anti-Amyloid Alpha Reference Antibody (birtamimab)is more than 99.11% https://www.bosterbio.com/catalog/product/view/id/1285772026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01366-1-sds-page.jpgAnti-MICA Reference Antibody (CLN-619)Anti-MICA Reference Antibody (CLN-619) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01366-1-sec-hplc.jpgAnti-MICA Reference Antibody (CLN-619)The purity of Anti-MICA Reference Antibody (CLN-619)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285782026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01388-4-sds-page.jpgAnti-TrkB / NTRK2 Reference Antibody (Rinat patent anti-TrkB)Anti-TrkB/NTRK2 Reference Antibody (Rinat patent anti-TrkB) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01388-4-sec-hplc.jpgAnti-TrkB / NTRK2 Reference Antibody (Rinat patent anti-TrkB)The purity of Anti-TrkB/NTRK2 Reference Antibody (Rinat patent anti-TrkB)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285792026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01397-sds-page.jpgAnti-CXCL9 Reference Antibody (Novimmune patent anti-CXCL9)Anti-CXCL9 Reference Antibody (Novimmune patent anti-CXCL9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01397-sec-hplc.jpgAnti-CXCL9 Reference Antibody (Novimmune patent anti-CXCL9)The purity of Anti-CXCL9 Reference Antibody (Novimmune patent anti-CXCL9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285802026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-4-sds-page.jpgAnti-CD79b Reference Antibody (polatuzumab)Anti-CD79b Reference Antibody (polatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-4-sec-hplc.jpgAnti-CD79b Reference Antibody (polatuzumab)The purity of Anti-CD79b Reference Antibody (polatuzumab)is more than 98.12%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-4-od450.jpgAnti-CD79b Reference Antibody (polatuzumab)Immobilized human CD79b His at16 &mug/mL can bind Anti-CD79b Reference Antibody (polatuzumab) https://www.bosterbio.com/catalog/product/view/id/1285812026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-5-sds-page.jpgAnti-CD79b Reference Antibody (polatuzumab vedotin-piiq)Anti-CD79b Reference Antibody (polatuzumab vedotin-piiq) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-5-sec-hplc.jpgAnti-CD79b Reference Antibody (polatuzumab vedotin-piiq)The purity of Anti-CD79b Reference Antibody (polatuzumab vedotin-piiq)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-5-od450.jpgAnti-CD79b Reference Antibody (polatuzumab vedotin-piiq)Immobilized human CD79b https://www.bosterbio.com/catalog/product/view/id/1285822026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-6-sds-page.jpgAnti-CD79b Reference Antibody (iladatuzumAb)Anti-CD79b Reference Antibody (iladatuzumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-6-sec-hplc.jpgAnti-CD79b Reference Antibody (iladatuzumAb)The purity of Anti-CD79b Reference Antibody (iladatuzumAb)is more than 99.3% https://www.bosterbio.com/catalog/product/view/id/1285832026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-7-sds-page.jpgAnti-CD79b Reference Antibody (Iladatuzumab vedotin)Anti-CD79b Reference Antibody (Iladatuzumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01399-7-sec-hplc.jpgAnti-CD79b Reference Antibody (Iladatuzumab vedotin)The purity of Anti-CD79b Reference Antibody (Iladatuzumab vedotin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285842026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01400-sds-page.jpgAnti-LIF Reference Antibody (MSC-1)Anti-LIF Reference Antibody (MSC-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01400-sec-hplc.jpgAnti-LIF Reference Antibody (MSC-1)The purity of Anti-LIF Reference Antibody (MSC-1)is more than 98.6%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01400-od450.jpgAnti-LIF Reference Antibody (MSC-1)Immobilized human LIF His at 2 &mug/mL can bind Anti-LIF Reference Antibody (MSC-1) https://www.bosterbio.com/catalog/product/view/id/1285852026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01408-3-sds-page.jpgAnti-FcgR3a / CD16a Reference Antibody (AFM13)Anti-FcgR3a/CD16a Reference Antibody (AFM13) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01408-3-sec-hplc.jpgAnti-FcgR3a / CD16a Reference Antibody (AFM13)The purity of Anti-FcgR3a/CD16a Reference Antibody (AFM13)is more than 99.55% https://www.bosterbio.com/catalog/product/view/id/1285862026-03-10T04:39:13+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-3-sds-page.jpgAnti-IL-6Ra / CD126 Reference Antibody (sarilumab)Anti-IL-6Ra/CD126 Reference Antibody (sarilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-3-sec-hplc.jpgAnti-IL-6Ra / CD126 Reference Antibody (sarilumab)The purity of Anti-IL-6Ra/CD126 Reference Antibody (sarilumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285872026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-4-sds-page.jpgAnti-IL-6Ra / CD126 Reference Antibody (levilimab)Anti-IL-6Ra/CD126 Reference Antibody (levilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-4-sec-hplc.jpgAnti-IL-6Ra / CD126 Reference Antibody (levilimab)The purity of Anti-IL-6Ra/CD126 Reference Antibody (levilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285882026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-5-sds-page.jpgAnti-IL-6Ra / CD126 Reference Antibody (APX007)Anti-IL-6Ra/CD126 Reference Antibody (APX007) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-5-sec-hplc.jpgAnti-IL-6Ra / CD126 Reference Antibody (APX007)The purity of Anti-IL-6Ra/CD126 Reference Antibody (APX007)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285892026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-6-sds-page.jpgAnti-IL-6Ra / CD126 Reference Antibody (sapelizumab)Anti-IL-6Ra/CD126 Reference Antibody (sapelizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01425-6-sec-hplc.jpgAnti-IL-6Ra / CD126 Reference Antibody (sapelizumab)The purity of Anti-IL-6Ra/CD126 Reference Antibody (sapelizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285902026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01450-3-sds-page.jpgAnti-FcgR2a / CD32a Reference Antibody (VIB9600)Anti-FcgR2a/CD32a Reference Antibody (VIB9600) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01450-3-sec-hplc.jpgAnti-FcgR2a / CD32a Reference Antibody (VIB9600)The purity of Anti-FcgR2a/CD32a Reference Antibody (VIB9600)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285912026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01468-2-sds-page.jpgAnti-ACVRL1 / ALK-1 Reference Antibody (ascrinvacumab)Anti-ACVRL1/ALK-1 Reference Antibody (ascrinvacumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01468-2-sec-hplc.jpgAnti-ACVRL1 / ALK-1 Reference Antibody (ascrinvacumab)The purity of Anti-ACVRL1/ALK-1 Reference Antibody (ascrinvacumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285922026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01474-sds-page.jpgAnti-SLC1A5 / ASCT2 Reference Antibody (idactamab)Anti-SLC1A5/ASCT2 Reference Antibody (idactamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01474-sec-hplc.jpgAnti-SLC1A5 / ASCT2 Reference Antibody (idactamab)The purity of Anti-SLC1A5/ASCT2 Reference Antibody (idactamab)is more than 99.15%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01474-od450.jpgAnti-SLC1A5 / ASCT2 Reference Antibody (idactamab)Immobilized human SLC1A5 293 VLP at16 &mug/mL can bind Anti-SLC1A5/ASCT2 Reference Antibody (idactamab) https://www.bosterbio.com/catalog/product/view/id/1285932026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-2-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (emibetuzumab)Anti-HGFR/c-Met Reference Antibody (emibetuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-2-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (emibetuzumab)The purity of Anti-HGFR/c-Met Reference Antibody (emibetuzumab)is more than 99.28%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-2-od450.jpgAnti-HGFR / c-Met Reference Antibody (emibetuzumab)Immobilized human c MET His at 2 &mug/mL can bind Anti-HGFR/c-Met Reference Antibody (emibetuzumab) https://www.bosterbio.com/catalog/product/view/id/1285942026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-3-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (amivantamab)Anti-HGFR/c-Met Reference Antibody (amivantamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-3-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (amivantamab)The purity of Anti-HGFR/c-Met Reference Antibody (amivantamab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-3-od450.jpgAnti-HGFR / c-Met Reference Antibody (amivantamab)Immobilized human cMet His at 2 &mug/mL can bind Anti-HGFR/c-Met Reference Antibody (amivantamab) https://www.bosterbio.com/catalog/product/view/id/1285952026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-4-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (telisotuzumab)Anti-HGFR/c-Met Reference Antibody (telisotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-4-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (telisotuzumab)The purity of Anti-HGFR/c-Met Reference Antibody (telisotuzumab)is more than 99.49%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-4-od450.jpgAnti-HGFR / c-Met Reference Antibody (telisotuzumab)Immobilized human cMet His at 2 &mug/mL can bind Anti-HGFR/c-Met Reference Antibody (telisotuzumab) https://www.bosterbio.com/catalog/product/view/id/1285962026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-5-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (telisotuzumab vedotin)Anti-HGFR/c-Met Reference Antibody (telisotuzumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-5-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (telisotuzumab vedotin)The purity of Anti-HGFR/c-Met Reference Antibody (telisotuzumab vedotin)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-5-od450.jpgAnti-HGFR / c-Met Reference Antibody (telisotuzumab vedotin)Immobilized human cMet His at 2 &mug/mL can bind Anti-HGFR/c-Met Reference Antibody (telisotuzumab vedotin) https://www.bosterbio.com/catalog/product/view/id/1285972026-03-10T04:39:14+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-6-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (onartuzumab)Anti-HGFR/c-Met Reference Antibody (onartuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-6-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (onartuzumab)The purity of Anti-HGFR/c-Met Reference Antibody (onartuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285982026-03-10T04:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-7-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (SAIT301)Anti-HGFR/c-Met Reference Antibody (SAIT301) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-7-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (SAIT301)The purity of Anti-HGFR/c-Met Reference Antibody (SAIT301)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1285992026-03-10T04:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-8-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (Korea RIBB patent anti-cMet)Anti-HGFR/c-Met Reference Antibody (Korea RIBB patent anti-cMet) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-8-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (Korea RIBB patent anti-cMet)The purity of Anti-HGFR/c-Met Reference Antibody (Korea RIBB patent anti-cMet)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286002026-03-10T04:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-9-sds-page.jpgAnti-HGFR / c-Met Reference Antibody (Metheresis patent anti-Met)Anti-HGFR/c-Met Reference Antibody (Metheresis patent anti-Met) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01488-9-sec-hplc.jpgAnti-HGFR / c-Met Reference Antibody (Metheresis patent anti-Met)The purity of Anti-HGFR/c-Met Reference Antibody (Metheresis patent anti-Met)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286012026-03-10T04:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01492-1-sds-page.jpgAnti-TRP1 / TYRP1 Reference Antibody (flanvotumab)Anti-TRP1/TYRP1 Reference Antibody (flanvotumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01492-1-sec-hplc.jpgAnti-TRP1 / TYRP1 Reference Antibody (flanvotumab)The purity of Anti-TRP1/TYRP1 Reference Antibody (flanvotumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286022026-03-10T04:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01507-1-sds-page.jpgAnti-EphB2 Reference Antibody (Genentech patent anti-EphB2)Anti-EphB2 Reference Antibody (Genentech patent anti-EphB2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01507-1-sec-hplc.jpgAnti-EphB2 Reference Antibody (Genentech patent anti-EphB2)The purity of Anti-EphB2 Reference Antibody (Genentech patent anti-EphB2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286032026-03-10T04:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-9-sds-page.jpgAnti-Siglec-3 / CD33 Reference Antibody (gemtuzumab-CLM)Anti-Siglec-3/CD33 Reference Antibody (gemtuzumab-CLM) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-9-sec-hplc.jpgAnti-Siglec-3 / CD33 Reference Antibody (gemtuzumab-CLM)The purity of Anti-Siglec-3/CD33 Reference Antibody (gemtuzumab-CLM)is more than 99.54%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-9-od450.jpgAnti-Siglec-3 / CD33 Reference Antibody (gemtuzumab-CLM)Immobilized human CD33 His at 2 &mug/mL can bind Anti-Siglec-3/CD33 Reference Antibody (gemtuzumab-CLM) https://www.bosterbio.com/catalog/product/view/id/1286042026-03-10T04:39:15+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-6-sds-page.jpgAnti-Siglec-3 / CD33 Reference Antibody (Gemtuzumab ozogamicin)Anti-Siglec-3/CD33 Reference Antibody (Gemtuzumab ozogamicin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-6-sec-hplc.jpgAnti-Siglec-3 / CD33 Reference Antibody (Gemtuzumab ozogamicin)The purity of Anti-Siglec-3/CD33 Reference Antibody (Gemtuzumab ozogamicin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286052026-03-10T04:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-7-sds-page.jpgAnti-Siglec-3 / CD33 Reference Antibody (IMGN779)Anti-Siglec-3/CD33 Reference Antibody (IMGN779) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-7-sec-hplc.jpgAnti-Siglec-3 / CD33 Reference Antibody (IMGN779)The purity of Anti-Siglec-3/CD33 Reference Antibody (IMGN779)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286062026-03-10T04:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-8-sds-page.jpgAnti-Siglec-3 / CD33 Reference Antibody (vadastuximab)Anti-Siglec-3/CD33 Reference Antibody (vadastuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-8-sec-hplc.jpgAnti-Siglec-3 / CD33 Reference Antibody (vadastuximab)The purity of Anti-Siglec-3/CD33 Reference Antibody (vadastuximab)is more than 99.23% https://www.bosterbio.com/catalog/product/view/id/1286072026-03-10T04:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-5-sds-page.jpgAnti-GDF8 / Myostatin Reference Antibody (domagrozumab)Anti-GDF8/Myostatin Reference Antibody (domagrozumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m00926-5-sec-hplc.jpgAnti-GDF8 / Myostatin Reference Antibody (domagrozumab)The purity of Anti-GDF8/Myostatin Reference Antibody (domagrozumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286082026-03-10T04:39:16+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-4-sds-page.jpgAnti-Siglec-3 / CD33 Reference Antibody (vadastuximab talirine)Anti-Siglec-3/CD33 Reference Antibody (vadastuximab talirine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01508-4-sec-hplc.jpgAnti-Siglec-3 / CD33 Reference Antibody (vadastuximab talirine)The purity of Anti-Siglec-3/CD33 Reference Antibody (vadastuximab talirine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286092026-03-10T04:39:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01512-1-sds-page.jpgAnti-CD200 Reference Antibody (samalizumab)Anti-CD200 Reference Antibody (samalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01512-1-sec-hplc.jpgAnti-CD200 Reference Antibody (samalizumab)The purity of Anti-CD200 Reference Antibody (samalizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286102026-03-10T04:39:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01530-sds-page.jpgAnti-ROBO1 Reference Antibody (Asclepius Technology patent anti-Robo1 CAR)Anti-ROBO1 Reference Antibody (Asclepius Technology patent anti-Robo1 CAR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01530-sec-hplc.jpgAnti-ROBO1 Reference Antibody (Asclepius Technology patent anti-Robo1 CAR)The purity of Anti-ROBO1 Reference Antibody (Asclepius Technology patent anti-Robo1 CAR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286112026-03-10T04:39:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-2-sds-page.jpgAnti-MSPR / RON / CD136 Reference Antibody (narnatumab)Anti-MSPR/RON/CD136 Reference Antibody (narnatumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-2-sec-hplc.jpgAnti-MSPR / RON / CD136 Reference Antibody (narnatumab)The purity of Anti-MSPR/RON/CD136 Reference Antibody (narnatumab)is more than 99.2% https://www.bosterbio.com/catalog/product/view/id/1286122026-03-10T04:39:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-3-sds-page.jpgAnti-MSPR / RON / CD136 Reference Antibody (H5B14)Anti-MSPR/RON/CD136 Reference Antibody (H5B14) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-3-sec-hplc.jpgAnti-MSPR / RON / CD136 Reference Antibody (H5B14)The purity of Anti-MSPR/RON/CD136 Reference Antibody (H5B14)is more than 99.53% https://www.bosterbio.com/catalog/product/view/id/1286132026-03-10T04:39:17+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-4-sds-page.jpgAnti-MSPR / RON / CD136 Reference Antibody (Aveo anti-RON)Anti-MSPR/RON/CD136 Reference Antibody (Aveo anti-RON) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-4-sec-hplc.jpgAnti-MSPR / RON / CD136 Reference Antibody (Aveo anti-RON)The purity of Anti-MSPR/RON/CD136 Reference Antibody (Aveo anti-RON)is more than 97.3%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01532-4-facs.jpgAnti-MSPR / RON / CD136 Reference Antibody (Aveo anti-RON)Hs746T cells were stained with Anti-MSPR/RON/CD136 Reference Antibody (Aveo anti-RON) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1286142026-03-10T04:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01534-sds-page.jpgAnti-CYR61 / CCN1 Reference Antibody (Roche patent anti-CCN1)Anti-CYR61/CCN1 Reference Antibody (Roche patent anti-CCN1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01534-sec-hplc.jpgAnti-CYR61 / CCN1 Reference Antibody (Roche patent anti-CCN1)The purity of Anti-CYR61/CCN1 Reference Antibody (Roche patent anti-CCN1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286152026-03-10T04:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-3-sds-page.jpgAnti-Integrin aVb3 (ITGAV & ITGB3) Reference Antibody (etaracizumab)Anti-Integrin aVb3 (ITGAV & ITGB3) Reference Antibody (etaracizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-3-sec-hplc.jpgAnti-Integrin aVb3 (ITGAV & ITGB3) Reference Antibody (etaracizumab)The purity of Anti-Integrin aVb3 (ITGAV & ITGB3) Reference Antibody (etaracizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286162026-03-10T04:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-4-sds-page.jpgAnti-Integrin aVb6 (ITGAV & ITGB6) Reference Antibody (STX-100)Anti-Integrin aVb6 (ITGAV & ITGB6) Reference Antibody (STX-100) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-4-sec-hplc.jpgAnti-Integrin aVb6 (ITGAV & ITGB6) Reference Antibody (STX-100)The purity of Anti-Integrin aVb6 (ITGAV & ITGB6) Reference Antibody (STX-100)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286172026-03-10T04:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-5-sds-page.jpgAnti-Integrin aV / ITGAV / CD51 Reference Antibody (abituzumab)Anti-Integrin aV/ITGAV/CD51 Reference Antibody (abituzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-5-sec-hplc.jpgAnti-Integrin aV / ITGAV / CD51 Reference Antibody (abituzumab)The purity of Anti-Integrin aV/ITGAV/CD51 Reference Antibody (abituzumab)is more than 98.44% https://www.bosterbio.com/catalog/product/view/id/1286182026-03-10T04:39:18+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-6-sds-page.jpgAnti-Integrin aV / ITGAV / CD51 Reference Antibody (intetumumab)Anti-Integrin aV/ITGAV/CD51 Reference Antibody (intetumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01561-6-sec-hplc.jpgAnti-Integrin aV / ITGAV / CD51 Reference Antibody (intetumumab)The purity of Anti-Integrin aV/ITGAV/CD51 Reference Antibody (intetumumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286192026-03-10T04:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-5-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (inotuzumab-MMAE)Anti-Siglec-2/CD22 Reference Antibody (inotuzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-5-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (inotuzumab-MMAE)The purity of Anti-Siglec-2/CD22 Reference Antibody (inotuzumab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286202026-03-10T04:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-6-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (pinatuzumab)Anti-Siglec-2/CD22 Reference Antibody (pinatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-6-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (pinatuzumab)The purity of Anti-Siglec-2/CD22 Reference Antibody (pinatuzumab)is more than 97.02%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-6-od450.jpgAnti-Siglec-2 / CD22 Reference Antibody (pinatuzumab)Immobilized human CD22 His at 2 &mug/mL can bind Anti-Siglec-2/CD22 Reference Antibody (pinatuzumab) https://www.bosterbio.com/catalog/product/view/id/1286212026-03-10T04:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-7-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (inotuzumab)Anti-Siglec-2/CD22 Reference Antibody (inotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-7-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (inotuzumab)The purity of Anti-Siglec-2/CD22 Reference Antibody (inotuzumab)is more than 96.81% https://www.bosterbio.com/catalog/product/view/id/1286222026-03-10T04:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-8-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (pinatuzumab vedotin)Anti-Siglec-2/CD22 Reference Antibody (pinatuzumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-8-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (pinatuzumab vedotin)The purity of Anti-Siglec-2/CD22 Reference Antibody (pinatuzumab vedotin)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-8-od450.jpgAnti-Siglec-2 / CD22 Reference Antibody (pinatuzumab vedotin)Immobilized human Siglec 2/CD22 https://www.bosterbio.com/catalog/product/view/id/1286232026-03-10T04:39:19+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-9-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (epratuzumab)Anti-Siglec-2/CD22 Reference Antibody (epratuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-9-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (epratuzumab)The purity of Anti-Siglec-2/CD22 Reference Antibody (epratuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286242026-03-10T04:39:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-10-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (moxetumomab)Anti-Siglec-2/CD22 Reference Antibody (moxetumomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-10-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (moxetumomab)The purity of Anti-Siglec-2/CD22 Reference Antibody (moxetumomab)is more than 96.1% https://www.bosterbio.com/catalog/product/view/id/1286252026-03-10T04:39:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-11-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (inotuzumab-CLM)Anti-Siglec-2/CD22 Reference Antibody (inotuzumab-CLM) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-11-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (inotuzumab-CLM)The purity of Anti-Siglec-2/CD22 Reference Antibody (inotuzumab-CLM)is more than 96.81% https://www.bosterbio.com/catalog/product/view/id/1286262026-03-10T04:39:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-12-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (NCI m971)Anti-Siglec-2/CD22 Reference Antibody (NCI m971) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-12-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (NCI m971)The purity of Anti-Siglec-2/CD22 Reference Antibody (NCI m971)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286272026-03-10T04:39:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-13-sds-page.jpgAnti-Siglec-2 / CD22 Reference Antibody (NCI m972)Anti-Siglec-2/CD22 Reference Antibody (NCI m972) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01572-13-sec-hplc.jpgAnti-Siglec-2 / CD22 Reference Antibody (NCI m972)The purity of Anti-Siglec-2/CD22 Reference Antibody (NCI m972)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286282026-03-10T04:39:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01583-2-sds-page.jpgAnti-GDF15 / MIC1 Reference Antibody (ponsegromab)Anti-GDF15/MIC1 Reference Antibody (ponsegromab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01583-2-sec-hplc.jpgAnti-GDF15 / MIC1 Reference Antibody (ponsegromab)The purity of Anti-GDF15/MIC1 Reference Antibody (ponsegromab)is more than 99.55%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01583-2-od450.jpgAnti-GDF15 / MIC1 Reference Antibody (ponsegromab)Immobilized human GDF15 His at 2 &mug/mL can bind Anti-GDF15/MIC1 Reference Antibody (ponsegromab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01583-2-proliferation-inhibiton-rate.jpgAnti-GDF15 / MIC1 Reference Antibody (ponsegromab)Anti-IL-6Ra/CD126 Reference Antibody (vobarilizumab) Proliferation inhibition using TF-1 Cell. The maximum proliferation inhibition rate is about 80%. https://www.bosterbio.com/catalog/product/view/id/1286292026-03-10T04:39:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01583-3-sds-page.jpgAnti-GDF15 / MIC1 Reference Antibody (CTL-002)Anti-GDF15/MIC1 Reference Antibody (CTL-002) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01583-3-sec-hplc.jpgAnti-GDF15 / MIC1 Reference Antibody (CTL-002)The purity of Anti-GDF15/MIC1 Reference Antibody (CTL-002)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286302026-03-10T04:39:20+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-2-sds-page.jpgAnti-MUC16 Reference Antibody (oregovomab)Anti-MUC16 Reference Antibody (oregovomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-2-sec-hplc.jpgAnti-MUC16 Reference Antibody (oregovomab)The purity of Anti-MUC16 Reference Antibody (oregovomab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286312026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-3-sds-page.jpgAnti-MUC16 Reference Antibody (Sofituzumab vedotin)Anti-MUC16 Reference Antibody (Sofituzumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-3-sec-hplc.jpgAnti-MUC16 Reference Antibody (Sofituzumab vedotin)The purity of Anti-MUC16 Reference Antibody (Sofituzumab vedotin)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286322026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-4-sds-page.jpgAnti-MUC16 Reference Antibody (abagovomab)Anti-MUC16 Reference Antibody (abagovomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-4-sec-hplc.jpgAnti-MUC16 Reference Antibody (abagovomab)The purity of Anti-MUC16 Reference Antibody (abagovomab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286332026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-5-sds-page.jpgAnti-MUC16 Reference Antibody (sofituzumab)Anti-MUC16 Reference Antibody (sofituzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-5-sec-hplc.jpgAnti-MUC16 Reference Antibody (sofituzumab)The purity of Anti-MUC16 Reference Antibody (sofituzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286342026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-6-sds-page.jpgAnti-MUC16 Reference Antibody (oregovomab-MMAE)Anti-MUC16 Reference Antibody (oregovomab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01641-6-sec-hplc.jpgAnti-MUC16 Reference Antibody (oregovomab-MMAE)The purity of Anti-MUC16 Reference Antibody (oregovomab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286352026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01666-2-sds-page.jpgAnti-Sortilin / SORT1 Reference Antibody (latozinemab)Anti-Sortilin/SORT1 Reference Antibody (latozinemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01666-2-sec-hplc.jpgAnti-Sortilin / SORT1 Reference Antibody (latozinemab)The purity of Anti-Sortilin/SORT1 Reference Antibody (latozinemab)is more than 96% https://www.bosterbio.com/catalog/product/view/id/1286362026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01683-6-sds-page.jpgAnti-MUC18 / MCAM / CD146 Reference Antibody (imaprelimab)Anti-MUC18/MCAM/CD146 Reference Antibody (imaprelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01683-6-sec-hplc.jpgAnti-MUC18 / MCAM / CD146 Reference Antibody (imaprelimab)The purity of Anti-MUC18/MCAM/CD146 Reference Antibody (imaprelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286372026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01711-sds-page.jpgAnti-PACAP38 Reference Antibody (Lilly patent anti-PACAP)Anti-PACAP38 Reference Antibody (Lilly patent anti-PACAP) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01711-sec-hplc.jpgAnti-PACAP38 Reference Antibody (Lilly patent anti-PACAP)The purity of Anti-PACAP38 Reference Antibody (Lilly patent anti-PACAP)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286382026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01718-5-sds-page.jpgAnti-ALP Reference Antibody (Seagen Patent Anti-Alpp)Anti-ALP Reference Antibody (Seagen Patent Anti-Alpp) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01718-5-sec-hplc.jpgAnti-ALP Reference Antibody (Seagen Patent Anti-Alpp)The purity of Anti-ALP Reference Antibody (Seagen Patent Anti-Alpp)is more than 97.51%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01718-5-od450.jpgAnti-ALP Reference Antibody (Seagen Patent Anti-Alpp)Immobilized human ALPP His at4 &mug/mL can bind Anti-ALP Reference Antibody (Seagen Patent Anti-Alpp) https://www.bosterbio.com/catalog/product/view/id/1286392026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01759-2-sds-page.jpgAnti-HBEGF Reference Antibody (U3-1565)Anti-HBEGF Reference Antibody (U3-1565) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01759-2-sec-hplc.jpgAnti-HBEGF Reference Antibody (U3-1565)The purity of Anti-HBEGF Reference Antibody (U3-1565)is more than 90.2% https://www.bosterbio.com/catalog/product/view/id/1286402026-03-10T04:39:21+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01759-3-sds-page.jpgAnti-HBEGF Reference Antibody (KHK2866)Anti-HBEGF Reference Antibody (KHK2866) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01759-3-sec-hplc.jpgAnti-HBEGF Reference Antibody (KHK2866)The purity of Anti-HBEGF Reference Antibody (KHK2866)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286412026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01767-6-sds-page.jpgAnti-PROM1 / CD133 Reference Antibody (Forerunner patent anti-Prominin-1)Anti-PROM1/CD133 Reference Antibody (Forerunner patent anti-Prominin-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01767-6-sec-hplc.jpgAnti-PROM1 / CD133 Reference Antibody (Forerunner patent anti-Prominin-1)The purity of Anti-PROM1/CD133 Reference Antibody (Forerunner patent anti-Prominin-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286422026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01777-2-sds-page.jpgAnti-CD83 Reference Antibody (Genentech patent anti-CD83)Anti-CD83 Reference Antibody (Genentech patent anti-CD83) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01777-2-sec-hplc.jpgAnti-CD83 Reference Antibody (Genentech patent anti-CD83)The purity of Anti-CD83 Reference Antibody (Genentech patent anti-CD83)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286432026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-2-sds-page.jpgAnti-ALCAM / CD166 Reference Antibody (praluzatamab)Anti-ALCAM/CD166 Reference Antibody (praluzatamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-2-sec-hplc.jpgAnti-ALCAM / CD166 Reference Antibody (praluzatamab)The purity of Anti-ALCAM/CD166 Reference Antibody (praluzatamab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-2-od450.jpgAnti-ALCAM / CD166 Reference Antibody (praluzatamab)Immobilized human ALCAM His at 2 &mug/mL can bind Anti-ALCAM/CD166 Reference Antibody (praluzatamab) https://www.bosterbio.com/catalog/product/view/id/1286442026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-3-sds-page.jpgAnti-ALCAM/CD166 Reference Antibody (praluzatamab ravtansine)Anti-ALCAM/CD166 Reference Antibody (praluzatamab ravtansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-3-sec-hplc.jpgAnti-ALCAM/CD166 Reference Antibody (praluzatamab ravtansine)The purity of Anti-ALCAM/CD166 Reference Antibody (praluzatamab ravtansine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286452026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-4-sds-page.jpgAnti-ALCAM / CD166 Reference Antibody (AT002)Anti-ALCAM/CD166 Reference Antibody (AT002) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-4-sec-hplc.jpgAnti-ALCAM / CD166 Reference Antibody (AT002)The purity of Anti-ALCAM/CD166 Reference Antibody (AT002)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286462026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-5-sds-page.jpgAnti-ALCAM/CD166 Reference Antibody (praluzatamab-MMAE)Anti-ALCAM/CD166 Reference Antibody (praluzatamab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01788-5-sec-hplc.jpgAnti-ALCAM/CD166 Reference Antibody (praluzatamab-MMAE)The purity of Anti-ALCAM/CD166 Reference Antibody (praluzatamab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286472026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01794-1-sds-page.jpgAnti-CD98 Reference Antibody (Ign523)Anti-CD98 Reference Antibody (Ign523) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01794-1-sec-hplc.jpgAnti-CD98 Reference Antibody (Ign523)The purity of Anti-CD98 Reference Antibody (Ign523)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01794-1-od450.jpgAnti-CD98 Reference Antibody (Ign523)Immobilized human CD98 His at0 can bind Anti-CD98 Reference Antibody (Ign523) https://www.bosterbio.com/catalog/product/view/id/1286482026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01794-2-sds-page.jpgAnti-CD98 Reference Antibody (KHK2898)Anti-CD98 Reference Antibody (KHK2898) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01794-2-sec-hplc.jpgAnti-CD98 Reference Antibody (KHK2898)The purity of Anti-CD98 Reference Antibody (KHK2898)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286492026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01801-1-sds-page.jpgAnti-HTRA1 Reference Antibody (Galegenimab)Anti-HTRA1 Reference Antibody (Galegenimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01801-1-sec-hplc.jpgAnti-HTRA1 Reference Antibody (Galegenimab)The purity of Anti-HTRA1 Reference Antibody (Galegenimab)is more than 99.72% https://www.bosterbio.com/catalog/product/view/id/1286502026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01801-2-sds-page.jpgAnti-HTRA1 Reference Antibody (FHTR2163)Anti-HTRA1 Reference Antibody (FHTR2163) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01801-2-sec-hplc.jpgAnti-HTRA1 Reference Antibody (FHTR2163)The purity of Anti-HTRA1 Reference Antibody (FHTR2163)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286512026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01804-1-sds-page.jpgAnti-RTN4 / NOGO Reference Antibody (ozanezumab)Anti-RTN4/NOGO Reference Antibody (ozanezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01804-1-sec-hplc.jpgAnti-RTN4 / NOGO Reference Antibody (ozanezumab)The purity of Anti-RTN4/NOGO Reference Antibody (ozanezumab)is more than 96.23% https://www.bosterbio.com/catalog/product/view/id/1286522026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01804-2-sds-page.jpgAnti-RTN4 / NOGO Reference Antibody (atinumab)Anti-RTN4/NOGO Reference Antibody (atinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01804-2-sec-hplc.jpgAnti-RTN4 / NOGO Reference Antibody (atinumab)The purity of Anti-RTN4/NOGO Reference Antibody (atinumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286532026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01840-3-sds-page.jpgAnti-ROR2 Reference Antibody (Ozuriftamab)Anti-ROR2 Reference Antibody (Ozuriftamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01840-3-sec-hplc.jpgAnti-ROR2 Reference Antibody (Ozuriftamab)The purity of Anti-ROR2 Reference Antibody (Ozuriftamab)is more than 99.73%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01840-3-od450.jpgAnti-ROR2 Reference Antibody (Ozuriftamab)Immobilized human ROR2 His at 2 &mug/mL can bind Anti-ROR2 Reference Antibody (Ozuriftamab) https://www.bosterbio.com/catalog/product/view/id/1286542026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01840-4-sds-page.jpgAnti-ROR2 Reference Antibody (ozuriftamab vedotin)Anti-ROR2 Reference Antibody (ozuriftamab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01840-4-sec-hplc.jpgAnti-ROR2 Reference Antibody (ozuriftamab vedotin)The purity of Anti-ROR2 Reference Antibody (ozuriftamab vedotin)is more than 99.74% https://www.bosterbio.com/catalog/product/view/id/1286552026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01844-2-sds-page.jpgAnti-RTN4 / NOGO Reference Antibody (NG-101)Anti-RTN4/NOGO Reference Antibody (NG-101) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01844-2-sec-hplc.jpgAnti-RTN4 / NOGO Reference Antibody (NG-101)The purity of Anti-RTN4/NOGO Reference Antibody (NG-101)is more than 98.24% https://www.bosterbio.com/catalog/product/view/id/1286562026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01854-sds-page.jpgAnti-GREM1 / Gremlin Reference Antibody (Ginisortamab)Anti-GREM1/Gremlin Reference Antibody (Ginisortamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01854-sec-hplc.jpgAnti-GREM1 / Gremlin Reference Antibody (Ginisortamab)The purity of Anti-GREM1/Gremlin Reference Antibody (Ginisortamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286572026-03-10T04:39:22+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01854-1-sds-page.jpgAnti-GREM1 / Gremlin Reference Antibody (Regeneron patent anti-GREM1)Anti-GREM1/Gremlin Reference Antibody (Regeneron patent anti-GREM1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01854-1-sec-hplc.jpgAnti-GREM1 / Gremlin Reference Antibody (Regeneron patent anti-GREM1)The purity of Anti-GREM1/Gremlin Reference Antibody (Regeneron patent anti-GREM1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286582026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01854-2-sds-page.jpgAnti-GREM1 / Gremlin Reference Antibody (UCB patent anti-Gremlin-1)Anti-GREM1/Gremlin Reference Antibody (UCB patent anti-Gremlin-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01854-2-sec-hplc.jpgAnti-GREM1 / Gremlin Reference Antibody (UCB patent anti-Gremlin-1)The purity of Anti-GREM1/Gremlin Reference Antibody (UCB patent anti-Gremlin-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286592026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01898-1-sds-page.jpgAnti-Complement C5aR1 Reference Antibody (avdoralimab)Anti-Complement C5aR1 Reference Antibody (avdoralimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01898-1-sec-hplc.jpgAnti-Complement C5aR1 Reference Antibody (avdoralimab)The purity of Anti-Complement C5aR1 Reference Antibody (avdoralimab)is more than 99.63%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01898-1-od450.jpgAnti-Complement C5aR1 Reference Antibody (avdoralimab)Immobilized human C5AR1 VLP at16 &mug/mL can bind Anti-Complement C5aR1 Reference Antibody (avdoralimab) https://www.bosterbio.com/catalog/product/view/id/1286602026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01898-2-sds-page.jpgAnti-Complement C5aR1 Reference Antibody (G2 patent anti-C5aR)Anti-Complement C5aR1 Reference Antibody (G2 patent anti-C5aR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01898-2-sec-hplc.jpgAnti-Complement C5aR1 Reference Antibody (G2 patent anti-C5aR)The purity of Anti-Complement C5aR1 Reference Antibody (G2 patent anti-C5aR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286612026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01898-3-sds-page.jpgAnti-Complement C5aR1 Reference Antibody (G2_anti-C5aR)Anti-Complement C5aR1 Reference Antibody (G2_anti-C5aR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01898-3-sec-hplc.jpgAnti-Complement C5aR1 Reference Antibody (G2_anti-C5aR)The purity of Anti-Complement C5aR1 Reference Antibody (G2_anti-C5aR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286622026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01911-3-sds-page.jpgAnti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (volociximab)Anti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (volociximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01911-3-sec-hplc.jpgAnti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (volociximab)The purity of Anti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (volociximab)is more than 94.51% https://www.bosterbio.com/catalog/product/view/id/1286632026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01911-4-sds-page.jpgAnti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (BMS patent anti-Integrin alpha5beta1)Anti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (BMS patent anti-Integrin alpha5beta1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01911-4-sec-hplc.jpgAnti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (BMS patent anti-Integrin alpha5beta1)The purity of Anti-Integrin a5b1 (ITGA5 & ITGB1) Reference Antibody (BMS patent anti-Integrin alpha5beta1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286642026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-2-sds-page.jpgAnti-GPC3 / Glypican-3 Reference Antibody (codrituzumab)Anti-GPC3/Glypican-3 Reference Antibody (codrituzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-2-sec-hplc.jpgAnti-GPC3 / Glypican-3 Reference Antibody (codrituzumab)The purity of Anti-GPC3/Glypican-3 Reference Antibody (codrituzumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-2-od450.jpgAnti-GPC3 / Glypican-3 Reference Antibody (codrituzumab)Immobilized human GPC3https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-2-facs.jpgAnti-GPC3 / Glypican-3 Reference Antibody (codrituzumab)Human GPC3 CHOS cells were stained with Anti-GPC3/Glypican-3 Reference Antibody (codrituzumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-2-killing-rate.jpgAnti-GPC3 / Glypican-3 Reference Antibody (codrituzumab)The endocytosis ratio codrituzumab by HuH-7 increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-2-lysis.jpgAnti-GPC3 / Glypican-3 Reference Antibody (codrituzumab)Anti-GPC3/Glypican-3 Reference Antibody (Codrituzumab)-induced ADCC activity was evaluated using human GPC3 CHOS Cell. The max Lysis rate was approximately 30%. https://www.bosterbio.com/catalog/product/view/id/1286652026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-3-sds-page.jpgAnti-GPC3 / Glypican-3 Reference Antibody (Codrituzumab-MMAE)Anti-GPC3/Glypican-3 Reference Antibody (Codrituzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-3-sec-hplc.jpgAnti-GPC3 / Glypican-3 Reference Antibody (Codrituzumab-MMAE)The purity of Anti-GPC3/Glypican-3 Reference Antibody (Codrituzumab-MMAE)is more than 99.73%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01922-3-cell-viability.jpgAnti-GPC3 / Glypican-3 Reference Antibody (Codrituzumab-MMAE)The killing ratio Codrituzumab-MMAE by HuH-7 increased with the increase of antibody concentration https://www.bosterbio.com/catalog/product/view/id/1286662026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-1-sds-page.jpgAnti-Integrin a2b3 (ITGA2 & ITGB3) Reference Antibody (tadocizumab)Anti-Integrin a2b3 (ITGA2 & ITGB3) Reference Antibody (tadocizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-1-sec-hplc.jpgAnti-Integrin a2b3 (ITGA2 & ITGB3) Reference Antibody (tadocizumab)The purity of Anti-Integrin a2b3 (ITGA2 & ITGB3) Reference Antibody (tadocizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286672026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-2-sds-page.jpgAnti-Integrin a2b1 (ITGA2 & ITGB1) Reference Antibody (vatelizumab)Anti-Integrin a2b1 (ITGA2 & ITGB1) Reference Antibody (vatelizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01933-2-sec-hplc.jpgAnti-Integrin a2b1 (ITGA2 & ITGB1) Reference Antibody (vatelizumab)The purity of Anti-Integrin a2b1 (ITGA2 & ITGB1) Reference Antibody (vatelizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286682026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01953-sds-page.jpgAnti-SLC40A1 Reference Antibody (LY2928057)Anti-SLC40A1 Reference Antibody (LY2928057) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01953-sec-hplc.jpgAnti-SLC40A1 Reference Antibody (LY2928057)The purity of Anti-SLC40A1 Reference Antibody (LY2928057)is more than 99.9% https://www.bosterbio.com/catalog/product/view/id/1286692026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01953-1-sds-page.jpgAnti-SLC40A1 Reference Antibody (Amgen patent anti-Ferroportin)Anti-SLC40A1 Reference Antibody (Amgen patent anti-Ferroportin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01953-1-sec-hplc.jpgAnti-SLC40A1 Reference Antibody (Amgen patent anti-Ferroportin)The purity of Anti-SLC40A1 Reference Antibody (Amgen patent anti-Ferroportin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286702026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01955-1-sds-page.jpgAnti-C1q Reference Antibody (ANX005)Anti-C1q Reference Antibody (ANX005) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01955-1-sec-hplc.jpgAnti-C1q Reference Antibody (ANX005)The purity of Anti-C1q Reference Antibody (ANX005)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286712026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-2-sds-page.jpgAnti-TIGIT Reference Antibody (tiragolumab)Anti-TIGIT Reference Antibody (tiragolumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-2-sec-hplc.jpgAnti-TIGIT Reference Antibody (tiragolumab)The purity of Anti-TIGIT Reference Antibody (tiragolumab)is more than 95.79%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-2-od450.jpgAnti-TIGIT Reference Antibody (tiragolumab)Immobilized human TIGIT His at 2 &mug/mL can bind Anti-TIGIT Reference Antibody (tiragolumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-2-facs.jpgAnti-TIGIT Reference Antibody (tiragolumab)Human TIGIT HEK293 cells were stained with Anti-TIGIT Reference Antibody (tiragolumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-2-luminescence-intensity.jpgAnti-TIGIT Reference Antibody (tiragolumab)Anti-TIGIT Reference Antibody (tiragolumab)-induced TIGIT Luciferase activity was evaluated using hu-TIGIT-CD226-NFAT-Jurkat https://www.bosterbio.com/catalog/product/view/id/1286722026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-3-sds-page.jpgAnti-TIGIT Reference Antibody (vibostolimab)Anti-TIGIT Reference Antibody (vibostolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-3-sec-hplc.jpgAnti-TIGIT Reference Antibody (vibostolimab)The purity of Anti-TIGIT Reference Antibody (vibostolimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-3-od450.jpgAnti-TIGIT Reference Antibody (vibostolimab)Immobilized human TIGIT His at 2 &mug/mL can bind Anti-TIGIT Reference Antibody (vibostolimab) https://www.bosterbio.com/catalog/product/view/id/1286732026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-4-sds-page.jpgAnti-TIGIT Reference Antibody (ociperlimab)Anti-TIGIT Reference Antibody (ociperlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-4-sec-hplc.jpgAnti-TIGIT Reference Antibody (ociperlimab)The purity of Anti-TIGIT Reference Antibody (ociperlimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286742026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-5-sds-page.jpgAnti-TIGIT Reference Antibody (etigilimab)Anti-TIGIT Reference Antibody (etigilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-5-sec-hplc.jpgAnti-TIGIT Reference Antibody (etigilimab)The purity of Anti-TIGIT Reference Antibody (etigilimab)is more than 95.22% https://www.bosterbio.com/catalog/product/view/id/1286752026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-6-sds-page.jpgAnti-TIGIT Reference Antibody (domvanalimab)Anti-TIGIT Reference Antibody (domvanalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01962-6-sec-hplc.jpgAnti-TIGIT Reference Antibody (domvanalimab)The purity of Anti-TIGIT Reference Antibody (domvanalimab)is more than 99.65% https://www.bosterbio.com/catalog/product/view/id/1286762026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01965-2-sds-page.jpgAnti-B7-H2 / ICOSL / CD275 Reference Antibody (prezalumab)Anti-B7-H2/ICOSL/CD275 Reference Antibody (prezalumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01965-2-sec-hplc.jpgAnti-B7-H2 / ICOSL / CD275 Reference Antibody (prezalumab)The purity of Anti-B7-H2/ICOSL/CD275 Reference Antibody (prezalumab)is more than 98.05%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01965-2-od450.jpgAnti-B7-H2 / ICOSL / CD275 Reference Antibody (prezalumab)Immobilized human B7 H2 His at 2 &mug/mL can bind Anti-B7-H2/ICOSL/CD275 Reference Antibody (prezalumab) https://www.bosterbio.com/catalog/product/view/id/1286772026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01974-3-sds-page.jpgAnti-CD7 Reference Antibody (grisnilimAb)Anti-CD7 Reference Antibody (grisnilimAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01974-3-sec-hplc.jpgAnti-CD7 Reference Antibody (grisnilimAb)The purity of Anti-CD7 Reference Antibody (grisnilimAb)is more than 94.62% https://www.bosterbio.com/catalog/product/view/id/1286782026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01974-4-sds-page.jpgAnti-CD7 Reference Antibody (Persongen patent anti-CD7)Anti-CD7 Reference Antibody (Persongen patent anti-CD7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01974-4-sec-hplc.jpgAnti-CD7 Reference Antibody (Persongen patent anti-CD7)The purity of Anti-CD7 Reference Antibody (Persongen patent anti-CD7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286792026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02009-1-sds-page.jpgAnti-TNFSF12 / TWEAK Reference Antibody (RO5458640)Anti-TNFSF12/TWEAK Reference Antibody (RO5458640) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02009-1-sec-hplc.jpgAnti-TNFSF12 / TWEAK Reference Antibody (RO5458640)The purity of Anti-TNFSF12/TWEAK Reference Antibody (RO5458640)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286802026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02057-4-sds-page.jpgAnti-C1s Reference Antibody (sutimlimab)Anti-C1s Reference Antibody (sutimlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02057-4-sec-hplc.jpgAnti-C1s Reference Antibody (sutimlimab)The purity of Anti-C1s Reference Antibody (sutimlimab)is more than 96.87%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02057-4-od450.jpgAnti-C1s Reference Antibody (sutimlimab)Immobilized human C1S His at 2 &mug/mL can bind Anti-C1s Reference Antibody (sutimlimab) https://www.bosterbio.com/catalog/product/view/id/1286812026-03-10T04:39:23+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02120-2-sds-page.jpgAnti-NT5E / CD73 Reference Antibody (oleclumab)Anti-NT5E/CD73 Reference Antibody (oleclumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02120-2-sec-hplc.jpgAnti-NT5E / CD73 Reference Antibody (oleclumab)The purity of Anti-NT5E/CD73 Reference Antibody (oleclumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286822026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02120-3-sds-page.jpgAnti-NT5E / CD73 Reference Antibody (uliledlimab)Anti-NT5E/CD73 Reference Antibody (uliledlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02120-3-sec-hplc.jpgAnti-NT5E / CD73 Reference Antibody (uliledlimab)The purity of Anti-NT5E/CD73 Reference Antibody (uliledlimab)is more than 98.34% https://www.bosterbio.com/catalog/product/view/id/1286832026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02120-4-sds-page.jpgAnti-NT5E / CD73 Reference Antibody (mupadolimab)Anti-NT5E/CD73 Reference Antibody (mupadolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95.7%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02120-4-sec-hplc.jpgAnti-NT5E / CD73 Reference Antibody (mupadolimab)The purity of Anti-NT5E/CD73 Reference Antibody (mupadolimab)is more than 99.58% https://www.bosterbio.com/catalog/product/view/id/1286842026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02135-sds-page.jpgAnti-TREM1 / CD354 Reference Antibody (PY159)Anti-TREM1/CD354 Reference Antibody (PY159) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02135-sec-hplc.jpgAnti-TREM1 / CD354 Reference Antibody (PY159)The purity of Anti-TREM1/CD354 Reference Antibody (PY159)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02135-od450.jpgAnti-TREM1 / CD354 Reference Antibody (PY159)Immobilized human TREM1 His at 2 &mug/mL can bind Anti-TREM1/CD354 Reference Antibody (PY159)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02135-facs.jpgAnti-TREM1 / CD354 Reference Antibody (PY159)Human TREM1 HEK293 cells were stained with Anti-TREM1/CD354 Reference Antibody (PY159) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02135-killing-rate.jpgAnti-TREM1 / CD354 Reference Antibody (PY159)The endocytosis ratio PY159 by hu-TREM1-HEK293 increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02135-il-8.jpgAnti-TREM1 / CD354 Reference Antibody (PY159)Anti-TREM1 Reference Antibody (PY159) Activation was evaluated using PBMC. The max induction fold was approximately 3.16 https://www.bosterbio.com/catalog/product/view/id/1286852026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02150-sds-page.jpgAnti-TREM2 Reference Antibody (Py314)Anti-TREM2 Reference Antibody (Py314) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02150-sec-hplc.jpgAnti-TREM2 Reference Antibody (Py314)The purity of Anti-TREM2 Reference Antibody (Py314)is more than 97.69%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02150-od450.jpgAnti-TREM2 Reference Antibody (Py314)Immobilized Ma TREM2 His at 2 &mug/mL can bind Anti-TREM2 Reference Antibody (Py314)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02150-facs.jpgAnti-TREM2 Reference Antibody (Py314)Hu_TREM2 CHO-K1 cells were stained with Anti-TREM2 Reference Antibody (Py314) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1286862026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02152-2-sds-page.jpgAnti-TNFRSF10A / TRAILR1 / CD261 Reference Antibody ( mapatumumab)Anti-TNFRSF10A/TRAILR1/CD261 Reference Antibody ( mapatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02152-2-sec-hplc.jpgAnti-TNFRSF10A / TRAILR1 / CD261 Reference Antibody ( mapatumumab)The purity of Anti-TNFRSF10A/TRAILR1/CD261 Reference Antibody ( mapatumumab)is more than 98.89% https://www.bosterbio.com/catalog/product/view/id/1286872026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02200-sds-page.jpgAnti-KIR Reference Antibody (lirilumab)Anti-KIR Reference Antibody (lirilumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02200-sec-hplc.jpgAnti-KIR Reference Antibody (lirilumab)The purity of Anti-KIR Reference Antibody (lirilumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286882026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02208-sds-page.jpgAnti-GP6 / Glycoprotein-6 Reference Antibody (glenzocimab)Anti-GP6/Glycoprotein-6 Reference Antibody (glenzocimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02208-sec-hplc.jpgAnti-GP6 / Glycoprotein-6 Reference Antibody (glenzocimab)The purity of Anti-GP6/Glycoprotein-6 Reference Antibody (glenzocimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1286892026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02219-2-sds-page.jpgAnti-CSF2Rb / CD131 Reference Antibody (CSL311)Anti-CSF2Rb/CD131 Reference Antibody (CSL311) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02219-2-sec-hplc.jpgAnti-CSF2Rb / CD131 Reference Antibody (CSL311)The purity of Anti-CSF2Rb/CD131 Reference Antibody (CSL311)is more than 98.34%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02219-2-od450.jpgAnti-CSF2Rb / CD131 Reference Antibody (CSL311)Immobilized human CSF2RB His at 2 &mug/mL can bind Anti-CSF2Rb/CD131 Reference Antibody (CSL311)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02219-2-facs.jpgAnti-CSF2Rb / CD131 Reference Antibody (CSL311)Human CSF2RB HEK293 cells were stained with Anti-CSF2Rb/CD131 Reference Antibody (CSL311) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02219-2-inhibition-of-growth.jpgAnti-CSF2Rb / CD131 Reference Antibody (CSL311)IL-3-mediated proliferation of TF-1 can be completely blocked by antibodies with an IC50 of 0.2109 nM.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02219-2-inhibition-of-growth-1.jpgAnti-CSF2Rb / CD131 Reference Antibody (CSL311)GM-CSF-mediated proliferation of TF-1 can be completely blocked by antibodies with an IC50 of 4.105 nM. https://www.bosterbio.com/catalog/product/view/id/1286902026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-4-sds-page.jpgAnti-B7-H3 / CD276 Reference Antibody (enoblituzumab)Anti-B7-H3/CD276 Reference Antibody (enoblituzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-4-sec-hplc.jpgAnti-B7-H3 / CD276 Reference Antibody (enoblituzumab)The purity of Anti-B7-H3/CD276 Reference Antibody (enoblituzumab)is more than 98.61%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-4-od450.jpgAnti-B7-H3 / CD276 Reference Antibody (enoblituzumab)Immobilized human B7H3 His at 2 &mug/mL can bind Anti-B7-H3/CD276 Reference Antibody (enoblituzumab) https://www.bosterbio.com/catalog/product/view/id/1286912026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-5-sds-page.jpgAnti-B7-H3 / CD276 Reference Antibody (Vobramitamab)Anti-B7-H3/CD276 Reference Antibody (Vobramitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-5-sec-hplc.jpgAnti-B7-H3 / CD276 Reference Antibody (Vobramitamab)The purity of Anti-B7-H3/CD276 Reference Antibody (Vobramitamab)is more than 98.95% https://www.bosterbio.com/catalog/product/view/id/1286922026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-6-sds-page.jpgAnti-B7-H3 / CD276 Reference Antibody (omburtamab)Anti-B7-H3/CD276 Reference Antibody (omburtamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-6-sec-hplc.jpgAnti-B7-H3 / CD276 Reference Antibody (omburtamab)The purity of Anti-B7-H3/CD276 Reference Antibody (omburtamab)is more than 97.23% https://www.bosterbio.com/catalog/product/view/id/1286932026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-7-sds-page.jpgAnti-B7-H3 / CD276 Reference Antibody (mirzotamAb)Anti-B7-H3/CD276 Reference Antibody (mirzotamAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-7-sec-hplc.jpgAnti-B7-H3 / CD276 Reference Antibody (mirzotamAb)The purity of Anti-B7-H3/CD276 Reference Antibody (mirzotamAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286942026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-8-sds-page.jpgAnti-B7-H3 / CD276 Reference Antibody (Trellis patent anti-B7-H3)Anti-B7-H3/CD276 Reference Antibody (Trellis patent anti-B7-H3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02220-8-sec-hplc.jpgAnti-B7-H3 / CD276 Reference Antibody (Trellis patent anti-B7-H3)The purity of Anti-B7-H3/CD276 Reference Antibody (Trellis patent anti-B7-H3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286952026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02222-1-sds-page.jpgAnti-IL-7Ra / CD127 Reference Antibody (lusvertikimab)Anti-IL-7Ra/CD127 Reference Antibody (lusvertikimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02222-1-sec-hplc.jpgAnti-IL-7Ra / CD127 Reference Antibody (lusvertikimab)The purity of Anti-IL-7Ra/CD127 Reference Antibody (lusvertikimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02222-1-od450.jpgAnti-IL-7Ra / CD127 Reference Antibody (lusvertikimab)Immobilized human IL 7Ra/CD127 His at 2 &mug/mL can bind Anti-IL-7Ra/CD127 Reference Antibody (lusvertikimab) https://www.bosterbio.com/catalog/product/view/id/1286962026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02222-2-sds-page.jpgAnti-IL-7Ra / CD127 Reference Antibody (PF-06342674)Anti-IL-7Ra/CD127 Reference Antibody (PF-06342674) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02222-2-sec-hplc.jpgAnti-IL-7Ra / CD127 Reference Antibody (PF-06342674)The purity of Anti-IL-7Ra/CD127 Reference Antibody (PF-06342674)is more than 99.69% https://www.bosterbio.com/catalog/product/view/id/1286972026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02229-2-sds-page.jpgAnti-TGM2 / Transglutaminase 2 Reference Antibody (zampilimab)Anti-TGM2/Transglutaminase 2 Reference Antibody (zampilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02229-2-sec-hplc.jpgAnti-TGM2 / Transglutaminase 2 Reference Antibody (zampilimab)The purity of Anti-TGM2/Transglutaminase 2 Reference Antibody (zampilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286982026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02250-1-sds-page.jpgAnti-Nogo Receptor / NgR Reference Antibody (Abbott patent anti-NGR)Anti-Nogo Receptor/NgR Reference Antibody (Abbott patent anti-NGR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02250-1-sec-hplc.jpgAnti-Nogo Receptor / NgR Reference Antibody (Abbott patent anti-NGR)The purity of Anti-Nogo Receptor/NgR Reference Antibody (Abbott patent anti-NGR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1286992026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-1-sds-page.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab)Anti-FOLR1/FRA Reference Antibody (mirvetuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-1-sec-hplc.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab)The purity of Anti-FOLR1/FRA Reference Antibody (mirvetuximab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-1-od450.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab)Immobilized human FRa His at 2 &mug/mL can bind Anti-FOLR1/FRA Reference Antibody (mirvetuximab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-1-facs.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab)SKOV3 cells were stained with Anti-FOLR1/FRA Reference Antibody (mirvetuximab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-1-internalization-rate.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab)The endocytosis ratio mirvetuximab by Human Fralpha HEK 293 increased with the increase of antibody concentration https://www.bosterbio.com/catalog/product/view/id/1287002026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-2-sds-page.jpgAnti-FOLR1 / FRA Reference Antibody (farletuzumab-MMAE)Anti-FOLR1/FRA Reference Antibody (farletuzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-2-sec-hplc.jpgAnti-FOLR1 / FRA Reference Antibody (farletuzumab-MMAE)The purity of Anti-FOLR1/FRA Reference Antibody (farletuzumab-MMAE)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-2-od450.jpgAnti-FOLR1 / FRA Reference Antibody (farletuzumab-MMAE)Immobilized human FRalpha His at 2 &mug/mL can bind Anti-FOLR1/FRA Reference Antibody (farletuzumab-MMAE) https://www.bosterbio.com/catalog/product/view/id/1287012026-03-10T04:39:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-3-sds-page.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab-MMAE)Anti-FOLR1/FRA Reference Antibody (farletuzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-3-sec-hplc.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab-MMAE)The purity of Anti-FOLR1/FRA Reference Antibody (mirvetuximab-MMAE)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-3-od450.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab-MMAE)Immobilized human FRalpha His at 2 &mug/mL can bind Anti-FOLR1/FRA Reference Antibody (mirvetuximab-MMAE) https://www.bosterbio.com/catalog/product/view/id/1287022026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-4-sds-page.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab-MMAE)Anti-FOLR1/FRA Reference Antibody (mirvetuximab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-4-sec-hplc.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab-MMAE)The purity of Anti-FOLR1/FRA Reference Antibody (mirvetuximab-MMAE)is more than 98.89%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-4-od450.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab-MMAE)Immobilized human FRalpha His at 2 &mug/mL can bind Anti-FOLR1/FRA Reference Antibody (mirvetuximab-MMAE) https://www.bosterbio.com/catalog/product/view/id/1287032026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-5-sds-page.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab soravtansine)Anti-FOLR1/FRA Reference Antibody (mirvetuximab soravtansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-5-sec-hplc.jpgAnti-FOLR1 / FRA Reference Antibody (mirvetuximab soravtansine)The purity of Anti-FOLR1/FRA Reference Antibody (mirvetuximab soravtansine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287042026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-6-sds-page.jpgAnti-FOLR1 / FRA Reference Antibody (farletuzumab)Anti-FOLR1/FRA Reference Antibody (farletuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-6-sec-hplc.jpgAnti-FOLR1 / FRA Reference Antibody (farletuzumab)The purity of Anti-FOLR1/FRA Reference Antibody (farletuzumab)is more than 95.5%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-6-facs.jpgAnti-FOLR1 / FRA Reference Antibody (farletuzumab)Cyno FRalpha HEK293 cells were stained with Anti-FOLR1/FRA Reference Antibody (farletuzumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-6-internalization-rate.jpgAnti-FOLR1 / FRA Reference Antibody (farletuzumab)The endocytosis ratio farletuzumab by Human Fralpha HEK 293 increased with the increase of antibody concentration https://www.bosterbio.com/catalog/product/view/id/1287052026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-7-sds-page.jpgAnti-FOLR1 / FRA Reference Antibody (Dompe patent anti-FOLR1)Anti-FOLR1/FRA Reference Antibody (Dompe patent anti-FOLR1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02254-7-sec-hplc.jpgAnti-FOLR1 / FRA Reference Antibody (Dompe patent anti-FOLR1)The purity of Anti-FOLR1/FRA Reference Antibody (Dompe patent anti-FOLR1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287062026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02268-1-sds-page.jpgAnti-AA2AR / Adenosine A2aR Reference Antibody (3F6-9G5)Anti-AA2AR/Adenosine A2aR Reference Antibody (3F6-9G5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02268-1-sec-hplc.jpgAnti-AA2AR / Adenosine A2aR Reference Antibody (3F6-9G5)The purity of Anti-AA2AR/Adenosine A2aR Reference Antibody (3F6-9G5)is more than 98.85%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02268-1-od450.jpgAnti-AA2AR / Adenosine A2aR Reference Antibody (3F6-9G5)Immobilized human A2aR VLP at 2 &mug/mL can bind Anti-AA2AR/Adenosine A2aR Reference Antibody (3F6-9G5) https://www.bosterbio.com/catalog/product/view/id/1287072026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02280-2-sds-page.jpgAnti-CSF3 / G-CSF Reference Antibody (CSL324)Anti-CSF3/G-CSF Reference Antibody (CSL324) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02280-2-sec-hplc.jpgAnti-CSF3 / G-CSF Reference Antibody (CSL324)The purity of Anti-CSF3/G-CSF Reference Antibody (CSL324)is more than 99.09% https://www.bosterbio.com/catalog/product/view/id/1287082026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02298-1-sds-page.jpgAnti-TNFSF14 / LIGHT / CD258 Reference Antibody (SAR252067)Anti-TNFSF14/LIGHT/CD258 Reference Antibody (SAR252067) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02298-1-sec-hplc.jpgAnti-TNFSF14 / LIGHT / CD258 Reference Antibody (SAR252067)The purity of Anti-TNFSF14/LIGHT/CD258 Reference Antibody (SAR252067)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287092026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02320-1-sds-page.jpgAnti-CD151 Reference Antibody (Pierre Fabre patent anti-CD151)Anti-CD151 Reference Antibody (Pierre Fabre patent anti-CD151) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02320-1-sec-hplc.jpgAnti-CD151 Reference Antibody (Pierre Fabre patent anti-CD151)The purity of Anti-CD151 Reference Antibody (Pierre Fabre patent anti-CD151)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287102026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02323-1-sds-page.jpgAnti-MASP2 Reference Antibody (narsoplimab)Anti-MASP2 Reference Antibody (narsoplimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02323-1-sec-hplc.jpgAnti-MASP2 Reference Antibody (narsoplimab)The purity of Anti-MASP2 Reference Antibody (narsoplimab)is more than 98.94%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02323-1-od450.jpgAnti-MASP2 Reference Antibody (narsoplimab)Immobilized human MASP 2A His at 2 &mug/mL can bind Anti-MASP2 Reference Antibody (narsoplimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02323-1-od405.jpgAnti-MASP2 Reference Antibody (narsoplimab)C5b-C9 of the MBL pathway can be completely inhibited by Anti-MASP2 Reference Antibody (narsoplimab) with an IC50 of 0.7337 &mug/mL. https://www.bosterbio.com/catalog/product/view/id/1287112026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02332-sds-page.jpgAnti-ASIC1 Reference Antibody (Regeneron patent anti-ASIC1)Anti-ASIC1 Reference Antibody (Regeneron patent anti-ASIC1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02332-sec-hplc.jpgAnti-ASIC1 Reference Antibody (Regeneron patent anti-ASIC1)The purity of Anti-ASIC1 Reference Antibody (Regeneron patent anti-ASIC1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287122026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02352-3-sds-page.jpgAnti-CALCA / CGRP Reference Antibody (eptinezumab)Anti-CALCA/CGRP Reference Antibody (eptinezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02352-3-sec-hplc.jpgAnti-CALCA / CGRP Reference Antibody (eptinezumab)The purity of Anti-CALCA/CGRP Reference Antibody (eptinezumab)is more than 95.91% https://www.bosterbio.com/catalog/product/view/id/1287132026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02352-4-sds-page.jpgAnti-CALCA / CGRP Reference Antibody (galcanezumab)Anti-CALCA/CGRP Reference Antibody (galcanezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02352-4-sec-hplc.jpgAnti-CALCA / CGRP Reference Antibody (galcanezumab)The purity of Anti-CALCA/CGRP Reference Antibody (galcanezumab)is more than 99.18% https://www.bosterbio.com/catalog/product/view/id/1287142026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02352-5-sds-page.jpgAnti-CALCA / CGRP Reference Antibody (fremanezumab)Anti-CALCA/CGRP Reference Antibody (fremanezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02352-5-sec-hplc.jpgAnti-CALCA / CGRP Reference Antibody (fremanezumab)The purity of Anti-CALCA/CGRP Reference Antibody (fremanezumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287152026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02411-3-sds-page.jpgAnti-CDCP1 / CD318 Reference Antibody (38 E11)Anti-CDCP1/CD318 Reference Antibody (38 E11) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02411-3-sec-hplc.jpgAnti-CDCP1 / CD318 Reference Antibody (38 E11)The purity of Anti-CDCP1/CD318 Reference Antibody (38 E11)is more than 95.48%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02411-3-od450.jpgAnti-CDCP1 / CD318 Reference Antibody (38 E11)Immobilized human CDCP1 His at 2 &mug/mL can bind Anti-CDCP1/CD318 Reference Antibody (38 E11) https://www.bosterbio.com/catalog/product/view/id/1287162026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02411-4-sds-page.jpgAnti-CDCP1 / CD318 Reference Antibody (U.California patent anti-CDCP1)Anti-CDCP1/CD318 Reference Antibody (U.California patent anti-CDCP1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02411-4-sec-hplc.jpgAnti-CDCP1 / CD318 Reference Antibody (U.California patent anti-CDCP1)The purity of Anti-CDCP1/CD318 Reference Antibody (U.California patent anti-CDCP1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287172026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02417-3-sds-page.jpgAnti-TNFSF13 / APRIL / CD256 Reference Antibody (sibeprenlimab)Anti-TNFSF13/APRIL/CD256 Reference Antibody (sibeprenlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02417-3-sec-hplc.jpgAnti-TNFSF13 / APRIL / CD256 Reference Antibody (sibeprenlimab)The purity of Anti-TNFSF13/APRIL/CD256 Reference Antibody (sibeprenlimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287182026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02417-4-sds-page.jpgAnti-TNFSF13 / APRIL / CD256 Reference Antibody (BION-1301)Anti-TNFSF13/APRIL/CD256 Reference Antibody (BION-1301) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02417-4-sec-hplc.jpgAnti-TNFSF13 / APRIL / CD256 Reference Antibody (BION-1301)The purity of Anti-TNFSF13/APRIL/CD256 Reference Antibody (BION-1301)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287192026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02428-2-sds-page.jpgAnti-Fc gamma R1 Reference Antibody (Medarex Patent Anti-Fc-Gamma-R1)Anti-Fc gamma R1 Reference Antibody (Medarex Patent Anti-Fc-Gamma-R1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02428-2-sec-hplc.jpgAnti-Fc gamma R1 Reference Antibody (Medarex Patent Anti-Fc-Gamma-R1)The purity of Anti-Fc gamma R1 Reference Antibody (Medarex Patent Anti-Fc-Gamma-R1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287202026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02439-2-sds-page.jpgAnti-GPNMB Reference Antibody (glembatumumab)Anti-GPNMB Reference Antibody (glembatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02439-2-sec-hplc.jpgAnti-GPNMB Reference Antibody (glembatumumab)The purity of Anti-GPNMB Reference Antibody (glembatumumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287212026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02439-3-sds-page.jpgAnti-GPNMB Reference Antibody (glembatumumab vedotin)Anti-GPNMB Reference Antibody (glembatumumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02439-3-sec-hplc.jpgAnti-GPNMB Reference Antibody (glembatumumab vedotin)The purity of Anti-GPNMB Reference Antibody (glembatumumab vedotin)is more than 99.7% https://www.bosterbio.com/catalog/product/view/id/1287222026-03-10T04:39:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02471-1-sds-page.jpgAnti-ANGPTL8 Reference Antibody (Regeneron patent anti-ANGPTL8)Anti-ANGPTL8 Reference Antibody (Regeneron patent anti-ANGPTL8) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02471-1-sec-hplc.jpgAnti-ANGPTL8 Reference Antibody (Regeneron patent anti-ANGPTL8)The purity of Anti-ANGPTL8 Reference Antibody (Regeneron patent anti-ANGPTL8)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287232026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-4-sds-page.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (cudarolimab)Anti-TNFRSF4/OX40/CD134 Reference Antibody (cudarolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-4-sec-hplc.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (cudarolimab)The purity of Anti-TNFRSF4/OX40/CD134 Reference Antibody (cudarolimab)is more than 99.38%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-4-od450.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (cudarolimab)Immobilized human TNFRSF4 His at 2 &mug/mL can bind Anti-TNFRSF4/OX40/CD134 Reference Antibody (cudarolimab) https://www.bosterbio.com/catalog/product/view/id/1287242026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-5-sds-page.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (tavolixizumab)Anti-TNFRSF4/OX40/CD134 Reference Antibody (tavolixizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-5-sec-hplc.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (tavolixizumab)The purity of Anti-TNFRSF4/OX40/CD134 Reference Antibody (tavolixizumab)is more than 97.98%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-5-od450.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (tavolixizumab)Immobilized human CD134 His at 2 &mug/mL can bind Anti-TNFRSF4/OX40/CD134 Reference Antibody (tavolixizumab) https://www.bosterbio.com/catalog/product/view/id/1287252026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-6-sds-page.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (revdofilimab)Anti-TNFRSF4/OX40/CD134 Reference Antibody (revdofilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-6-sec-hplc.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (revdofilimab)The purity of Anti-TNFRSF4/OX40/CD134 Reference Antibody (revdofilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287262026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-7-sds-page.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (telazorlimab)Anti-TNFRSF4/OX40/CD134 Reference Antibody (telazorlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-7-sec-hplc.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (telazorlimab)The purity of Anti-TNFRSF4/OX40/CD134 Reference Antibody (telazorlimab)is more than 96.11% https://www.bosterbio.com/catalog/product/view/id/1287272026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-8-sds-page.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (BMS-986178)Anti-TNFRSF4/OX40/CD134 Reference Antibody (BMS-986178) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-8-sec-hplc.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (BMS-986178)The purity of Anti-TNFRSF4/OX40/CD134 Reference Antibody (BMS-986178)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287282026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-9-sds-page.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (ivuxolimab)Anti-TNFRSF4/OX40/CD134 Reference Antibody (ivuxolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-9-sec-hplc.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (ivuxolimab)The purity of Anti-TNFRSF4/OX40/CD134 Reference Antibody (ivuxolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287292026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-10-sds-page.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (vonlerizumab)Anti-TNFRSF4/OX40/CD134 Reference Antibody (vonlerizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-10-sec-hplc.jpgAnti-TNFRSF4 / OX40 / CD134 Reference Antibody (vonlerizumab)The purity of Anti-TNFRSF4/OX40/CD134 Reference Antibody (vonlerizumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287302026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02497-sds-page.jpgAnti-LINGO1 Reference Antibody (opicinumab)Anti-LINGO1 Reference Antibody (opicinumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02497-sec-hplc.jpgAnti-LINGO1 Reference Antibody (opicinumab)The purity of Anti-LINGO1 Reference Antibody (opicinumab)is more than 99.03% https://www.bosterbio.com/catalog/product/view/id/1287312026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02512-2-sds-page.jpgAnti-SEMA4D / CD100 Reference Antibody (pepinemab)Anti-SEMA4D/CD100 Reference Antibody (pepinemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02512-2-sec-hplc.jpgAnti-SEMA4D / CD100 Reference Antibody (pepinemab)The purity of Anti-SEMA4D/CD100 Reference Antibody (pepinemab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02512-2-od450.jpgAnti-SEMA4D / CD100 Reference Antibody (pepinemab)Immobilized human SEMA4D/CD100https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02512-2-facs.jpgAnti-SEMA4D / CD100 Reference Antibody (pepinemab)Human C100 HEK293 cells were stained with Anti-SEMA4D/CD100 Reference Antibody (pepinemab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02512-2-syngeneic-ct-26-cell-model.jpgAnti-SEMA4D / CD100 Reference Antibody (pepinemab)Pepinemab inhibited the tumor growth of CT26 on balb/c mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1287322026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02514-1-sds-page.jpgAnti-CTSS / Cathepsin S Reference Antibody (Fsn0503h)Anti-CTSS/Cathepsin S Reference Antibody (Fsn0503h) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02514-1-sec-hplc.jpgAnti-CTSS / Cathepsin S Reference Antibody (Fsn0503h)The purity of Anti-CTSS/Cathepsin S Reference Antibody (Fsn0503h)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287332026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02539-2-sds-page.jpgAnti-LOXL2 Reference Antibody (simtuzumab)Anti-LOXL2 Reference Antibody (simtuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02539-2-sec-hplc.jpgAnti-LOXL2 Reference Antibody (simtuzumab)The purity of Anti-LOXL2 Reference Antibody (simtuzumab)is more than 99.41%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02539-2-od450.jpgAnti-LOXL2 Reference Antibody (simtuzumab)Immobilized human LOXL2 His at 2 &mug/mL can bind Anti-LOXL2 Reference Antibody (simtuzumab) https://www.bosterbio.com/catalog/product/view/id/1287342026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-11-sds-page.jpgAnti-TNFSF4 / OX40L / CD252 Reference Antibody (oxelumab)Anti-TNFSF4/OX40L/CD252 Reference Antibody (oxelumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-11-sec-hplc.jpgAnti-TNFSF4 / OX40L / CD252 Reference Antibody (oxelumab)The purity of Anti-TNFSF4/OX40L/CD252 Reference Antibody (oxelumab)is more than 99.04% https://www.bosterbio.com/catalog/product/view/id/1287352026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-12-sds-page.jpgAnti-TNFSF4 / OX40L / CD252 Reference Antibody (amlitelimab)Anti-TNFSF4/OX40L/CD252 Reference Antibody (amlitelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02495-12-sec-hplc.jpgAnti-TNFSF4 / OX40L / CD252 Reference Antibody (amlitelimab)The purity of Anti-TNFSF4/OX40L/CD252 Reference Antibody (amlitelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287362026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02614-sds-page.jpgAnti-Matriptase Reference Antibody (Oxford Bio patent anti-Matriptase)Anti-Matriptase Reference Antibody (Oxford Bio patent anti-Matriptase) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02614-sec-hplc.jpgAnti-Matriptase Reference Antibody (Oxford Bio patent anti-Matriptase)The purity of Anti-Matriptase Reference Antibody (Oxford Bio patent anti-Matriptase)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287372026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02657-sds-page.jpgAnti-PSCA Reference Antibody (AGS-1C4D4)Anti-PSCA Reference Antibody (AGS-1C4D4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 97.9%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02657-sec-hplc.jpgAnti-PSCA Reference Antibody (AGS-1C4D4)The purity of Anti-PSCA Reference Antibody (AGS-1C4D4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287382026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-7-sds-page.jpgAnti-CD3e Reference Antibody (foralumab)Anti-CD3e Reference Antibody (foralumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-7-sec-hplc.jpgAnti-CD3e Reference Antibody (foralumab)The purity of Anti-CD3e Reference Antibody (foralumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287392026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-8-sds-page.jpgAnti-CD3 Reference Antibody (visilizumab)Anti-CD3 Reference Antibody (visilizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-8-sec-hplc.jpgAnti-CD3 Reference Antibody (visilizumab)The purity of Anti-CD3 Reference Antibody (visilizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287402026-03-10T04:39:26+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1287412026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-6-sds-page.jpgAnti-CD3 Reference Antibody (otelixizumab)Anti-CD3 Reference Antibody (otelixizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02675-6-sec-hplc.jpgAnti-CD3 Reference Antibody (otelixizumab)The purity of Anti-CD3 Reference Antibody (otelixizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287422026-03-10T04:39:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02679-sds-page.jpgAnti-Fucosyl GM1 Reference Antibody (BMS-986012)Anti-Fucosyl GM1 Reference Antibody (BMS-986012) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02679-sec-hplc.jpgAnti-Fucosyl GM1 Reference Antibody (BMS-986012)The purity of Anti-Fucosyl GM1 Reference Antibody (BMS-986012)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287432026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02724-sds-page.jpgAnti-KIR2DL1 / CD158a Reference Antibody (Innate patent anti-KIR2DL)Anti-KIR2DL1/CD158a Reference Antibody (Innate patent anti-KIR2DL) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02724-sec-hplc.jpgAnti-KIR2DL1 / CD158a Reference Antibody (Innate patent anti-KIR2DL)The purity of Anti-KIR2DL1/CD158a Reference Antibody (Innate patent anti-KIR2DL)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287442026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02731-sds-page.jpgAnti-CLEC7A Reference Antibody (Baylor patent anti-Dectin-1)Anti-CLEC7A Reference Antibody (Baylor patent anti-Dectin-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02731-sec-hplc.jpgAnti-CLEC7A Reference Antibody (Baylor patent anti-Dectin-1)The purity of Anti-CLEC7A Reference Antibody (Baylor patent anti-Dectin-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287452026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02747-sds-page.jpgAnti-CXADR Reference Antibody (Med. Bio. Labs patent anti-CXADR)Anti-CXADR Reference Antibody (Med. Bio. Labs patent anti-CXADR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02747-sec-hplc.jpgAnti-CXADR Reference Antibody (Med. Bio. Labs patent anti-CXADR)The purity of Anti-CXADR Reference Antibody (Med. Bio. Labs patent anti-CXADR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287462026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02821-1-sds-page.jpgAnti-B7-H4 / VTCN1 Reference Antibody (alsevalimab)Anti-B7-H4/VTCN1 Reference Antibody (alsevalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02821-1-sec-hplc.jpgAnti-B7-H4 / VTCN1 Reference Antibody (alsevalimab)The purity of Anti-B7-H4/VTCN1 Reference Antibody (alsevalimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02821-1-od450.jpgAnti-B7-H4 / VTCN1 Reference Antibody (alsevalimab)Immobilized human B7 H4 His at 2 &mug/mL can bind Anti-B7-H4/VTCN1 Reference Antibody (alsevalimab) https://www.bosterbio.com/catalog/product/view/id/1287472026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02821-2-sds-page.jpgAnti-B7-H4 / VTCN1 Reference Antibody (Millennium patent anti-B7-H4)Anti-B7-H4/VTCN1 Reference Antibody (Millennium patent anti-B7-H4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02821-2-sec-hplc.jpgAnti-B7-H4 / VTCN1 Reference Antibody (Millennium patent anti-B7-H4)The purity of Anti-B7-H4/VTCN1 Reference Antibody (Millennium patent anti-B7-H4)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02821-2-od450.jpgAnti-B7-H4 / VTCN1 Reference Antibody (Millennium patent anti-B7-H4)Immobilized human B7 H4 at 2 &mug/mL can bind Anti-B7-H4/VTCN1 Reference Antibody (Millennium patent anti-B7-H4) https://www.bosterbio.com/catalog/product/view/id/1287482026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02824-sds-page.jpgAnti-IL-1RAP / IL-1R3 Reference Antibody (nidanilimab)Anti-IL-1RAP/IL-1R3 Reference Antibody (nidanilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02824-sec-hplc.jpgAnti-IL-1RAP / IL-1R3 Reference Antibody (nidanilimab)The purity of Anti-IL-1RAP/IL-1R3 Reference Antibody (nidanilimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287492026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02824-1-sds-page.jpgAnti-IL-1RAP / IL-1R3 Reference Antibody (Nadunolimab)Anti-IL-1RAP/IL-1R3 Reference Antibody (Nadunolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02824-1-sec-hplc.jpgAnti-IL-1RAP / IL-1R3 Reference Antibody (Nadunolimab)The purity of Anti-IL-1RAP/IL-1R3 Reference Antibody (Nadunolimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287502026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-5-sds-page.jpgAnti-FOLH1 / PSMA Reference Antibody (rosopatamab)Anti-FOLH1/PSMA Reference Antibody (rosopatamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-5-sec-hplc.jpgAnti-FOLH1 / PSMA Reference Antibody (rosopatamab)The purity of Anti-FOLH1/PSMA Reference Antibody (rosopatamab)is more than 97.15%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-5-od450.jpgAnti-FOLH1 / PSMA Reference Antibody (rosopatamab)Immobilized human FOLH1/PSMA https://www.bosterbio.com/catalog/product/view/id/1287512026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-6-sds-page.jpgAnti-FOLH1 / PSMA Reference Antibody (pelgifatamAb)Anti-FOLH1/PSMA Reference Antibody (pelgifatamAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-6-sec-hplc.jpgAnti-FOLH1 / PSMA Reference Antibody (pelgifatamAb)The purity of Anti-FOLH1/PSMA Reference Antibody (pelgifatamAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287522026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-7-sds-page.jpgAnti-FOLH1 / PSMA Reference Antibody (rosopatamab tetraxetan)Anti-FOLH1/PSMA Reference Antibody (rosopatamab tetraxetan) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-7-sec-hplc.jpgAnti-FOLH1 / PSMA Reference Antibody (rosopatamab tetraxetan)The purity of Anti-FOLH1/PSMA Reference Antibody (rosopatamab tetraxetan)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287532026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-8-sds-page.jpgAnti-FOLH1 / PSMA Reference Antibody (rosopatamab-MMAE)Anti-FOLH1/PSMA Reference Antibody (rosopatamab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02846-8-sec-hplc.jpgAnti-FOLH1 / PSMA Reference Antibody (rosopatamab-MMAE)The purity of Anti-FOLH1/PSMA Reference Antibody (rosopatamab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287542026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02851-sds-page.jpgAnti-AOC3 / VAP1 Reference Antibody (timolumab)Anti-AOC3/VAP1 Reference Antibody (timolumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02851-sec-hplc.jpgAnti-AOC3 / VAP1 Reference Antibody (timolumab)The purity of Anti-AOC3/VAP1 Reference Antibody (timolumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287552026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-1-sds-page.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (cusatuzumab)Anti-TNFSF7/CD27L/CD70 Reference Antibody (cusatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-1-sec-hplc.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (cusatuzumab)The purity of Anti-TNFSF7/CD27L/CD70 Reference Antibody (cusatuzumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-1-od450.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (cusatuzumab)Immobilized huaman CD70 FC at4 &mug/mL can bind Anti-TNFSF7/CD27L/CD70 Reference Antibody (cusatuzumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-1-facs.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (cusatuzumab)HL-60 cells were stained with Anti-TNFSF7/CD27L/CD70 Reference Antibody (cusatuzumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1287562026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-2-sds-page.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (Vorsetuzumab mafodotin)Anti-TNFSF7/CD27L/CD70 Reference Antibody (Vorsetuzumab mafodotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-2-sec-hplc.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (Vorsetuzumab mafodotin)The purity of Anti-TNFSF7/CD27L/CD70 Reference Antibody (Vorsetuzumab mafodotin)is more than 99.29% https://www.bosterbio.com/catalog/product/view/id/1287572026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-3-sds-page.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (vorsetuzumab)Anti-TNFSF7/CD27L/CD70 Reference Antibody (vorsetuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-3-sec-hplc.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (vorsetuzumab)The purity of Anti-TNFSF7/CD27L/CD70 Reference Antibody (vorsetuzumab)is more than 99.29%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-3-facs.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (vorsetuzumab)HL-60 cells were stained with Anti-TNFSF7/CD27L/CD70 Reference Antibody (vorsetuzumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02853-3-internalization-rate.jpgAnti-TNFSF7 / CD27L / CD70 Reference Antibody (vorsetuzumab)The endocytosis ratio vorsetuzumab by 786-O increased with the increase of antibody concentration https://www.bosterbio.com/catalog/product/view/id/1287582026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02857-1-sds-page.jpgAnti-RSPO1 Reference Antibody (Oncomed patent anti-RSPO1)Anti-RSPO1 Reference Antibody (Oncomed patent anti-RSPO1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02857-1-sec-hplc.jpgAnti-RSPO1 Reference Antibody (Oncomed patent anti-RSPO1)The purity of Anti-RSPO1 Reference Antibody (Oncomed patent anti-RSPO1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287592026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02865-1-sds-page.jpgAnti-TNFRSF13C / BAFFR / CD268 Reference Antibody (ianalumab)Anti-TNFRSF13C/BAFFR/CD268 Reference Antibody (ianalumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02865-1-sec-hplc.jpgAnti-TNFRSF13C / BAFFR / CD268 Reference Antibody (ianalumab)The purity of Anti-TNFRSF13C/BAFFR/CD268 Reference Antibody (ianalumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02865-1-od450.jpgAnti-TNFRSF13C / BAFFR / CD268 Reference Antibody (ianalumab)Immobilized human GPA33/A33 https://www.bosterbio.com/catalog/product/view/id/1287602026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-4-sds-page.jpgAnti-LAG3 / CD223 Reference Antibody (relatlimab)Anti-LAG3/CD223 Reference Antibody (relatlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-4-sec-hplc.jpgAnti-LAG3 / CD223 Reference Antibody (relatlimab)The purity of Anti-LAG3/CD223 Reference Antibody (relatlimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-4-od450.jpgAnti-LAG3 / CD223 Reference Antibody (relatlimab)Immobilized human LAG3 His at 2 &mug/mL can bind Anti-LAG3/CD223 Reference Antibody (relatlimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-4-facs.jpgAnti-LAG3 / CD223 Reference Antibody (relatlimab)Human LAG3 CHO cells were stained with Anti-LAG3/CD223 Reference Antibody (relatlimab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-4-syngeneic-mc38-model.jpgAnti-LAG3 / CD223 Reference Antibody (relatlimab)Relatlimab inhibited the tumor growth of MC38 on Human LAG3 mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1287612026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-5-sds-page.jpgAnti-LAG3 / CD223 Reference Antibody (fianlimab)Anti-LAG3/CD223 Reference Antibody (fianlimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-5-sec-hplc.jpgAnti-LAG3 / CD223 Reference Antibody (fianlimab)The purity of Anti-LAG3/CD223 Reference Antibody (fianlimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287622026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-6-sds-page.jpgAnti-LAG3 / CD223 Reference Antibody (favezelimab)Anti-LAG3/CD223 Reference Antibody (favezelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-6-sec-hplc.jpgAnti-LAG3 / CD223 Reference Antibody (favezelimab)The purity of Anti-LAG3/CD223 Reference Antibody (favezelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287632026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-7-sds-page.jpgAnti-LAG3 / CD223 Reference Antibody (ieramilimab)Anti-LAG3/CD223 Reference Antibody (ieramilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-7-sec-hplc.jpgAnti-LAG3 / CD223 Reference Antibody (ieramilimab)The purity of Anti-LAG3/CD223 Reference Antibody (ieramilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287642026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-8-sds-page.jpgAnti-LAG3 / CD223 Reference Antibody (encelimab)Anti-LAG3/CD223 Reference Antibody (encelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-8-sec-hplc.jpgAnti-LAG3 / CD223 Reference Antibody (encelimab)The purity of Anti-LAG3/CD223 Reference Antibody (encelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287652026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-9-sds-page.jpgAnti-LAG3 / CD223 Reference Antibody (miptenalimab)Anti-LAG3/CD223 Reference Antibody (miptenalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02869-9-sec-hplc.jpgAnti-LAG3 / CD223 Reference Antibody (miptenalimab)The purity of Anti-LAG3/CD223 Reference Antibody (miptenalimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287662026-03-10T04:39:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02872-sds-page.jpgAnti-EphA3 Reference Antibody (ifabotuzumab)Anti-EphA3 Reference Antibody (ifabotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02872-sec-hplc.jpgAnti-EphA3 Reference Antibody (ifabotuzumab)The purity of Anti-EphA3 Reference Antibody (ifabotuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287672026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02925-2-sds-page.jpgAnti-IL-9 Reference Antibody (enokizumab)Anti-IL-9 Reference Antibody (enokizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02925-2-sec-hplc.jpgAnti-IL-9 Reference Antibody (enokizumab)The purity of Anti-IL-9 Reference Antibody (enokizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287682026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02929-2-sds-page.jpgAnti-ANGPTL3 Reference Antibody (evinacumab)Anti-ANGPTL3 Reference Antibody (evinacumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02929-2-sec-hplc.jpgAnti-ANGPTL3 Reference Antibody (evinacumab)The purity of Anti-ANGPTL3 Reference Antibody (evinacumab)is more than 99.48% https://www.bosterbio.com/catalog/product/view/id/1287692026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02957-1-sds-page.jpgAnti-PTK7 / CCK4 Reference Antibody (cofetuzumab)Anti-PTK7/CCK4 Reference Antibody (cofetuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02957-1-sec-hplc.jpgAnti-PTK7 / CCK4 Reference Antibody (cofetuzumab)The purity of Anti-PTK7/CCK4 Reference Antibody (cofetuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287702026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02959-1-sds-page.jpgAnti-IL-2Rb / CD122 Reference Antibody (Singapore ASTR patent anti-IL-2R beta / IL-2R gamma )Anti-IL-2Rb/CD122 Reference Antibody (Singapore ASTR patent anti-IL-2R beta/IL-2R gamma ) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02959-1-sec-hplc.jpgAnti-IL-2Rb / CD122 Reference Antibody (Singapore ASTR patent anti-IL-2R beta / IL-2R gamma )The purity of Anti-IL-2Rb/CD122 Reference Antibody (Singapore ASTR patent anti-IL-2R beta/IL-2R gamma )is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287712026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02975-4-sds-page.jpgAnti-GOLM1 Reference Antibody (Cureab patent anti-GP73)Anti-GOLM1 Reference Antibody (Cureab patent anti-GP73) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02975-4-sec-hplc.jpgAnti-GOLM1 Reference Antibody (Cureab patent anti-GP73)The purity of Anti-GOLM1 Reference Antibody (Cureab patent anti-GP73)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287722026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02979-1-sds-page.jpgAnti-ABCB5 Reference Antibody (Brigham and Women's patent anti-ABCB5)Anti-ABCB5 Reference Antibody (Brigham and Women's patent anti-ABCB5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02979-1-sec-hplc.jpgAnti-ABCB5 Reference Antibody (Brigham and Women's patent anti-ABCB5)The purity of Anti-ABCB5 Reference Antibody (Brigham and Women's patent anti-ABCB5)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287732026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02997-6-sds-page.jpgAnti-Endoglin / CD105 Reference Antibody (carotuximab-MMAE)Anti-Endoglin/CD105 Reference Antibody (carotuximab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02997-6-sec-hplc.jpgAnti-Endoglin / CD105 Reference Antibody (carotuximab-MMAE)The purity of Anti-Endoglin/CD105 Reference Antibody (carotuximab-MMAE)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02997-6-od450.jpgAnti-Endoglin / CD105 Reference Antibody (carotuximab-MMAE)Immobilized human CD105 His at 2 &mug/mL can bind Anti-Endoglin/CD105 Reference Antibody (carotuximab-MMAE) https://www.bosterbio.com/catalog/product/view/id/1287742026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02997-7-sds-page.jpgAnti-Endoglin / CD105 Reference Antibody (carotuximab)Anti-Endoglin/CD105 Reference Antibody (carotuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m02997-7-sec-hplc.jpgAnti-Endoglin / CD105 Reference Antibody (carotuximab)The purity of Anti-Endoglin/CD105 Reference Antibody (carotuximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287752026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03019-2-sds-page.jpgAnti-Siglec-4a / MAG Reference Antibody (refanezumab)Anti-Siglec-4a/MAG Reference Antibody (refanezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03019-2-sec-hplc.jpgAnti-Siglec-4a / MAG Reference Antibody (refanezumab)The purity of Anti-Siglec-4a/MAG Reference Antibody (refanezumab)is more than 99.41%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03019-2-od450.jpgAnti-Siglec-4a / MAG Reference Antibody (refanezumab)Immobilized human Siglec 4a/MAG https://www.bosterbio.com/catalog/product/view/id/1287762026-03-16T05:08:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03036-1-sds-page.jpgAnti-SLC7A11 Reference Antibody (Agilvax Patent Anti-Slc7A11)Anti-SLC7A11 Reference Antibody (Agilvax Patent Anti-Slc7A11) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03036-1-sec-hplc.jpgAnti-SLC7A11 Reference Antibody (Agilvax Patent Anti-Slc7A11)The purity of Anti-SLC7A11 Reference Antibody (Agilvax Patent Anti-Slc7A11)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287772026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03074-sds-page.jpgAnti-ADAM9 Reference Antibody (Imgc936)Anti-ADAM9 Reference Antibody (Imgc936) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03074-sec-hplc.jpgAnti-ADAM9 Reference Antibody (Imgc936)The purity of Anti-ADAM9 Reference Antibody (Imgc936)is more than 98.27%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03074-facs.jpgAnti-ADAM9 Reference Antibody (Imgc936)Human ADAM9 CHOS cells were stained with Anti-ADAM9 Reference Antibody (Imgc936) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03074-inhibition-of-cell-growth.jpgAnti-ADAM9 Reference Antibody (Imgc936)The endocytosis ratio Imgc936 by Human ADAM9 HT29 increased with the increase of antibody concentration https://www.bosterbio.com/catalog/product/view/id/1287782026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03092-sds-page.jpgAnti-PDGFC / VEGFE Reference Antibody (Thrombogenics patent anti-PDGF-C)Anti-PDGFC/VEGFE Reference Antibody (Thrombogenics patent anti-PDGF-C) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03092-sec-hplc.jpgAnti-PDGFC / VEGFE Reference Antibody (Thrombogenics patent anti-PDGF-C)The purity of Anti-PDGFC/VEGFE Reference Antibody (Thrombogenics patent anti-PDGF-C)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287792026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03093-2-sds-page.jpgAnti-DSG3 Reference Antibody (Forerunner patent anti-DSG3)Anti-DSG3 Reference Antibody (Forerunner patent anti-DSG3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03093-2-sec-hplc.jpgAnti-DSG3 Reference Antibody (Forerunner patent anti-DSG3)The purity of Anti-DSG3 Reference Antibody (Forerunner patent anti-DSG3)is more than 99.63% https://www.bosterbio.com/catalog/product/view/id/1287802026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03125-4-sds-page.jpgAnti-TNFRSF18 / GITR / CD357 Reference Antibody (ragifilimab)Anti-TNFRSF18/GITR/CD357 Reference Antibody (ragifilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03125-4-sec-hplc.jpgAnti-TNFRSF18 / GITR / CD357 Reference Antibody (ragifilimab)The purity of Anti-TNFRSF18/GITR/CD357 Reference Antibody (ragifilimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287812026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03125-5-sds-page.jpgAnti-TNFRSF18 / GITR / CD357 Reference Antibody (Korea Natl.Cancer Ctr. patent anti-GITR)Anti-TNFRSF18/GITR/CD357 Reference Antibody (Korea Natl.Cancer Ctr. patent anti-GITR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03125-5-sec-hplc.jpgAnti-TNFRSF18 / GITR / CD357 Reference Antibody (Korea Natl.Cancer Ctr. patent anti-GITR)The purity of Anti-TNFRSF18/GITR/CD357 Reference Antibody (Korea Natl.Cancer Ctr. patent anti-GITR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287822026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03142-2-sds-page.jpgAnti-GAD65 Reference Antibody (U.Washington patent anti-GAD65)Anti-GAD65 Reference Antibody (U.Washington patent anti-GAD65) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03142-2-sec-hplc.jpgAnti-GAD65 Reference Antibody (U.Washington patent anti-GAD65)The purity of Anti-GAD65 Reference Antibody (U.Washington patent anti-GAD65)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1287832026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03149-3-sds-page.jpgAnti-BTLA / CD272 Reference Antibody (icatolimab)Anti-BTLA/CD272 Reference Antibody (icatolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03149-3-sec-hplc.jpgAnti-BTLA / CD272 Reference Antibody (icatolimab)The purity of Anti-BTLA/CD272 Reference Antibody (icatolimab)is more than 96.73%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03149-3-od450.jpgAnti-BTLA / CD272 Reference Antibody (icatolimab)Immobilized human BTLA His at 2 &mug/mL can bind Anti-BTLA/CD272 Reference Antibody (icatolimab) https://www.bosterbio.com/catalog/product/view/id/1287842026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03149-4-sds-page.jpgAnti-BTLA / CD272 Reference Antibody (Tifcemalimab)Anti-BTLA/CD272 Reference Antibody (Tifcemalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03149-4-sec-hplc.jpgAnti-BTLA / CD272 Reference Antibody (Tifcemalimab)The purity of Anti-BTLA/CD272 Reference Antibody (Tifcemalimab)is more than 98.17% https://www.bosterbio.com/catalog/product/view/id/1287852026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03192-1-sds-page.jpgAnti-ROR1 Reference Antibody (zilovertamab)Anti-ROR1 Reference Antibody (zilovertamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03192-1-sec-hplc.jpgAnti-ROR1 Reference Antibody (zilovertamab)The purity of Anti-ROR1 Reference Antibody (zilovertamab)is more than 98.21%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03192-1-od450.jpgAnti-ROR1 Reference Antibody (zilovertamab)Immobilized human ROR1 His at 2 &mug/mL can bind Anti-ROR1 Reference Antibody (zilovertamab) https://www.bosterbio.com/catalog/product/view/id/1287862026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03192-2-sds-page.jpgAnti-ROR1 Reference Antibody (zilovertamab vedotin)Anti-ROR1 Reference Antibody (zilovertamab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03192-2-sec-hplc.jpgAnti-ROR1 Reference Antibody (zilovertamab vedotin)The purity of Anti-ROR1 Reference Antibody (zilovertamab vedotin)is more than 98.21%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03192-2-od450.jpgAnti-ROR1 Reference Antibody (zilovertamab vedotin)Immobilized human ROR1 His at 2 &mug/mL can bind Anti-ROR1 Reference Antibody (zilovertamab vedotin)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03192-2-xenograft-mda-mb-231-cell-model.jpgAnti-ROR1 Reference Antibody (zilovertamab vedotin)zilovertamab vedotin inhibited the tumor growth of MDA-MB-231on NSG mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1287872026-03-10T04:39:28+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03196-4-sds-page.jpgAnti-ENTPD1 / CD39 Reference Antibody (TTX-030)Anti-ENTPD1/CD39 Reference Antibody (TTX-030) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03196-4-sec-hplc.jpgAnti-ENTPD1 / CD39 Reference Antibody (TTX-030)The purity of Anti-ENTPD1/CD39 Reference Antibody (TTX-030)is more than 99.83%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03196-4-xenograft-molp-8-pbmc-cell-model.jpgAnti-ENTPD1 / CD39 Reference Antibody (TTX-030)TTX-030 inhibited the tumor growth of MOLP-8 on NCG mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1287882026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03197-2-sds-page.jpgAnti-CEACAM6 / CD66c Reference Antibody (tinurilimab)Anti-CEACAM6/CD66c Reference Antibody (tinurilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03197-2-sec-hplc.jpgAnti-CEACAM6 / CD66c Reference Antibody (tinurilimab)The purity of Anti-CEACAM6/CD66c Reference Antibody (tinurilimab)is more than 95.93%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03197-2-od450.jpgAnti-CEACAM6 / CD66c Reference Antibody (tinurilimab)Immobilized human CEACAM6 His at 2 &mug/mL can bind Anti-CEACAM6/CD66c Reference Antibody (tinurilimab) https://www.bosterbio.com/catalog/product/view/id/1287892026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03197-3-sds-page.jpgAnti-CEACAM6 / CD66c Reference Antibody (NEO-201)Anti-CEACAM6/CD66c Reference Antibody (NEO-201) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03197-3-sec-hplc.jpgAnti-CEACAM6 / CD66c Reference Antibody (NEO-201)The purity of Anti-CEACAM6/CD66c Reference Antibody (NEO-201)is more than 99.21% https://www.bosterbio.com/catalog/product/view/id/1287902026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03212-1-sds-page.jpgAnti-MAGEA3 Reference Antibody (CT Atlantic patent anti-MAGE-A3)Anti-MAGEA3 Reference Antibody (CT Atlantic patent anti-MAGE-A3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03212-1-sec-hplc.jpgAnti-MAGEA3 Reference Antibody (CT Atlantic patent anti-MAGE-A3)The purity of Anti-MAGEA3 Reference Antibody (CT Atlantic patent anti-MAGE-A3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287912026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-3-sds-page.jpgAnti-Mesothelin Reference Antibody (anetumab-MMAE)Anti-Mesothelin Reference Antibody (anetumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-3-sec-hplc.jpgAnti-Mesothelin Reference Antibody (anetumab-MMAE)The purity of Anti-Mesothelin Reference Antibody (anetumab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287922026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-4-sds-page.jpgAnti-Mesothelin Reference Antibody (amatuximab)Anti-Mesothelin Reference Antibody (amatuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-4-sec-hplc.jpgAnti-Mesothelin Reference Antibody (amatuximab)The purity of Anti-Mesothelin Reference Antibody (amatuximab)is more than 99.47%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-4-od450.jpgAnti-Mesothelin Reference Antibody (amatuximab)Immobilized human Mesothelin His at 2 &mug/mL can bind Anti-Mesothelin Reference Antibody (amatuximab) https://www.bosterbio.com/catalog/product/view/id/1287932026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-5-sds-page.jpgAnti-Mesothelin Reference Antibody (anetumab)Anti-Mesothelin Reference Antibody (anetumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-5-sec-hplc.jpgAnti-Mesothelin Reference Antibody (anetumab)The purity of Anti-Mesothelin Reference Antibody (anetumab)is more than 98.58%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-5-od450.jpgAnti-Mesothelin Reference Antibody (anetumab)Immobilized human Mesothelin His at 2 &mug/mL can bind Anti-Mesothelin Reference Antibody (anetumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-5-facs.jpgAnti-Mesothelin Reference Antibody (anetumab)ASPC-1 cells were stained with Anti-Mesothelin Reference Antibody (anetumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1287942026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-6-sds-page.jpgAnti-Mesothelin Reference Antibody (BMS-986148)Anti-Mesothelin Reference Antibody (BMS-986148) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-6-sec-hplc.jpgAnti-Mesothelin Reference Antibody (BMS-986148)The purity of Anti-Mesothelin Reference Antibody (BMS-986148)is more than 96.7% https://www.bosterbio.com/catalog/product/view/id/1287952026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-7-sds-page.jpgAnti-Mesothelin Reference Antibody (anetumab ravtansine)Anti-Mesothelin Reference Antibody (anetumab ravtansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-7-sec-hplc.jpgAnti-Mesothelin Reference Antibody (anetumab ravtansine)The purity of Anti-Mesothelin Reference Antibody (anetumab ravtansine)is more than 98.58% https://www.bosterbio.com/catalog/product/view/id/1287962026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-8-sds-page.jpgAnti-Mesothelin Reference Antibody (NIH patent anti-Mesothelin)Anti-Mesothelin Reference Antibody (NIH patent anti-Mesothelin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03266-8-sec-hplc.jpgAnti-Mesothelin Reference Antibody (NIH patent anti-Mesothelin)The purity of Anti-Mesothelin Reference Antibody (NIH patent anti-Mesothelin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287972026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03281-2-sds-page.jpgAnti-CD48 Reference Antibody (Regeneron patent anti-CD48)Anti-CD48 Reference Antibody (Regeneron patent anti-CD48) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03281-2-sec-hplc.jpgAnti-CD48 Reference Antibody (Regeneron patent anti-CD48)The purity of Anti-CD48 Reference Antibody (Regeneron patent anti-CD48)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1287982026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03342-sds-page.jpgAnti-GCGR Reference Antibody (crotedumab)Anti-GCGR Reference Antibody (crotedumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03342-sec-hplc.jpgAnti-GCGR Reference Antibody (crotedumab)The purity of Anti-GCGR Reference Antibody (crotedumab)is more than 96.61%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03342-facs.jpgAnti-GCGR Reference Antibody (crotedumab)Human GCCR His EGFP HEK293 cells were stained with Anti-GCGR Reference Antibody (crotedumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1287992026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03342-1-sds-page.jpgAnti-GCGR Reference Antibody (volagidemab)Anti-GCGR Reference Antibody (volagidemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03342-1-sec-hplc.jpgAnti-GCGR Reference Antibody (volagidemab)The purity of Anti-GCGR Reference Antibody (volagidemab)is more than 98.43% https://www.bosterbio.com/catalog/product/view/id/1288002026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03353-2-sds-page.jpgAnti-CDH3 / P-cadherin Reference Antibody (PF-03732010)Anti-CDH3/P-cadherin Reference Antibody (PF-03732010) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03353-2-sec-hplc.jpgAnti-CDH3 / P-cadherin Reference Antibody (PF-03732010)The purity of Anti-CDH3/P-cadherin Reference Antibody (PF-03732010)is more than 99.39%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03353-2-facs.jpgAnti-CDH3 / P-cadherin Reference Antibody (PF-03732010)Human CDH3 HEK293 cells were stained with Anti-CDH3/P-cadherin Reference Antibody (PF-03732010) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1288012026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03438-3-sds-page.jpgAnti-AGER / RAGE Reference Antibody (XT-M4)Anti-AGER/RAGE Reference Antibody (XT-M4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03438-3-sec-hplc.jpgAnti-AGER / RAGE Reference Antibody (XT-M4)The purity of Anti-AGER/RAGE Reference Antibody (XT-M4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288022026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03484-3-sds-page.jpgAnti-CD52 Reference Antibody (gatralimab)Anti-CD52 Reference Antibody (gatralimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03484-3-sec-hplc.jpgAnti-CD52 Reference Antibody (gatralimab)The purity of Anti-CD52 Reference Antibody (gatralimab)is more than 97.94% https://www.bosterbio.com/catalog/product/view/id/1288032026-03-17T05:16:07+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03507-1-sds-page.jpgAnti-KLK5 / Kallikrein 5 Reference Antibody (Genentech patent anti-KLK5)Anti-KLK5/Kallikrein 5 Reference Antibody (Genentech patent anti-KLK5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03507-1-sec-hplc.jpgAnti-KLK5 / Kallikrein 5 Reference Antibody (Genentech patent anti-KLK5)The purity of Anti-KLK5/Kallikrein 5 Reference Antibody (Genentech patent anti-KLK5)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288042026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03551-sds-page.jpgAnti-SOST / Sclerostin Reference Antibody (blosozumab)Anti-SOST/Sclerostin Reference Antibody (blosozumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03551-sec-hplc.jpgAnti-SOST / Sclerostin Reference Antibody (blosozumab)The purity of Anti-SOST/Sclerostin Reference Antibody (blosozumab)is more than 98.7% https://www.bosterbio.com/catalog/product/view/id/1288052026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03551-1-sds-page.jpgAnti-SOST / Sclerostin Reference Antibody (setrusumab)Anti-SOST/Sclerostin Reference Antibody (setrusumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03551-1-sec-hplc.jpgAnti-SOST / Sclerostin Reference Antibody (setrusumab)The purity of Anti-SOST/Sclerostin Reference Antibody (setrusumab)is more than 91.76% https://www.bosterbio.com/catalog/product/view/id/1288062026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03551-2-sds-page.jpgAnti-SOST / Sclerostin Reference Antibody (romosozumab)Anti-SOST/Sclerostin Reference Antibody (romosozumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03551-2-sec-hplc.jpgAnti-SOST / Sclerostin Reference Antibody (romosozumab)The purity of Anti-SOST/Sclerostin Reference Antibody (romosozumab)is more than 99.11% https://www.bosterbio.com/catalog/product/view/id/1288072026-03-10T04:39:29+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-sds-page.jpgAnti-TROP2 Reference Antibody (sacituzumab)Anti-TROP2 Reference Antibody (sacituzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-sec-hplc.jpgAnti-TROP2 Reference Antibody (sacituzumab)The purity of Anti-TROP2 Reference Antibody (sacituzumab)is more than 96.23%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-od450.jpgAnti-TROP2 Reference Antibody (sacituzumab)Immobilized human TROP2 His at 2 &mug/mL can bind Anti-TROP2 Reference Antibody (sacituzumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-facs.jpgAnti-TROP2 Reference Antibody (sacituzumab)Human TROP2 HEK293 cells were stained with Anti-TROP2 Reference Antibody (sacituzumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-internalization-rate.jpgAnti-TROP2 Reference Antibody (sacituzumab)The endocytosis ratio sacituzumab by human TROP2 HEK293 increased with the increase of antibody concentration https://www.bosterbio.com/catalog/product/view/id/1288082026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-1-sds-page.jpgAnti-TROP2 Reference Antibody (Datopotamab)Anti-TROP2 Reference Antibody (Datopotamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-1-sec-hplc.jpgAnti-TROP2 Reference Antibody (Datopotamab)The purity of Anti-TROP2 Reference Antibody (Datopotamab)is more than 98.09%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-1-od450.jpgAnti-TROP2 Reference Antibody (Datopotamab)Immobilized human TROP2(ECD) His at 2 &mug/mL can bind Anti-TROP2 Reference Antibody (Datopotamab) https://www.bosterbio.com/catalog/product/view/id/1288092026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-2-sds-page.jpgAnti-TROP2 Reference Antibody (Sacituzumab govitecan)Anti-TROP2 Reference Antibody (Sacituzumab govitecan) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-2-sec-hplc.jpgAnti-TROP2 Reference Antibody (Sacituzumab govitecan)The purity of Anti-TROP2 Reference Antibody (Sacituzumab govitecan)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288102026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-3-sds-page.jpgAnti-TROP2 Reference Antibody (datopotamab deruxtecan)Anti-TROP2 Reference Antibody (datopotamab deruxtecan) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-3-sec-hplc.jpgAnti-TROP2 Reference Antibody (datopotamab deruxtecan)The purity of Anti-TROP2 Reference Antibody (datopotamab deruxtecan)is more than 98.09% https://www.bosterbio.com/catalog/product/view/id/1288112026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-4-sds-page.jpgAnti-TROP2 Reference Antibody (Sacituzumab-MMAE)Anti-TROP2 Reference Antibody (Sacituzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-4-sec-hplc.jpgAnti-TROP2 Reference Antibody (Sacituzumab-MMAE)The purity of Anti-TROP2 Reference Antibody (Sacituzumab-MMAE)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03569-4-mda-mb-231-cell-model.jpgAnti-TROP2 Reference Antibody (Sacituzumab-MMAE)Sacituzumab-ADC inhibited the tumor growth of MDA-MB-231 on NSG mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1288122026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03651-5-sds-page.jpgAnti-ICAM3 / CD50 Reference Antibody (Forerunner patent anti-ICAM-3)Anti-ICAM3/CD50 Reference Antibody (Forerunner patent anti-ICAM-3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03651-5-sec-hplc.jpgAnti-ICAM3 / CD50 Reference Antibody (Forerunner patent anti-ICAM-3)The purity of Anti-ICAM3/CD50 Reference Antibody (Forerunner patent anti-ICAM-3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288132026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03674-2-sds-page.jpgAnti-P-Selectin / CD62p Reference Antibody (inclacumab)Anti-P-Selectin/CD62p Reference Antibody (inclacumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03674-2-sec-hplc.jpgAnti-P-Selectin / CD62p Reference Antibody (inclacumab)The purity of Anti-P-Selectin/CD62p Reference Antibody (inclacumab)is more than 99.89% https://www.bosterbio.com/catalog/product/view/id/1288142026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03674-3-sds-page.jpgAnti-PSGL1 / CD162 Reference Antibody (neihulizumab)Anti-PSGL1/CD162 Reference Antibody (neihulizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03674-3-sec-hplc.jpgAnti-PSGL1 / CD162 Reference Antibody (neihulizumab)The purity of Anti-PSGL1/CD162 Reference Antibody (neihulizumab)is more than 99.48% https://www.bosterbio.com/catalog/product/view/id/1288152026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03677-sds-page.jpgAnti-KIR3DL2 / CD158k Reference Antibody (lacutamab)Anti-KIR3DL2/CD158k Reference Antibody (lacutamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03677-sec-hplc.jpgAnti-KIR3DL2 / CD158k Reference Antibody (lacutamab)The purity of Anti-KIR3DL2/CD158k Reference Antibody (lacutamab)is more than 99% https://www.bosterbio.com/catalog/product/view/id/1288162026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03694-sds-page.jpgAnti-GIPR Reference Antibody (Amgen patent anti-GIPR)Anti-GIPR Reference Antibody (Amgen patent anti-GIPR) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03694-sec-hplc.jpgAnti-GIPR Reference Antibody (Amgen patent anti-GIPR)The purity of Anti-GIPR Reference Antibody (Amgen patent anti-GIPR)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288172026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03707-sds-page.jpgAnti-OX2R / CD200R1 Reference Antibody (Janssen patent anti-CD200R1)Anti-OX2R/CD200R1 Reference Antibody (Janssen patent anti-CD200R1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03707-sec-hplc.jpgAnti-OX2R / CD200R1 Reference Antibody (Janssen patent anti-CD200R1)The purity of Anti-OX2R/CD200R1 Reference Antibody (Janssen patent anti-CD200R1)is more than 99.29%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03707-od450.jpgAnti-OX2R / CD200R1 Reference Antibody (Janssen patent anti-CD200R1)Immobilized human CD200R His at 2 &mug/mL can bind Anti-OX2R/CD200R1 Reference Antibody (Janssen patent anti-CD200R1) https://www.bosterbio.com/catalog/product/view/id/1288182026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-7-sds-page.jpgAnti-CD20 Reference Antibody (obinutuzumab)Anti-CD20 Reference Antibody (obinutuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-7-sec-hplc.jpgAnti-CD20 Reference Antibody (obinutuzumab)The purity of Anti-CD20 Reference Antibody (obinutuzumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-7-od450.jpgAnti-CD20 Reference Antibody (obinutuzumab)Immobilized human CD20 His at 2 &mug/mL can bind Anti-CD20 Reference Antibody (obinutuzumab) https://www.bosterbio.com/catalog/product/view/id/1288192026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-19-sds-page.jpgAnti-CD20 Reference Antibody (TRU-015)Anti-CD20 Reference Antibody (TRU-015) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-19-sec-hplc.jpgAnti-CD20 Reference Antibody (TRU-015)The purity of Anti-CD20 Reference Antibody (TRU-015)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288202026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-9-sds-page.jpgAnti-CD20 Reference Antibody (ripertamab)Anti-CD20 Reference Antibody (ripertamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-9-sec-hplc.jpgAnti-CD20 Reference Antibody (ripertamab)The purity of Anti-CD20 Reference Antibody (ripertamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288212026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-10-sds-page.jpgAnti-CD20 Reference Antibody (ocrelizumab)Anti-CD20 Reference Antibody (ocrelizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-10-sec-hplc.jpgAnti-CD20 Reference Antibody (ocrelizumab)The purity of Anti-CD20 Reference Antibody (ocrelizumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-10-facs.jpgAnti-CD20 Reference Antibody (ocrelizumab)Human CD20 CHO-K1 cells were stained with Anti-CD20 Reference Antibody (ocrelizumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1288222026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-11-sds-page.jpgAnti-CD20 Reference Antibody (ublituximab)Anti-CD20 Reference Antibody (ublituximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-11-sec-hplc.jpgAnti-CD20 Reference Antibody (ublituximab)The purity of Anti-CD20 Reference Antibody (ublituximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288232026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-12-sds-page.jpgAnti-CD20 Reference Antibody (ofatumumab)Anti-CD20 Reference Antibody (ofatumumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-12-sec-hplc.jpgAnti-CD20 Reference Antibody (ofatumumab)The purity of Anti-CD20 Reference Antibody (ofatumumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-12-facs.jpgAnti-CD20 Reference Antibody (ofatumumab)Romas cells were stained with Anti-CD20 Reference Antibody (ofatumumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1288242026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-13-sds-page.jpgAnti-CD20 Reference Antibody (zuberitamab)Anti-CD20 Reference Antibody (zuberitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-13-sec-hplc.jpgAnti-CD20 Reference Antibody (zuberitamab)The purity of Anti-CD20 Reference Antibody (zuberitamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288252026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-14-sds-page.jpgAnti-CD20 Reference Antibody (veltuzumab)Anti-CD20 Reference Antibody (veltuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-14-sec-hplc.jpgAnti-CD20 Reference Antibody (veltuzumab)The purity of Anti-CD20 Reference Antibody (veltuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288262026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-15-sds-page.jpgAnti-CD20 Reference Antibody (ocaratuzumab)Anti-CD20 Reference Antibody (ocaratuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-15-sec-hplc.jpgAnti-CD20 Reference Antibody (ocaratuzumab)The purity of Anti-CD20 Reference Antibody (ocaratuzumab)is more than 99.58% https://www.bosterbio.com/catalog/product/view/id/1288272026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-16-sds-page.jpgAnti-CD20 Reference Antibody (divozilimab)Anti-CD20 Reference Antibody (divozilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-16-sec-hplc.jpgAnti-CD20 Reference Antibody (divozilimab)The purity of Anti-CD20 Reference Antibody (divozilimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288282026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-17-sds-page.jpgAnti-CD20 Reference Antibody (ibritumomab)Anti-CD20 Reference Antibody (ibritumomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-17-sec-hplc.jpgAnti-CD20 Reference Antibody (ibritumomab)The purity of Anti-CD20 Reference Antibody (ibritumomab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288292026-03-10T04:39:30+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-8-sds-page.jpgAnti-CD20 Reference Antibody (Regeneron patent anti-CD20)Anti-CD20 Reference Antibody (Regeneron patent anti-CD20) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03780-8-sec-hplc.jpgAnti-CD20 Reference Antibody (Regeneron patent anti-CD20)The purity of Anti-CD20 Reference Antibody (Regeneron patent anti-CD20)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288302026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03838-1-sds-page.jpgAnti-INHBB / Activin B Reference Antibody (Oxford Brookes U. patent anti-Activin Beta-B)Anti-INHBB/Activin B Reference Antibody (Oxford Brookes U. patent anti-Activin Beta-B) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03838-1-sec-hplc.jpgAnti-INHBB / Activin B Reference Antibody (Oxford Brookes U. patent anti-Activin Beta-B)The purity of Anti-INHBB/Activin B Reference Antibody (Oxford Brookes U. patent anti-Activin Beta-B)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288312026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03846-4-sds-page.jpgAnti-TMEFF2 Reference Antibody (Janssen patent anti-TMEFF2)Anti-TMEFF2 Reference Antibody (Janssen patent anti-TMEFF2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03846-4-sec-hplc.jpgAnti-TMEFF2 Reference Antibody (Janssen patent anti-TMEFF2)The purity of Anti-TMEFF2 Reference Antibody (Janssen patent anti-TMEFF2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288322026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03871-1-sds-page.jpgAnti-GPC1 / Glypican-1 Reference Antibody (Minomic patent anti-Glypican 1)Anti-GPC1/Glypican-1 Reference Antibody (Minomic patent anti-Glypican 1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03871-1-sec-hplc.jpgAnti-GPC1 / Glypican-1 Reference Antibody (Minomic patent anti-Glypican 1)The purity of Anti-GPC1/Glypican-1 Reference Antibody (Minomic patent anti-Glypican 1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288332026-03-25T05:24:59+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03879-2-sds-page.jpgAnti-KLK2 / Kallikrein 2 Reference Antibody (JNJ-69086420)Anti-KLK2/Kallikrein 2 Reference Antibody (JNJ-69086420) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03879-2-sec-hplc.jpgAnti-KLK2 / Kallikrein 2 Reference Antibody (JNJ-69086420)The purity of Anti-KLK2/Kallikrein 2 Reference Antibody (JNJ-69086420)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288342026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03913-3-sds-page.jpgAnti-CD6 Reference Antibody (itolizumab)Anti-CD6 Reference Antibody (itolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03913-3-sec-hplc.jpgAnti-CD6 Reference Antibody (itolizumab)The purity of Anti-CD6 Reference Antibody (itolizumab)is more than 100.00% https://www.bosterbio.com/catalog/product/view/id/1288352026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03957-sds-page.jpgAnti-NaPi2b / SLC34A2 Reference Antibody (upifitamab)Anti-NaPi2b/SLC34A2 Reference Antibody (upifitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03957-sec-hplc.jpgAnti-NaPi2b / SLC34A2 Reference Antibody (upifitamab)The purity of Anti-NaPi2b/SLC34A2 Reference Antibody (upifitamab)is more than 99.42%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03957-od450.jpgAnti-NaPi2b / SLC34A2 Reference Antibody (upifitamab)Immobilized human SLC34A2(188 361aa) Fc at 2 &mug/mL can bind Anti-NaPi2b/SLC34A2 Reference Antibody (upifitamab) https://www.bosterbio.com/catalog/product/view/id/1288362026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03957-1-sds-page.jpgAnti-NaPi2b / SLC34A2 Reference Antibody (lifastuzumab vedotin)Anti-NaPi2b/SLC34A2 Reference Antibody (lifastuzumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03957-1-sec-hplc.jpgAnti-NaPi2b / SLC34A2 Reference Antibody (lifastuzumab vedotin)The purity of Anti-NaPi2b/SLC34A2 Reference Antibody (lifastuzumab vedotin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288372026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03957-2-sds-page.jpgAnti-NaPi2b / SLC34A2 Reference Antibody (Lifastuzumab)Anti-NaPi2b/SLC34A2 Reference Antibody (Lifastuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03957-2-sec-hplc.jpgAnti-NaPi2b / SLC34A2 Reference Antibody (Lifastuzumab)The purity of Anti-NaPi2b/SLC34A2 Reference Antibody (Lifastuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288382026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03970-1-sds-page.jpgAnti-AMHR2 Reference Antibody (murlentamab)Anti-AMHR2 Reference Antibody (murlentamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 93%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03970-1-sec-hplc.jpgAnti-AMHR2 Reference Antibody (murlentamab)The purity of Anti-AMHR2 Reference Antibody (murlentamab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288392026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03970-2-sds-page.jpgAnti-AMHR2 Reference Antibody (murlentamab-MMAE)Anti-AMHR2 Reference Antibody (murlentamab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03970-2-sec-hplc.jpgAnti-AMHR2 Reference Antibody (murlentamab-MMAE)The purity of Anti-AMHR2 Reference Antibody (murlentamab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288402026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04011-2-sds-page.jpgAnti-EGFL7 Reference Antibody (parsatuzumab)Anti-EGFL7 Reference Antibody (parsatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04011-2-sec-hplc.jpgAnti-EGFL7 Reference Antibody (parsatuzumab)The purity of Anti-EGFL7 Reference Antibody (parsatuzumab)is more than 91.58% https://www.bosterbio.com/catalog/product/view/id/1288412026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04042-sds-page.jpgAnti-CALCRL / CGRPR Reference Antibody (erenumab)Anti-CALCRL/CGRPR Reference Antibody (erenumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04042-sec-hplc.jpgAnti-CALCRL / CGRPR Reference Antibody (erenumab)The purity of Anti-CALCRL/CGRPR Reference Antibody (erenumab)is more than 99.43%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04042-od450.jpgAnti-CALCRL / CGRPR Reference Antibody (erenumab)Immobilized human CGRPR VLP Protein at 16 &mug/mL can bind Anti-CALCRL/CGRPR Reference Antibody (erenumab) https://www.bosterbio.com/catalog/product/view/id/1288422026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04061-sds-page.jpgAnti-OSMR Reference Antibody (vixarelimab)Anti-OSMR Reference Antibody (vixarelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04061-sec-hplc.jpgAnti-OSMR Reference Antibody (vixarelimab)The purity of Anti-OSMR Reference Antibody (vixarelimab)is more than 96.9%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04061-od450.jpgAnti-OSMR Reference Antibody (vixarelimab)Immobilized human OSMR His at 2 &mug/mL can bind Anti-OSMR Reference Antibody (vixarelimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04061-facs.jpgAnti-OSMR Reference Antibody (vixarelimab)Human OSMR HEK293 cells were stained with Anti-OSMR Reference Antibody (vixarelimab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04061-od450-1.jpgAnti-OSMR Reference Antibody (vixarelimab)Anti-OSMR Reference Antibody (vixarelimab) P-STAT3 Assay was evaluated using NHDF. The IC50 was approximately 0.3493 nM.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04061-mcp-1.jpgAnti-OSMR Reference Antibody (vixarelimab)Anti-OSMR Reference Antibody (vixarelimab) MCP-1 secretion was evaluated using NHDF. The IC50 was approximately 0.0812 nM. https://www.bosterbio.com/catalog/product/view/id/1288432026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04070-2-sds-page.jpgAnti-MRC2 / CD280 Reference Antibody (Copenhagen Rigshospitalet patent anti-uPARAP)Anti-MRC2/CD280 Reference Antibody (Copenhagen Rigshospitalet patent anti-uPARAP) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04070-2-sec-hplc.jpgAnti-MRC2 / CD280 Reference Antibody (Copenhagen Rigshospitalet patent anti-uPARAP)The purity of Anti-MRC2/CD280 Reference Antibody (Copenhagen Rigshospitalet patent anti-uPARAP)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288442026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04070-3-sds-page.jpgAnti-MRC2 / CD280 Reference Antibody (Quark patent anti-ENDO 180)Anti-MRC2/CD280 Reference Antibody (Quark patent anti-ENDO 180) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04070-3-sec-hplc.jpgAnti-MRC2 / CD280 Reference Antibody (Quark patent anti-ENDO 180)The purity of Anti-MRC2/CD280 Reference Antibody (Quark patent anti-ENDO 180)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288452026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04070-4-sds-page.jpgAnti-MRC2 / CD280 Reference Antibody (Quark Patent Anti-Endo180)Anti-MRC2/CD280 Reference Antibody (Quark Patent Anti-Endo180) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04070-4-sec-hplc.jpgAnti-MRC2 / CD280 Reference Antibody (Quark Patent Anti-Endo180)The purity of Anti-MRC2/CD280 Reference Antibody (Quark Patent Anti-Endo180)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288462026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04083-1-sds-page.jpgAnti-SLAMF7 / CS1 Reference Antibody (azintuxizumAb)Anti-SLAMF7/CS1 Reference Antibody (azintuxizumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04083-1-sec-hplc.jpgAnti-SLAMF7 / CS1 Reference Antibody (azintuxizumAb)The purity of Anti-SLAMF7/CS1 Reference Antibody (azintuxizumAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288472026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04083-2-sds-page.jpgAnti-SLAMF7 / CS1 Reference Antibody (PDL241)Anti-SLAMF7/CS1 Reference Antibody (PDL241) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04083-2-sec-hplc.jpgAnti-SLAMF7 / CS1 Reference Antibody (PDL241)The purity of Anti-SLAMF7/CS1 Reference Antibody (PDL241)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288482026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04083-3-sds-page.jpgAnti-SLAMF7 / CS1 Reference Antibody (elotuzumab)Anti-SLAMF7/CS1 Reference Antibody (elotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04083-3-sec-hplc.jpgAnti-SLAMF7 / CS1 Reference Antibody (elotuzumab)The purity of Anti-SLAMF7/CS1 Reference Antibody (elotuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288492026-03-10T04:39:31+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04107-sds-page.jpgAnti-Alpha-synuclein Reference Antibody (prasinezumab)Anti-Alpha-synuclein Reference Antibody (prasinezumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04107-sec-hplc.jpgAnti-Alpha-synuclein Reference Antibody (prasinezumab)The purity of Anti-Alpha-synuclein Reference Antibody (prasinezumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288502026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04107-1-sds-page.jpgAnti-Alpha-synuclein Reference Antibody (cinpanemab)Anti-Alpha-synuclein Reference Antibody (cinpanemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04107-1-sec-hplc.jpgAnti-Alpha-synuclein Reference Antibody (cinpanemab)The purity of Anti-Alpha-synuclein Reference Antibody (cinpanemab)is more than 99.69% https://www.bosterbio.com/catalog/product/view/id/1288512026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04126-sds-page.jpgAnti-SCN11a / Nav1.9 Reference Antibody (Wuhan U. patent anti-Nav1.9)Anti-SCN11a/Nav1.9 Reference Antibody (Wuhan U. patent anti-Nav1.9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04126-sec-hplc.jpgAnti-SCN11a / Nav1.9 Reference Antibody (Wuhan U. patent anti-Nav1.9)The purity of Anti-SCN11a/Nav1.9 Reference Antibody (Wuhan U. patent anti-Nav1.9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288522026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04141-sds-page.jpgAnti-LILRB2 / ILT4 / CD85d Reference Antibody (JTX-8064)Anti-LILRB2/ILT4/CD85d Reference Antibody (JTX-8064) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04141-sec-hplc.jpgAnti-LILRB2 / ILT4 / CD85d Reference Antibody (JTX-8064)The purity of Anti-LILRB2/ILT4/CD85d Reference Antibody (JTX-8064)is more than 98.96%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04141-od450.jpgAnti-LILRB2 / ILT4 / CD85d Reference Antibody (JTX-8064)Immobilized human LILRB2 His at 2 &mug/mL can bind Anti-LILRB2/ILT4/CD85d Reference Antibody (JTX-8064) https://www.bosterbio.com/catalog/product/view/id/1288532026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04175-sds-page.jpgAnti-NKG2A / CD94 Reference Antibody (monalizumab)Anti-NKG2A/CD94 Reference Antibody (monalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04175-sec-hplc.jpgAnti-NKG2A / CD94 Reference Antibody (monalizumab)The purity of Anti-NKG2A/CD94 Reference Antibody (monalizumab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04175-facs.jpgAnti-NKG2A / CD94 Reference Antibody (monalizumab)Human NKG2A/CD94 HEK293 cells were stained with Anti-NKG2A/CD94 Reference Antibody (monalizumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04175-facs-1.jpgAnti-NKG2A / CD94 Reference Antibody (monalizumab)Anti-NKG2A/CD159a Reference Antibody (monalizumab) FACS Blocking was evaluated using human NKG2A/CD94 HEK293 cells. The IC50 was approximately 0.2162 nM. https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04175-luminescence-intensity.jpgAnti-NKG2A / CD94 Reference Antibody (monalizumab)Anti-NKG2A/CD159a Reference Antibody (monalizumab) Luciferase Assay was evaluated using Human NKG2A/CD94 HEK293. The EC50 was approximately 0.5236 nM. https://www.bosterbio.com/catalog/product/view/id/1288542026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04227-4-sds-page.jpgAnti-MADCAM1 Reference Antibody (ontamalimab)Anti-MADCAM1 Reference Antibody (ontamalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04227-4-sec-hplc.jpgAnti-MADCAM1 Reference Antibody (ontamalimab)The purity of Anti-MADCAM1 Reference Antibody (ontamalimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288552026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04237-5-sds-page.jpgAnti-FceR2 / CD23 Reference Antibody (lumiliximab)Anti-FceR2/CD23 Reference Antibody (lumiliximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04237-5-sec-hplc.jpgAnti-FceR2 / CD23 Reference Antibody (lumiliximab)The purity of Anti-FceR2/CD23 Reference Antibody (lumiliximab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288562026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04243-1-sds-page.jpgAnti-IL-5Ra/ CD125 Reference Antibody (benralizumab)Anti-IL-5Ra/ CD125 Reference Antibody (benralizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04243-1-sec-hplc.jpgAnti-IL-5Ra/ CD125 Reference Antibody (benralizumab)The purity of Anti-IL-5Ra/ CD125 Reference Antibody (benralizumab)is more than 98.82%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04243-1-od450.jpgAnti-IL-5Ra/ CD125 Reference Antibody (benralizumab)Immobilized human IL 5Ralpha His at 2 &mug/mL can bind Anti-IL-5Ra/ CD125 Reference Antibody (benralizumab) https://www.bosterbio.com/catalog/product/view/id/1288572026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-1-sds-page.jpgAnti-IL-3Ra / CD123 Reference Antibody (talacotuzumab)Anti-IL-3Ra/CD123 Reference Antibody (talacotuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-1-sec-hplc.jpgAnti-IL-3Ra / CD123 Reference Antibody (talacotuzumab)The purity of Anti-IL-3Ra/CD123 Reference Antibody (talacotuzumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-1-od450.jpgAnti-IL-3Ra / CD123 Reference Antibody (talacotuzumab)Immobilized human IL 3Ralpha His at 2 &mug/mL can bind Anti-IL-3Ra/CD123 Reference Antibody (talacotuzumab) https://www.bosterbio.com/catalog/product/view/id/1288582026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-2-sds-page.jpgAnti-IL-3Ra / CD123 Reference Antibody (talacotuzumab-MMAE)Anti-IL-3Ra/CD123 Reference Antibody (talacotuzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-2-sec-hplc.jpgAnti-IL-3Ra / CD123 Reference Antibody (talacotuzumab-MMAE)The purity of Anti-IL-3Ra/CD123 Reference Antibody (talacotuzumab-MMAE)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-2-od450.jpgAnti-IL-3Ra / CD123 Reference Antibody (talacotuzumab-MMAE)Immobilized human IL 3RA FC at 2 &mug/mL can bind Anti-IL-3Ra/CD123 Reference Antibody (talacotuzumab-MMAE) https://www.bosterbio.com/catalog/product/view/id/1288592026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-3-sds-page.jpgAnti-IL-3Ra / CD123 Reference Antibody (SNG-CD123A)Anti-IL-3Ra/CD123 Reference Antibody (SNG-CD123A) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04307-3-sec-hplc.jpgAnti-IL-3Ra / CD123 Reference Antibody (SNG-CD123A)The purity of Anti-IL-3Ra/CD123 Reference Antibody (SNG-CD123A)is more than 95.78% https://www.bosterbio.com/catalog/product/view/id/1288602026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04332-sds-page.jpgAnti-GUCY2C Reference Antibody (indusatumab)Anti-GUCY2C Reference Antibody (indusatumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04332-sec-hplc.jpgAnti-GUCY2C Reference Antibody (indusatumab)The purity of Anti-GUCY2C Reference Antibody (indusatumab)is more than 98.5%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04332-od450.jpgAnti-GUCY2C Reference Antibody (indusatumab)Immobilized human GUCY2C His at 2 &mug/mL can bind Anti-GUCY2C Reference Antibody (indusatumab) https://www.bosterbio.com/catalog/product/view/id/1288612026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04332-1-sds-page.jpgAnti-GUCY2C Reference Antibody (indusatumab vedotin)Anti-GUCY2C Reference Antibody (indusatumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04332-1-sec-hplc.jpgAnti-GUCY2C Reference Antibody (indusatumab vedotin)The purity of Anti-GUCY2C Reference Antibody (indusatumab vedotin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288622026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04348-2-sds-page.jpgAnti-TNFRSF21 / DR6 / CD358 Reference Antibody (Abbvie patent anti-TNFRSF21)Anti-TNFRSF21/DR6/CD358 Reference Antibody (Abbvie patent anti-TNFRSF21) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04348-2-sec-hplc.jpgAnti-TNFRSF21 / DR6 / CD358 Reference Antibody (Abbvie patent anti-TNFRSF21)The purity of Anti-TNFRSF21/DR6/CD358 Reference Antibody (Abbvie patent anti-TNFRSF21)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288632026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04391-sds-page.jpgAnti-FZD7 Reference Antibody (U.Toronto patent anti-FZD7)Anti-FZD7 Reference Antibody (U.Toronto patent anti-FZD7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04391-sec-hplc.jpgAnti-FZD7 Reference Antibody (U.Toronto patent anti-FZD7)The purity of Anti-FZD7 Reference Antibody (U.Toronto patent anti-FZD7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288642026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04419-sds-page.jpgAnti-CDH11 / Cadherin-11 Reference Antibody (RG6125)Anti-CDH11/Cadherin-11 Reference Antibody (RG6125) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04419-sec-hplc.jpgAnti-CDH11 / Cadherin-11 Reference Antibody (RG6125)The purity of Anti-CDH11/Cadherin-11 Reference Antibody (RG6125)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288652026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04429-sds-page.jpgAnti-IL-25 Reference Antibody (Centocor patent anti-IL-25)Anti-IL-25 Reference Antibody (Centocor patent anti-IL-25) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04429-sec-hplc.jpgAnti-IL-25 Reference Antibody (Centocor patent anti-IL-25)The purity of Anti-IL-25 Reference Antibody (Centocor patent anti-IL-25)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288662026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04432-2-sds-page.jpgAnti-CSF2Ra / GM-CSFRa / CD116 Reference Antibody (mavrilimumab)Anti-CSF2Ra/GM-CSFRa/CD116 Reference Antibody (mavrilimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04432-2-sec-hplc.jpgAnti-CSF2Ra / GM-CSFRa / CD116 Reference Antibody (mavrilimumab)The purity of Anti-CSF2Ra/GM-CSFRa/CD116 Reference Antibody (mavrilimumab)is more than 96.17%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04432-2-od450.jpgAnti-CSF2Ra / GM-CSFRa / CD116 Reference Antibody (mavrilimumab)Immobilized human CD116 His at 2 &mug/mL can bind Anti-CSF2Ra/GM-CSFRa/CD116 Reference Antibody (mavrilimumab) https://www.bosterbio.com/catalog/product/view/id/1288672026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04494-3-sds-page.jpgAnti-VEGFB Reference Antibody (CSL346)Anti-VEGFB Reference Antibody (CSL346) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04494-3-sec-hplc.jpgAnti-VEGFB Reference Antibody (CSL346)The purity of Anti-VEGFB Reference Antibody (CSL346)is more than 98.5% https://www.bosterbio.com/catalog/product/view/id/1288682026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04527-2-sds-page.jpgAnti-IL-13Ra1 / CD213a1 Reference Antibody (MK-6105)Anti-IL-13Ra1/CD213a1 Reference Antibody (MK-6105) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04527-2-sec-hplc.jpgAnti-IL-13Ra1 / CD213a1 Reference Antibody (MK-6105)The purity of Anti-IL-13Ra1/CD213a1 Reference Antibody (MK-6105)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288692026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04653-1-sds-page.jpgAnti-ACVR2B Reference Antibody (bimagrumab)Anti-ACVR2B Reference Antibody (bimagrumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04653-1-sec-hplc.jpgAnti-ACVR2B Reference Antibody (bimagrumab)The purity of Anti-ACVR2B Reference Antibody (bimagrumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04653-1-od450.jpgAnti-ACVR2B Reference Antibody (bimagrumab)Immobilized human ACVR2B chis at 2 &mug/mL can bind Anti-ACVR2B Reference Antibody (bimagrumab) https://www.bosterbio.com/catalog/product/view/id/1288702026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04653-2-sds-page.jpgAnti-ACVR2B Reference Antibody (Acceleron patent anti-ActRIIB)Anti-ACVR2B Reference Antibody (Acceleron patent anti-ActRIIB) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04653-2-sec-hplc.jpgAnti-ACVR2B Reference Antibody (Acceleron patent anti-ActRIIB)The purity of Anti-ACVR2B Reference Antibody (Acceleron patent anti-ActRIIB)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288712026-03-10T04:39:32+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04735-1-sds-page.jpgAnti-TEM1 / Endosialin / CD248 Reference Antibody (ontuxizumab)Anti-TEM1/Endosialin/CD248 Reference Antibody (ontuxizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04735-1-sec-hplc.jpgAnti-TEM1 / Endosialin / CD248 Reference Antibody (ontuxizumab)The purity of Anti-TEM1/Endosialin/CD248 Reference Antibody (ontuxizumab)is more than 99.57% https://www.bosterbio.com/catalog/product/view/id/1288722026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04770-2-sds-page.jpgAnti-ACVR2A Reference Antibody (Ab-14E1)Anti-ACVR2A Reference Antibody (Ab-14E1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04770-2-sec-hplc.jpgAnti-ACVR2A Reference Antibody (Ab-14E1)The purity of Anti-ACVR2A Reference Antibody (Ab-14E1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288732026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04849-sds-page.jpgAnti-CLEC12A / CD371 Reference Antibody (tepoditamab)Anti-CLEC12A/CD371 Reference Antibody (tepoditamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04849-sec-hplc.jpgAnti-CLEC12A / CD371 Reference Antibody (tepoditamab)The purity of Anti-CLEC12A/CD371 Reference Antibody (tepoditamab)is more than 98.77% https://www.bosterbio.com/catalog/product/view/id/1288742026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04924-sds-page.jpgAnti-LILRB4 / ILT3 / CD85k Reference Antibody (Merck patent anti-ILT3 complex)Anti-LILRB4/ILT3/CD85k Reference Antibody (Merck patent anti-ILT3 complex) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04924-sec-hplc.jpgAnti-LILRB4 / ILT3 / CD85k Reference Antibody (Merck patent anti-ILT3 complex)The purity of Anti-LILRB4/ILT3/CD85k Reference Antibody (Merck patent anti-ILT3 complex)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288752026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04924-1-sds-page.jpgAnti-LILRB4 / ILT3 / CD85k Reference Antibody (U.Texas patent anti-LILRB4)Anti-LILRB4/ILT3/CD85k Reference Antibody (U.Texas patent anti-LILRB4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04924-1-sec-hplc.jpgAnti-LILRB4 / ILT3 / CD85k Reference Antibody (U.Texas patent anti-LILRB4)The purity of Anti-LILRB4/ILT3/CD85k Reference Antibody (U.Texas patent anti-LILRB4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288762026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04939-sds-page.jpgAnti-CD93 Reference Antibody (Dcby02)Anti-CD93 Reference Antibody (Dcby02) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04939-sec-hplc.jpgAnti-CD93 Reference Antibody (Dcby02)The purity of Anti-CD93 Reference Antibody (Dcby02)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288772026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04984-3-sds-page.jpgAnti-RGMA Reference Antibody (elezanumab)Anti-RGMA Reference Antibody (elezanumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m04984-3-sec-hplc.jpgAnti-RGMA Reference Antibody (elezanumab)The purity of Anti-RGMA Reference Antibody (elezanumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288782026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05124-2-sds-page.jpgAnti-IL-20 Reference Antibody (fletikumab)Anti-IL-20 Reference Antibody (fletikumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05124-2-sec-hplc.jpgAnti-IL-20 Reference Antibody (fletikumab)The purity of Anti-IL-20 Reference Antibody (fletikumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288792026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05124-3-sds-page.jpgAnti-IL-20 Reference Antibody (Cheng Kung U. patent anti-IL-20)Anti-IL-20 Reference Antibody (Cheng Kung U. patent anti-IL-20) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05124-3-sec-hplc.jpgAnti-IL-20 Reference Antibody (Cheng Kung U. patent anti-IL-20)The purity of Anti-IL-20 Reference Antibody (Cheng Kung U. patent anti-IL-20)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288802026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05151-3-sds-page.jpgAnti-SIRPa / CD172a Reference Antibody (Hospital for Sick Children patent anti-SIRPA)Anti-SIRPa/CD172a Reference Antibody (Hospital for Sick Children patent anti-SIRPA) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05151-3-sec-hplc.jpgAnti-SIRPa / CD172a Reference Antibody (Hospital for Sick Children patent anti-SIRPA)The purity of Anti-SIRPa/CD172a Reference Antibody (Hospital for Sick Children patent anti-SIRPA)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05151-3-od450.jpgAnti-SIRPa / CD172a Reference Antibody (Hospital for Sick Children patent anti-SIRPA)Immobilized human SIRPalpha V1 FC at4 &mug/mL can bind Anti-SIRPa/CD172a Reference Antibody (Hospital for Sick Children patent anti-SIRPA)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05151-3-facs.jpgAnti-SIRPa / CD172a Reference Antibody (Hospital for Sick Children patent anti-SIRPA)Hospital for Sick Children patent anti-SIRPA FACS Blocking was evaluated using human CCRF-CEM cells. The IC50 was approximately 3.289 ug/ml. https://www.bosterbio.com/catalog/product/view/id/1288812026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05151-4-sds-page.jpgAnti-SIRPa / CD172a Reference Antibody (BI 765063)Anti-SIRPa/CD172a Reference Antibody (BI 765063) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05151-4-sec-hplc.jpgAnti-SIRPa / CD172a Reference Antibody (BI 765063)The purity of Anti-SIRPa/CD172a Reference Antibody (BI 765063)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288822026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05178-sds-page.jpgAnti-CAPRIN1 Reference Antibody (Toray patent anti-Caprin-1)Anti-CAPRIN1 Reference Antibody (Toray patent anti-Caprin-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05178-sec-hplc.jpgAnti-CAPRIN1 Reference Antibody (Toray patent anti-Caprin-1)The purity of Anti-CAPRIN1 Reference Antibody (Toray patent anti-Caprin-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288832026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05256-sds-page.jpgAnti-IL-31Ra Reference Antibody (nemolizumab)Anti-IL-31Ra Reference Antibody (nemolizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05256-sec-hplc.jpgAnti-IL-31Ra Reference Antibody (nemolizumab)The purity of Anti-IL-31Ra Reference Antibody (nemolizumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05256-od450.jpgAnti-IL-31Ra Reference Antibody (nemolizumab)Immobilized human IL31R His at 2 &mug/mL can bind Anti-IL-31Ra Reference Antibody (nemolizumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05256-facs.jpgAnti-IL-31Ra Reference Antibody (nemolizumab)Human IL31R HEK293 cells were stained with Anti-IL-31Ra Reference Antibody (nemolizumab) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05256-facs-1.jpgAnti-IL-31Ra Reference Antibody (nemolizumab)Anti-IL-31Ra Reference Antibody (nemolizumab) P-STAT3 Assay was evaluated using Du145. The IC50 was approximately 0.1068 ug/ml.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05256-il-6.jpgAnti-IL-31Ra Reference Antibody (nemolizumab)Anti-IL-31Ra Reference Antibody (nemolizumab) Activation inhibition was evaluated using Hacat. The max induction fold was approximately 1.86. https://www.bosterbio.com/catalog/product/view/id/1288842026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-sds-page.jpgAnti-TSPAN26 / CD37 Reference Antibody (naratuximab)Anti-TSPAN26/CD37 Reference Antibody (naratuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-sec-hplc.jpgAnti-TSPAN26 / CD37 Reference Antibody (naratuximab)The purity of Anti-TSPAN26/CD37 Reference Antibody (naratuximab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-od450.jpgAnti-TSPAN26 / CD37 Reference Antibody (naratuximab)Immobilized human CD37 VLP at16 &mug/mL can bind Anti-TSPAN26/CD37 Reference Antibody (naratuximab) https://www.bosterbio.com/catalog/product/view/id/1288852026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-1-sds-page.jpgAnti-TSPAN26 / CD37 Reference Antibody (AGS67E)Anti-TSPAN26/CD37 Reference Antibody (AGS67E) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-1-sec-hplc.jpgAnti-TSPAN26 / CD37 Reference Antibody (AGS67E)The purity of Anti-TSPAN26/CD37 Reference Antibody (AGS67E)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288862026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-2-sds-page.jpgAnti-TSPAN26 / CD37 Reference Antibody (lilotomab)Anti-TSPAN26/CD37 Reference Antibody (lilotomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-2-sec-hplc.jpgAnti-TSPAN26 / CD37 Reference Antibody (lilotomab)The purity of Anti-TSPAN26/CD37 Reference Antibody (lilotomab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288872026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-3-sds-page.jpgAnti-TSPAN26 / CD37 Reference Antibody (otlertuzumab)Anti-TSPAN26/CD37 Reference Antibody (otlertuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05276-3-sec-hplc.jpgAnti-TSPAN26 / CD37 Reference Antibody (otlertuzumab)The purity of Anti-TSPAN26/CD37 Reference Antibody (otlertuzumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288882026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05310-sds-page.jpgAnti-SLAMF6 / CD352 Reference Antibody (SGN-CD352A)Anti-SLAMF6/CD352 Reference Antibody (SGN-CD352A) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05310-sec-hplc.jpgAnti-SLAMF6 / CD352 Reference Antibody (SGN-CD352A)The purity of Anti-SLAMF6/CD352 Reference Antibody (SGN-CD352A)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288892026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05387-2-sds-page.jpgAnti-RSPO3 Reference Antibody (rosmantuzumab)Anti-RSPO3 Reference Antibody (rosmantuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05387-2-sec-hplc.jpgAnti-RSPO3 Reference Antibody (rosmantuzumab)The purity of Anti-RSPO3 Reference Antibody (rosmantuzumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1288902026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05433-1-sds-page.jpgAnti-Integrin b7 / ITGB7 Reference Antibody (Genentech patent anti-Integrin beta7)Anti-Integrin b7/ITGB7 Reference Antibody (Genentech patent anti-Integrin beta7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05433-1-sec-hplc.jpgAnti-Integrin b7 / ITGB7 Reference Antibody (Genentech patent anti-Integrin beta7)The purity of Anti-Integrin b7/ITGB7 Reference Antibody (Genentech patent anti-Integrin beta7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288912026-03-10T04:39:33+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05505-sds-page.jpgAnti-STAB1 Reference Antibody (bexmarilimab)Anti-STAB1 Reference Antibody (bexmarilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05505-sec-hplc.jpgAnti-STAB1 Reference Antibody (bexmarilimab)The purity of Anti-STAB1 Reference Antibody (bexmarilimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05505-od450.jpgAnti-STAB1 Reference Antibody (bexmarilimab)Immobilized human STAB His at 2 &mug/mL can bind Anti-STAB1 Reference Antibody (bexmarilimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05505-facs.jpgAnti-STAB1 Reference Antibody (bexmarilimab)Human STAB A4 HEK293 cells were stained with Anti-STAB1 Reference Antibody (bexmarilimab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1288922026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05615-1-sds-page.jpgAnti-ENPP3 / CD203c Reference Antibody (Ags-16C3F)Anti-ENPP3/CD203c Reference Antibody (Ags-16C3F) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05615-1-sec-hplc.jpgAnti-ENPP3 / CD203c Reference Antibody (Ags-16C3F)The purity of Anti-ENPP3/CD203c Reference Antibody (Ags-16C3F)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288932026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05625-1-sds-page.jpgAnti-Phosphatidylserine Reference Antibody (bavituximab)Anti-Phosphatidylserine Reference Antibody (bavituximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05625-1-sec-hplc.jpgAnti-Phosphatidylserine Reference Antibody (bavituximab)The purity of Anti-Phosphatidylserine Reference Antibody (bavituximab)is more than 98.38% https://www.bosterbio.com/catalog/product/view/id/1288942026-03-25T05:25:00+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05632-sds-page.jpgAnti-RAMP3 Reference Antibody (Medella patent anti-RAMP-3)Anti-RAMP3 Reference Antibody (Medella patent anti-RAMP-3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05632-sec-hplc.jpgAnti-RAMP3 Reference Antibody (Medella patent anti-RAMP-3)The purity of Anti-RAMP3 Reference Antibody (Medella patent anti-RAMP-3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1288952026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05693-sds-page.jpgAnti-LIV-1 / SLC39A6 Reference Antibody (ladiratuzumAb)Anti-LIV-1/SLC39A6 Reference Antibody (ladiratuzumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05693-sec-hplc.jpgAnti-LIV-1 / SLC39A6 Reference Antibody (ladiratuzumAb)The purity of Anti-LIV-1/SLC39A6 Reference Antibody (ladiratuzumAb)is more than 98.2%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05693-od450.jpgAnti-LIV-1 / SLC39A6 Reference Antibody (ladiratuzumAb)Immobilized human LIV 1 His at 2 &mug/mL can bind Anti-LIV-1/SLC39A6 Reference Antibody (ladiratuzumAb) https://www.bosterbio.com/catalog/product/view/id/1288962026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05693-1-sds-page.jpgAnti-LIV-1 / SLC39A6 Reference Antibody ((ladiratuzumab vedotin)Anti-LIV-1/SLC39A6 Reference Antibody ((ladiratuzumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05693-1-sec-hplc.jpgAnti-LIV-1 / SLC39A6 Reference Antibody ((ladiratuzumab vedotin)The purity of Anti-LIV-1/SLC39A6 Reference Antibody ((ladiratuzumab vedotin)is more than 98.2%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05693-1-od450.jpgAnti-LIV-1 / SLC39A6 Reference Antibody ((ladiratuzumab vedotin)Immobilized human LIV 1https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05693-1-facs.jpgAnti-LIV-1 / SLC39A6 Reference Antibody ((ladiratuzumab vedotin)Human LIV1 CHOS cells were stained with Anti-LIV-1/SLC39A6 Reference Antibody ((ladiratuzumab vedotin) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1288972026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05705-sds-page.jpgAnti-IL-22Ra Reference Antibody (ARGX-112)Anti-IL-22Ra Reference Antibody (ARGX-112) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05705-sec-hplc.jpgAnti-IL-22Ra Reference Antibody (ARGX-112)The purity of Anti-IL-22Ra Reference Antibody (ARGX-112)is more than 98.11% https://www.bosterbio.com/catalog/product/view/id/1288982026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-sds-page.jpgAnti-DLL3 Reference Antibody (rovalpituzumab)Anti-DLL3 Reference Antibody (rovalpituzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-sec-hplc.jpgAnti-DLL3 Reference Antibody (rovalpituzumab)The purity of Anti-DLL3 Reference Antibody (rovalpituzumab)is more than 98.44%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-od450.jpgAnti-DLL3 Reference Antibody (rovalpituzumab)Immobilized human DLL3 His at 2 &mug/mL can bind Anti-DLL3 Reference Antibody (rovalpituzumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-facs.jpgAnti-DLL3 Reference Antibody (rovalpituzumab)Human DLL3 HEK293 cells were stained with Anti-DLL3 Reference Antibody (rovalpituzumab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1288992026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-1-sds-page.jpgAnti-DLL3 Reference Antibody (rovalpituzumab-MMAE)Anti-DLL3 Reference Antibody (rovalpituzumab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-1-sec-hplc.jpgAnti-DLL3 Reference Antibody (rovalpituzumab-MMAE)The purity of Anti-DLL3 Reference Antibody (rovalpituzumab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289002026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-2-sds-page.jpgAnti-DLL3 Reference Antibody (Dragonfly patent anti-DLL3)Anti-DLL3 Reference Antibody (Dragonfly patent anti-DLL3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05871-2-sec-hplc.jpgAnti-DLL3 Reference Antibody (Dragonfly patent anti-DLL3)The purity of Anti-DLL3 Reference Antibody (Dragonfly patent anti-DLL3)is more than 95.49% https://www.bosterbio.com/catalog/product/view/id/1289012026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05877-sds-page.jpgAnti-Klotho Beta Reference Antibody (NGM313)Anti-Klotho Beta Reference Antibody (NGM313) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05877-sec-hplc.jpgAnti-Klotho Beta Reference Antibody (NGM313)The purity of Anti-Klotho Beta Reference Antibody (NGM313)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289022026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05877-1-sds-page.jpgAnti-Klotho Beta Reference Antibody (RG7992)Anti-Klotho Beta Reference Antibody (RG7992) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05877-1-sec-hplc.jpgAnti-Klotho Beta Reference Antibody (RG7992)The purity of Anti-Klotho Beta Reference Antibody (RG7992)is more than 95.82% https://www.bosterbio.com/catalog/product/view/id/1289032026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05914-sds-page.jpgAnti-PGLYRP1 / PGRP-S Reference Antibody (Novo Nordisk patent anti-PGLYRP1)Anti-PGLYRP1/PGRP-S Reference Antibody (Novo Nordisk patent anti-PGLYRP1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m05914-sec-hplc.jpgAnti-PGLYRP1 / PGRP-S Reference Antibody (Novo Nordisk patent anti-PGLYRP1)The purity of Anti-PGLYRP1/PGRP-S Reference Antibody (Novo Nordisk patent anti-PGLYRP1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289042026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06002-4-sds-page.jpgAnti-IDO2 Reference Antibody (LIMR patent anti-IDO2)Anti-IDO2 Reference Antibody (LIMR patent anti-IDO2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06002-4-sec-hplc.jpgAnti-IDO2 Reference Antibody (LIMR patent anti-IDO2)The purity of Anti-IDO2 Reference Antibody (LIMR patent anti-IDO2)is more than 97.85% https://www.bosterbio.com/catalog/product/view/id/1289052026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06032-2-sds-page.jpgAnti-TNFSF9 / 4-1BBL Reference Antibody (Abbvie patent anti-TNFSF9)Anti-TNFSF9/4-1BBL Reference Antibody (Abbvie patent anti-TNFSF9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06032-2-sec-hplc.jpgAnti-TNFSF9 / 4-1BBL Reference Antibody (Abbvie patent anti-TNFSF9)The purity of Anti-TNFSF9/4-1BBL Reference Antibody (Abbvie patent anti-TNFSF9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289062026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06043-sds-page.jpgAnti-PAC1 Reference Antibody (zelminemab)Anti-PAC1 Reference Antibody (zelminemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06043-sec-hplc.jpgAnti-PAC1 Reference Antibody (zelminemab)The purity of Anti-PAC1 Reference Antibody (zelminemab)is more than 99.15% https://www.bosterbio.com/catalog/product/view/id/1289072026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06105-sds-page.jpgAnti-IL-13Ra2 / CD213a2 Reference Antibody (Wake Forest U. patent anti-IL-13RA2)Anti-IL-13Ra2/CD213a2 Reference Antibody (Wake Forest U. patent anti-IL-13RA2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06105-sec-hplc.jpgAnti-IL-13Ra2 / CD213a2 Reference Antibody (Wake Forest U. patent anti-IL-13RA2)The purity of Anti-IL-13Ra2/CD213a2 Reference Antibody (Wake Forest U. patent anti-IL-13RA2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289082026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06219-sds-page.jpgAnti-GM3 Reference Antibody (racotumomab)Anti-GM3 Reference Antibody (racotumomab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06219-sec-hplc.jpgAnti-GM3 Reference Antibody (racotumomab)The purity of Anti-GM3 Reference Antibody (racotumomab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289092026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-3-sds-page.jpgAnti-TNFRSF12A / TWEAKR / CD266 Reference Antibody (enavatuzumab)Anti-TNFRSF12A/TWEAKR/CD266 Reference Antibody (enavatuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06261-3-sec-hplc.jpgAnti-TNFRSF12A / TWEAKR / CD266 Reference Antibody (enavatuzumab)The purity of Anti-TNFRSF12A/TWEAKR/CD266 Reference Antibody (enavatuzumab)is more than 98.7% https://www.bosterbio.com/catalog/product/view/id/1289102026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-1-sds-page.jpgAnti-CDH6 / K-Cadherin Reference Antibody (HKT288)Anti-CDH6/K-Cadherin Reference Antibody (HKT288) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-1-sec-hplc.jpgAnti-CDH6 / K-Cadherin Reference Antibody (HKT288)The purity of Anti-CDH6/K-Cadherin Reference Antibody (HKT288)is more than 97.93%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-1-od450.jpgAnti-CDH6 / K-Cadherin Reference Antibody (HKT288)Immobilized Cyno CDH6 His at 2 &mug/mL can bind Anti-CDH6/K-Cadherin Reference Antibody (HKT288)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-1-facs.jpgAnti-CDH6 / K-Cadherin Reference Antibody (HKT288)Human CDH6 HEK293(A6) cells were stained with Anti-CDH6/K-Cadherin Reference Antibody (HKT288) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-1-internalization-rate.jpgAnti-CDH6 / K-Cadherin Reference Antibody (HKT288)The endocytosis ratio HKT288 by Hu-CDH6-HEK293(A6) increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-1-luminescence-intensity.jpgAnti-CDH6 / K-Cadherin Reference Antibody (HKT288)HKT288 induced OVCAR3 Luciferase activity was evaluated using huCD16a(V158)-NF-AT-Jurkat Reporter Cell. The EC50 was approximately 0.6792 nM. https://www.bosterbio.com/catalog/product/view/id/1289112026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-2-sds-page.jpgAnti-CDH6 / K-Cadherin Reference Antibody (DS-6000a)Anti-CDH6/K-Cadherin Reference Antibody (DS-6000a) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06353-2-sec-hplc.jpgAnti-CDH6 / K-Cadherin Reference Antibody (DS-6000a)The purity of Anti-CDH6/K-Cadherin Reference Antibody (DS-6000a)is more than 98.75% https://www.bosterbio.com/catalog/product/view/id/1289122026-03-10T04:39:34+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-1-sds-page.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (10C12)Anti-CDH17/Cadherin-17 Reference Antibody (10C12) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-1-sec-hplc.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (10C12)The purity of Anti-CDH17/Cadherin-17 Reference Antibody (10C12)is more than 98.15%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-1-od450.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (10C12)Immobilized human CDH17https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-1-facs.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (10C12)Human CDH17 HEK293 cells were stained with Anti-CDH17/Cadherin-17 Reference Antibody (10C12) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-1-internalization-rate.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (10C12)The endocytosis ratio 10C12 by Human CDH17 HEK293 increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-1-xenograft-colo205-cell-model.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (10C12)10C12 inhibited the tumor growth of COLO205 on nude mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1289132026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-2-sds-page.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (PTA001_A4)Anti-CDH17/Cadherin-17 Reference Antibody (PTA001_A4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06389-2-sec-hplc.jpgAnti-CDH17 / Cadherin-17 Reference Antibody (PTA001_A4)The purity of Anti-CDH17/Cadherin-17 Reference Antibody (PTA001_A4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289142026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06402-sds-page.jpgAnti-Dysadherin Reference Antibody (Centrose patent anti-dysadherin)Anti-Dysadherin Reference Antibody (Centrose patent anti-dysadherin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06402-sec-hplc.jpgAnti-Dysadherin Reference Antibody (Centrose patent anti-dysadherin)The purity of Anti-Dysadherin Reference Antibody (Centrose patent anti-dysadherin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289152026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06435-sds-page.jpgAnti- FcRH5 / IRTA2 / CD307e Reference Antibody (cevostamab)Anti- FcRH5/IRTA2/CD307e Reference Antibody (cevostamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06435-sec-hplc.jpgAnti- FcRH5 / IRTA2 / CD307e Reference Antibody (cevostamab)The purity of Anti- FcRH5/IRTA2/CD307e Reference Antibody (cevostamab)is more than 91.59%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06435-od450.jpgAnti- FcRH5 / IRTA2 / CD307e Reference Antibody (cevostamab)Immobilized human IRTA2 His at 2 &mug/mL can bind Anti- FcRH5/IRTA2/CD307e Reference Antibody (cevostamab) https://www.bosterbio.com/catalog/product/view/id/1289162026-03-24T05:33:57+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06435-1-sds-page.jpgAnti- FcRH5 / IRTA2 / CD307e Reference Antibody (DFRF4539A)Anti- FcRH5/IRTA2/CD307e Reference Antibody (DFRF4539A) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06435-1-sec-hplc.jpgAnti- FcRH5 / IRTA2 / CD307e Reference Antibody (DFRF4539A)The purity of Anti- FcRH5/IRTA2/CD307e Reference Antibody (DFRF4539A)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289172026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06628-sds-page.jpgAnti-PRAME Reference Antibody (Eureka patent anti-PRAME)Anti-PRAME Reference Antibody (Eureka patent anti-PRAME) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06628-sec-hplc.jpgAnti-PRAME Reference Antibody (Eureka patent anti-PRAME)The purity of Anti-PRAME Reference Antibody (Eureka patent anti-PRAME)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289182026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06629-sds-page.jpgAnti-DCSTAMP Reference Antibody (U.Rochester patent anti-DC-STAMP)Anti-DCSTAMP Reference Antibody (U.Rochester patent anti-DC-STAMP) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06629-sec-hplc.jpgAnti-DCSTAMP Reference Antibody (U.Rochester patent anti-DC-STAMP)The purity of Anti-DCSTAMP Reference Antibody (U.Rochester patent anti-DC-STAMP)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289192026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06641-1-sds-page.jpgAnti-SLC2A8 Reference Antibody (VB1-050)Anti-SLC2A8 Reference Antibody (VB1-050) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06641-1-sec-hplc.jpgAnti-SLC2A8 Reference Antibody (VB1-050)The purity of Anti-SLC2A8 Reference Antibody (VB1-050)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289202026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06738-sds-page.jpgAnti-PLA2G1B Reference Antibody (Diaccurate patent anti-sPLA2-GIB)Anti-PLA2G1B Reference Antibody (Diaccurate patent anti-sPLA2-GIB) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06738-sec-hplc.jpgAnti-PLA2G1B Reference Antibody (Diaccurate patent anti-sPLA2-GIB)The purity of Anti-PLA2G1B Reference Antibody (Diaccurate patent anti-sPLA2-GIB)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289212026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06777-1-sds-page.jpgAnti-INHBA / Activin A Reference Antibody (garetosmab)Anti-INHBA/Activin A Reference Antibody (garetosmab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06777-1-sec-hplc.jpgAnti-INHBA / Activin A Reference Antibody (garetosmab)The purity of Anti-INHBA/Activin A Reference Antibody (garetosmab)is more than 91.47% https://www.bosterbio.com/catalog/product/view/id/1289222026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06997-sds-page.jpgAnti-TSPAN8 Reference Antibody (INSERM patent anti-CO-029)Anti-TSPAN8 Reference Antibody (INSERM patent anti-CO-029) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m06997-sec-hplc.jpgAnti-TSPAN8 Reference Antibody (INSERM patent anti-CO-029)The purity of Anti-TSPAN8 Reference Antibody (INSERM patent anti-CO-029)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289232026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-7-sds-page.jpgAnti-Histone H2B Reference Antibody (Immunomedics patent anti-Histone H2B)Anti-Histone H2B Reference Antibody (Immunomedics patent anti-Histone H2B) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07286-7-sec-hplc.jpgAnti-Histone H2B Reference Antibody (Immunomedics patent anti-Histone H2B)The purity of Anti-Histone H2B Reference Antibody (Immunomedics patent anti-Histone H2B)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289242026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07313-sds-page.jpgAnti-CLEC4C Reference Antibody (BIIB059)Anti-CLEC4C Reference Antibody (BIIB059) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07313-sec-hplc.jpgAnti-CLEC4C Reference Antibody (BIIB059)The purity of Anti-CLEC4C Reference Antibody (BIIB059)is more than 99.42%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07313-od450.jpgAnti-CLEC4C Reference Antibody (BIIB059)Immobilized Ma CLEC4C His at 2 &mug/mL can bind Anti-CLEC4C Reference Antibody (BIIB059) https://www.bosterbio.com/catalog/product/view/id/1289252026-03-10T04:39:35+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07313-1-sds-page.jpgAnti-CLEC4C Reference Antibody (LFB patent anti-BDCA-2)Anti-CLEC4C Reference Antibody (LFB patent anti-BDCA-2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07313-1-sec-hplc.jpgAnti-CLEC4C Reference Antibody (LFB patent anti-BDCA-2)The purity of Anti-CLEC4C Reference Antibody (LFB patent anti-BDCA-2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289262026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07399-sds-page.jpgAnti-TPSAB1 Reference Antibody (Genentech patent anti-Tryptase Beta 1)Anti-TPSAB1 Reference Antibody (Genentech patent anti-Tryptase Beta 1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07399-sec-hplc.jpgAnti-TPSAB1 Reference Antibody (Genentech patent anti-Tryptase Beta 1)The purity of Anti-TPSAB1 Reference Antibody (Genentech patent anti-Tryptase Beta 1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289272026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-2-sds-page.jpgAnti-TPBG Reference Antibody (PF-06263507)Anti-TPBG Reference Antibody (PF-06263507) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-2-sec-hplc.jpgAnti-TPBG Reference Antibody (PF-06263507)The purity of Anti-TPBG Reference Antibody (PF-06263507)is more than 99.25%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-2-od450.jpgAnti-TPBG Reference Antibody (PF-06263507)Immobilized human 5T4 His at 2 &mug/mL can bind Anti-TPBG Reference Antibody (PF-06263507)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-2-facs.jpgAnti-TPBG Reference Antibody (PF-06263507)Human 5T4 HEK293 cells were stained with Anti-TPBG Reference Antibody (PF-06263507) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1289282026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-3-sds-page.jpgAnti-TPBG Reference Antibody (naptumomAb)Anti-TPBG Reference Antibody (naptumomAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-3-sec-hplc.jpgAnti-TPBG Reference Antibody (naptumomAb)The purity of Anti-TPBG Reference Antibody (naptumomAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289292026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-4-sds-page.jpgAnti-TPBG Reference Antibody (ASN004)Anti-TPBG Reference Antibody (ASN004) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-4-sec-hplc.jpgAnti-TPBG Reference Antibody (ASN004)The purity of Anti-TPBG Reference Antibody (ASN004)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289302026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-5-sds-page.jpgAnti-TPBG Reference Antibody (Wyeth patent anti-5T4)Anti-TPBG Reference Antibody (Wyeth patent anti-5T4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07442-5-sec-hplc.jpgAnti-TPBG Reference Antibody (Wyeth patent anti-5T4)The purity of Anti-TPBG Reference Antibody (Wyeth patent anti-5T4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289312026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07481-sds-page.jpgAnti-GFRA3 Reference Antibody (nadecnemab)Anti-GFRA3 Reference Antibody (nadecnemab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07481-sec-hplc.jpgAnti-GFRA3 Reference Antibody (nadecnemab)The purity of Anti-GFRA3 Reference Antibody (nadecnemab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289322026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07506-sds-page.jpgAnti-STEAP1 Reference Antibody (vandortuzumAb)Anti-STEAP1 Reference Antibody (vandortuzumAb) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07506-sec-hplc.jpgAnti-STEAP1 Reference Antibody (vandortuzumAb)The purity of Anti-STEAP1 Reference Antibody (vandortuzumAb)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289332026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07549-sds-page.jpgAnti-FZD10 Reference Antibody (tabituximab)Anti-FZD10 Reference Antibody (tabituximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07549-sec-hplc.jpgAnti-FZD10 Reference Antibody (tabituximab)The purity of Anti-FZD10 Reference Antibody (tabituximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289342026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07619-sds-page.jpgAnti-Sphingosine-1-phosphate Reference Antibody (sonepcizumab)Anti-Sphingosine-1-phosphate Reference Antibody (sonepcizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07619-sec-hplc.jpgAnti-Sphingosine-1-phosphate Reference Antibody (sonepcizumab)The purity of Anti-Sphingosine-1-phosphate Reference Antibody (sonepcizumab)is more than 98.9% https://www.bosterbio.com/catalog/product/view/id/1289352026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07619-1-sds-page.jpgAnti-Sphingosine-1-phosphate Reference Antibody (Expression DD patent anti-SIP)Anti-Sphingosine-1-phosphate Reference Antibody (Expression DD patent anti-SIP) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07619-1-sec-hplc.jpgAnti-Sphingosine-1-phosphate Reference Antibody (Expression DD patent anti-SIP)The purity of Anti-Sphingosine-1-phosphate Reference Antibody (Expression DD patent anti-SIP)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289362026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07688-2-sds-page.jpgAnti-GPA33 Reference Antibody (KRN330)Anti-GPA33 Reference Antibody (KRN330) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07688-2-sec-hplc.jpgAnti-GPA33 Reference Antibody (KRN330)The purity of Anti-GPA33 Reference Antibody (KRN330)is more than 98.84% https://www.bosterbio.com/catalog/product/view/id/1289372026-03-10T04:39:36+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07783-sds-page.jpgAnti-MUC17 Reference Antibody (Forerunner patent anti-Muc 17)Anti-MUC17 Reference Antibody (Forerunner patent anti-Muc 17) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07783-sec-hplc.jpgAnti-MUC17 Reference Antibody (Forerunner patent anti-Muc 17)The purity of Anti-MUC17 Reference Antibody (Forerunner patent anti-Muc 17)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289382026-03-10T04:39:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07820-1-sds-page.jpgAnti-Integrin a11 / ITAG11 Reference Antibody (Scripps patent anti-CD11a)Anti-Integrin a11/ITAG11 Reference Antibody (Scripps patent anti-CD11a) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07820-1-sec-hplc.jpgAnti-Integrin a11 / ITAG11 Reference Antibody (Scripps patent anti-CD11a)The purity of Anti-Integrin a11/ITAG11 Reference Antibody (Scripps patent anti-CD11a)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289392026-03-10T04:39:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07964-sds-page.jpgAnti-Nectin-4 Reference Antibody (enfortumab vedotin-ejfv)Anti-Nectin-4 Reference Antibody (enfortumab vedotin-ejfv) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07964-sec-hplc.jpgAnti-Nectin-4 Reference Antibody (enfortumab vedotin-ejfv)The purity of Anti-Nectin-4 Reference Antibody (enfortumab vedotin-ejfv)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07964-od450.jpgAnti-Nectin-4 Reference Antibody (enfortumab vedotin-ejfv)Immobilized human NECTIN 4 His at 2 &mug/mL can bind Anti-Nectin-4 Reference Antibody (enfortumab vedotin-ejfv) https://www.bosterbio.com/catalog/product/view/id/1289402026-03-10T04:39:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07964-1-sds-page.jpgAnti-Nectin-4 Reference Antibody (enfortumab)Anti-Nectin-4 Reference Antibody (enfortumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07964-1-sec-hplc.jpgAnti-Nectin-4 Reference Antibody (enfortumab)The purity of Anti-Nectin-4 Reference Antibody (enfortumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m07964-1-od450.jpgAnti-Nectin-4 Reference Antibody (enfortumab)Immobilized human NECTIN 4 His at 2 &mug/mL can bind Anti-Nectin-4 Reference Antibody (enfortumab) https://www.bosterbio.com/catalog/product/view/id/1289412026-03-10T04:39:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08008-sds-page.jpgAnti-SLC44A4 Reference Antibody (ASG-5ME)Anti-SLC44A4 Reference Antibody (ASG-5ME) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08008-sec-hplc.jpgAnti-SLC44A4 Reference Antibody (ASG-5ME)The purity of Anti-SLC44A4 Reference Antibody (ASG-5ME)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289422026-03-10T04:39:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08105-sds-page.jpgAnti-CRTAM / CD355 Reference Antibody (Oxford Bio patent anti-CRTAM)Anti-CRTAM/CD355 Reference Antibody (Oxford Bio patent anti-CRTAM) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08105-sec-hplc.jpgAnti-CRTAM / CD355 Reference Antibody (Oxford Bio patent anti-CRTAM)The purity of Anti-CRTAM/CD355 Reference Antibody (Oxford Bio patent anti-CRTAM)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289432026-03-10T04:39:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-3-sds-page.jpgAnti-CLDN6 Reference Antibody (AB3-7)Anti-CLDN6 Reference Antibody (AB3-7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-3-sec-hplc.jpgAnti-CLDN6 Reference Antibody (AB3-7)The purity of Anti-CLDN6 Reference Antibody (AB3-7)is more than 98.56%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-3-od450.jpgAnti-CLDN6 Reference Antibody (AB3-7)Immobilized human CLDN6 VLP Protein at 2 &mug/mL can bind Anti-CLDN6 Reference Antibody (AB3-7) https://www.bosterbio.com/catalog/product/view/id/1289442026-03-10T04:39:37+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-10-sds-page.jpgAnti-CLDN6 Reference Antibody (IMAB027)Anti-CLDN6 Reference Antibody (IMAB027) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-10-sec-hplc.jpgAnti-CLDN6 Reference Antibody (IMAB027)The purity of Anti-CLDN6 Reference Antibody (IMAB027)is more than 98.41%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-10-od450.jpgAnti-CLDN6 Reference Antibody (IMAB027)Immobilized human CLDN6 VLP at 8 &mug/mL can bind Anti-CLDN6 Reference Antibody (IMAB027)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-10-facs.jpgAnti-CLDN6 Reference Antibody (IMAB027)Human CLDN6 CHO cells were stained with Anti-CLDN6 Reference Antibody (IMAB027) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-10-luminescence-intensity.jpgAnti-CLDN6 Reference Antibody (IMAB027)Anti-CLDN6 Reference Antibody (IMAB027)-induced ADCC activity was evaluated using Human CD16a (158V) (Luc) Jurkat Reporter Cell. The max induction fold was approximately 14.16https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-10-internalizaton-rate.jpgAnti-CLDN6 Reference Antibody (IMAB027)Anti-CLDN6 Reference Antibody (IMAB027) by huCLDN6-HEK293 increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-10-xenograft-cldn6-ov90-cell-model.jpgAnti-CLDN6 Reference Antibody (IMAB027)IMAB027 inhibited the tumor growth of OV90 on Balb/c nude mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1289452026-03-10T04:39:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-5-sds-page.jpgAnti-CLDN6 Reference Antibody (64A)Anti-CLDN6 Reference Antibody (64A) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-5-sec-hplc.jpgAnti-CLDN6 Reference Antibody (64A)The purity of Anti-CLDN6 Reference Antibody (64A)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289462026-03-10T04:39:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-6-sds-page.jpgAnti-CLDN6 Reference Antibody (AB1-11)Anti-CLDN6 Reference Antibody (AB1-11) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-6-sec-hplc.jpgAnti-CLDN6 Reference Antibody (AB1-11)The purity of Anti-CLDN6 Reference Antibody (AB1-11)is more than 98.29% https://www.bosterbio.com/catalog/product/view/id/1289472026-03-10T04:39:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-7-sds-page.jpgAnti-CLDN6 Reference Antibody (AE3-20)Anti-CLDN6 Reference Antibody (AE3-20) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-7-sec-hplc.jpgAnti-CLDN6 Reference Antibody (AE3-20)The purity of Anti-CLDN6 Reference Antibody (AE3-20)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289482026-03-10T04:39:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-8-sds-page.jpgAnti-CLDN6 Reference Antibody (IM-301)Anti-CLDN6 Reference Antibody (IM-301) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-8-sec-hplc.jpgAnti-CLDN6 Reference Antibody (IM-301)The purity of Anti-CLDN6 Reference Antibody (IM-301)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289492026-03-10T04:39:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-9-sds-page.jpgAnti-CLDN6 Reference Antibody (IM-302)Anti-CLDN6 Reference Antibody (IM-302) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-9-sec-hplc.jpgAnti-CLDN6 Reference Antibody (IM-302)The purity of Anti-CLDN6 Reference Antibody (IM-302)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289502026-03-10T04:39:38+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-4-sds-page.jpgAnti-CLDN6 Reference Antibody (DS-9606a)Anti-CLDN6 Reference Antibody (DS-9606a) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-4-sec-hplc.jpgAnti-CLDN6 Reference Antibody (DS-9606a)The purity of Anti-CLDN6 Reference Antibody (DS-9606a)is more than 99.37%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-4-od450.jpgAnti-CLDN6 Reference Antibody (DS-9606a)Immobilized human CLDN6 VLP Protein at 2 &mug/mL can bind Anti-CLDN6 Reference Antibody (DS-9606a)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-4-facs.jpgAnti-CLDN6 Reference Antibody (DS-9606a)Human CLDN6 CHO cells were stained with Anti-CLDN6 Reference Antibody (DS-9606a) and negative control protein respectivelyhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-4-inhibition-of-cell-growth.jpgAnti-CLDN6 Reference Antibody (DS-9606a)DS-9606a by huCLDN6-HEK293 increased with the increase of antibody concentrationhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08182-4-xenograft-pa-1-cell-model.jpgAnti-CLDN6 Reference Antibody (DS-9606a)DS-9606a inhibited the tumor growth of PA-1 on Balb/c nude mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1289512026-03-10T04:39:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08183-1-sds-page.jpgAnti-LY75 / CD205/DEC-205 Reference Antibody (MEN1309)Anti-LY75/CD205/DEC-205 Reference Antibody (MEN1309) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08183-1-sec-hplc.jpgAnti-LY75 / CD205/DEC-205 Reference Antibody (MEN1309)The purity of Anti-LY75/CD205/DEC-205 Reference Antibody (MEN1309)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289522026-03-10T04:39:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08183-2-sds-page.jpgAnti-LY75 / CD205/DEC-205 Reference Antibody (CDX-1401)Anti-LY75/CD205/DEC-205 Reference Antibody (CDX-1401) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08183-2-sec-hplc.jpgAnti-LY75 / CD205/DEC-205 Reference Antibody (CDX-1401)The purity of Anti-LY75/CD205/DEC-205 Reference Antibody (CDX-1401)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289532026-03-10T04:39:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08199-1-sds-page.jpgAnti-LRRC32 / TGFbeta1 Reference Antibody (Livmoniplimab) Anti-LRRC32/TGFbeta1 Reference Antibody (Livmoniplimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08199-1-sec-hplc.jpgAnti-LRRC32 / TGFbeta1 Reference Antibody (Livmoniplimab) The purity of Anti-LRRC32/TGFbeta1 Reference Antibody (Livmoniplimab) is more than 99.25% https://www.bosterbio.com/catalog/product/view/id/1289542026-03-10T04:39:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08209-sds-page.jpgAnti-CD11 Reference Antibody (Rovelizumab)Anti-CD11 Reference Antibody (Rovelizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08209-sec-hplc.jpgAnti-CD11 Reference Antibody (Rovelizumab)The purity of Anti-CD11 Reference Antibody (Rovelizumab)is more than 99.22% https://www.bosterbio.com/catalog/product/view/id/1289552026-03-10T04:39:39+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1289562026-03-10T04:39:39+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08798-sds-page.jpgAnti-TEM7R / PLXDC2 Reference Antibody (Fox Chase patent anti-TEM7R)Anti-TEM7R/PLXDC2 Reference Antibody (Fox Chase patent anti-TEM7R) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08798-sec-hplc.jpgAnti-TEM7R / PLXDC2 Reference Antibody (Fox Chase patent anti-TEM7R)The purity of Anti-TEM7R/PLXDC2 Reference Antibody (Fox Chase patent anti-TEM7R)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289572026-03-10T04:39:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09006-sds-page.jpgAnti-SLITRK6 Reference Antibody (sirtratumab)Anti-SLITRK6 Reference Antibody (sirtratumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09006-sec-hplc.jpgAnti-SLITRK6 Reference Antibody (sirtratumab)The purity of Anti-SLITRK6 Reference Antibody (sirtratumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09006-od450.jpgAnti-SLITRK6 Reference Antibody (sirtratumab)Immobilized human SLITRK6 His at 2 &mug/mL can bind Anti-SLITRK6 Reference Antibody (sirtratumab) https://www.bosterbio.com/catalog/product/view/id/1289582026-03-10T04:39:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09006-1-sds-page.jpgAnti-SLITRK6 Reference Antibody (Sirtratumab vedotin)Anti-SLITRK6 Reference Antibody (Sirtratumab vedotin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09006-1-sec-hplc.jpgAnti-SLITRK6 Reference Antibody (Sirtratumab vedotin)The purity of Anti-SLITRK6 Reference Antibody (Sirtratumab vedotin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289592026-03-10T04:39:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09129-1-sds-page.jpgAnti-CLDN18.2 Reference Antibody (zolbetuximab)Anti-CLDN18.2 Reference Antibody (zolbetuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09129-1-sec-hplc.jpgAnti-CLDN18.2 Reference Antibody (zolbetuximab)The purity of Anti-CLDN18.2 Reference Antibody (zolbetuximab)is more than 96.05%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09129-1-od450.jpgAnti-CLDN18.2 Reference Antibody (zolbetuximab)Immobilized human CLDN18.2 VLP at 2 &mug/mL can bind Anti-CLDN18.2 Reference Antibody (zolbetuximab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09129-1-syngenic-mc38-18.2-cell-model.jpgAnti-CLDN18.2 Reference Antibody (zolbetuximab)Zolbetuximab inhibited the tumor growth of CLDN18.2-MC38 (Mouse colorectal cancer cells) on C57BL/6N mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1289602026-03-10T04:39:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09153-sds-page.jpgAnti-Siglec-8 Reference Antibody (lirentelimab)Anti-Siglec-8 Reference Antibody (lirentelimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09153-sec-hplc.jpgAnti-Siglec-8 Reference Antibody (lirentelimab)The purity of Anti-Siglec-8 Reference Antibody (lirentelimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289612026-03-10T04:39:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-sds-page.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (batoclimab)Anti-FcRn (FCGRT & B2M) Reference Antibody (batoclimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-sec-hplc.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (batoclimab)The purity of Anti-FcRn (FCGRT & B2M) Reference Antibody (batoclimab)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-od450.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (batoclimab)Immobilized human b2M L FCRn at 2 &mug/mL can bind Anti-FcRn (FCGRT & B2M) Reference Antibody (batoclimab) https://www.bosterbio.com/catalog/product/view/id/1289622026-03-10T04:39:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-1-sds-page.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (nipocalimab)Anti-FcRn (FCGRT & B2M) Reference Antibody (nipocalimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-1-sec-hplc.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (nipocalimab)The purity of Anti-FcRn (FCGRT & B2M) Reference Antibody (nipocalimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-1-od450.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (nipocalimab)Immobilized human FcRn/FCGRT&B2M Heterodimer protein https://www.bosterbio.com/catalog/product/view/id/1289632026-03-10T04:39:40+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-2-sds-page.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (rozanolixizumab)Anti-FcRn (FCGRT & B2M) Reference Antibody (rozanolixizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-2-sec-hplc.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (rozanolixizumab)The purity of Anti-FcRn (FCGRT & B2M) Reference Antibody (rozanolixizumab)is more than 97.55%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-2-od450.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (rozanolixizumab)Immobilized FcRn(FCGRT) His+FcRn(B2M) at 2 &mug/mL can bind Anti-FcRn (FCGRT & B2M) Reference Antibody (rozanolixizumab) https://www.bosterbio.com/catalog/product/view/id/1289642026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-3-sds-page.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (orilanolimab)Anti-FcRn (FCGRT & B2M) Reference Antibody (orilanolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-3-sec-hplc.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (orilanolimab)The purity of Anti-FcRn (FCGRT & B2M) Reference Antibody (orilanolimab)is more than 92.74%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09198-3-od450.jpgAnti-FcRn (FCGRT & B2M) Reference Antibody (orilanolimab)Immobilized FcRn(FCGRT) His+FcRn(B2M) at 2 &mug/mL can bind Anti-FcRn (FCGRT & B2M) Reference Antibody (orilanolimab) https://www.bosterbio.com/catalog/product/view/id/1289652026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09203-1-sds-page.jpgAnti-IL-1RL2 / IL-36R Reference Antibody (spesolimab)Anti-IL-1RL2/IL-36R Reference Antibody (spesolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09203-1-sec-hplc.jpgAnti-IL-1RL2 / IL-36R Reference Antibody (spesolimab)The purity of Anti-IL-1RL2/IL-36R Reference Antibody (spesolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289662026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09203-2-sds-page.jpgAnti-IL-1RL2 / IL-36R Reference Antibody (imsidolimab)Anti-IL-1RL2/IL-36R Reference Antibody (imsidolimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09203-2-sec-hplc.jpgAnti-IL-1RL2 / IL-36R Reference Antibody (imsidolimab)The purity of Anti-IL-1RL2/IL-36R Reference Antibody (imsidolimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289672026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09230-sds-page.jpgAnti-EFNA4 Reference Antibody (PF-06647263)Anti-EFNA4 Reference Antibody (PF-06647263) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09230-sec-hplc.jpgAnti-EFNA4 Reference Antibody (PF-06647263)The purity of Anti-EFNA4 Reference Antibody (PF-06647263)is more than 99.22% https://www.bosterbio.com/catalog/product/view/id/1289682026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09351-sds-page.jpgAnti-HGFA Reference Antibody (Genentech patent anti-HGFA )Anti-HGFA Reference Antibody (Genentech patent anti-HGFA ) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09351-sec-hplc.jpgAnti-HGFA Reference Antibody (Genentech patent anti-HGFA )The purity of Anti-HGFA Reference Antibody (Genentech patent anti-HGFA )is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289692026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09496-sds-page.jpgAnti-Ly6E Reference Antibody (RG7841)Anti-Ly6E Reference Antibody (RG7841) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09496-sec-hplc.jpgAnti-Ly6E Reference Antibody (RG7841)The purity of Anti-Ly6E Reference Antibody (RG7841)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289702026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-sds-page.jpgAnti-IFNa1 Reference Antibody (sifalimumab)Anti-IFNa1 Reference Antibody (sifalimumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-sec-hplc.jpgAnti-IFNa1 Reference Antibody (sifalimumab)The purity of Anti-IFNa1 Reference Antibody (sifalimumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-od450.jpgAnti-IFNa1 Reference Antibody (sifalimumab)Immobilized human IFNa1 https://www.bosterbio.com/catalog/product/view/id/1289712026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-1-sds-page.jpgAnti-IFNa1 Reference Antibody (rontalizumab)Anti-IFNa1 Reference Antibody (rontalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-1-sec-hplc.jpgAnti-IFNa1 Reference Antibody (rontalizumab)The purity of Anti-IFNa1 Reference Antibody (rontalizumab)is more than 94.51% https://www.bosterbio.com/catalog/product/view/id/1289722026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-2-sds-page.jpgAnti-IFNa1 Reference Antibody (Baylor patent anti-IFN alpha)Anti-IFNa1 Reference Antibody (Baylor patent anti-IFN alpha) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-2-sec-hplc.jpgAnti-IFNa1 Reference Antibody (Baylor patent anti-IFN alpha)The purity of Anti-IFNa1 Reference Antibody (Baylor patent anti-IFN alpha)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289732026-03-10T04:39:41+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-3-sds-page.jpgAnti-IFNa1 Reference Antibody (Chinese CDC patent anti-Interferon Alpha)Anti-IFNa1 Reference Antibody (Chinese CDC patent anti-Interferon Alpha) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09608-3-sec-hplc.jpgAnti-IFNa1 Reference Antibody (Chinese CDC patent anti-Interferon Alpha)The purity of Anti-IFNa1 Reference Antibody (Chinese CDC patent anti-Interferon Alpha)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289742026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09611-sds-page.jpgAnti-LILRA4 / ILT7 / CD85g Reference Antibody (daxdilimab)Anti-LILRA4/ILT7/CD85g Reference Antibody (daxdilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09611-sec-hplc.jpgAnti-LILRA4 / ILT7 / CD85g Reference Antibody (daxdilimab)The purity of Anti-LILRA4/ILT7/CD85g Reference Antibody (daxdilimab)is more than 96.58%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09611-od450.jpgAnti-LILRA4 / ILT7 / CD85g Reference Antibody (daxdilimab)Immobilized human ILT7 His at 2 &mug/mL can bind Anti-LILRA4/ILT7/CD85g Reference Antibody (daxdilimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09611-facs.jpgAnti-LILRA4 / ILT7 / CD85g Reference Antibody (daxdilimab)Human ILT7 HEK293 cells were stained with Anti-LILRA4/ILT7/CD85g Reference Antibody (daxdilimab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1289752026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09624-sds-page.jpgAnti-PTGFRN / CD315 Reference Antibody (AG02-ADC)Anti-PTGFRN/CD315 Reference Antibody (AG02-ADC) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09624-sec-hplc.jpgAnti-PTGFRN / CD315 Reference Antibody (AG02-ADC)The purity of Anti-PTGFRN/CD315 Reference Antibody (AG02-ADC)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289762026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09747-sds-page.jpgAnti-B7-H6 / NCR3LG1 Reference Antibody (Dartmouth patent anti-B7-H6)Anti-B7-H6/NCR3LG1 Reference Antibody (Dartmouth patent anti-B7-H6) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09747-sec-hplc.jpgAnti-B7-H6 / NCR3LG1 Reference Antibody (Dartmouth patent anti-B7-H6)The purity of Anti-B7-H6/NCR3LG1 Reference Antibody (Dartmouth patent anti-B7-H6)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289772026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09768-sds-page.jpgAnti-DCBLD2 / ESDN Reference Antibody (FA19-1)Anti-DCBLD2/ESDN Reference Antibody (FA19-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09768-sec-hplc.jpgAnti-DCBLD2 / ESDN Reference Antibody (FA19-1)The purity of Anti-DCBLD2/ESDN Reference Antibody (FA19-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289782026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09811-sds-page.jpgAnti-SEZ6 Reference Antibody (Abbv-011)Anti-SEZ6 Reference Antibody (Abbv-011) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09811-sec-hplc.jpgAnti-SEZ6 Reference Antibody (Abbv-011)The purity of Anti-SEZ6 Reference Antibody (Abbv-011)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289792026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09859-1-sds-page.jpgAnti-IL-20Ra Reference Antibody (Cheng Kung U. patent anti-IL-20R1)Anti-IL-20Ra Reference Antibody (Cheng Kung U. patent anti-IL-20R1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09859-1-sec-hplc.jpgAnti-IL-20Ra Reference Antibody (Cheng Kung U. patent anti-IL-20R1)The purity of Anti-IL-20Ra Reference Antibody (Cheng Kung U. patent anti-IL-20R1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289802026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09914-sds-page.jpgAnti-Clusterin Reference Antibody (AB-16B5)Anti-Clusterin Reference Antibody (AB-16B5) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m09914-sec-hplc.jpgAnti-Clusterin Reference Antibody (AB-16B5)The purity of Anti-Clusterin Reference Antibody (AB-16B5)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289812026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10180-sds-page.jpgAnti-Phosphorylcholine Reference Antibody (ATH3G10)Anti-Phosphorylcholine Reference Antibody (ATH3G10) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10180-sec-hplc.jpgAnti-Phosphorylcholine Reference Antibody (ATH3G10)The purity of Anti-Phosphorylcholine Reference Antibody (ATH3G10)is more than 96.73 % https://www.bosterbio.com/catalog/product/view/id/1289822026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10268-sds-page.jpgAnti-TMEFF1 / Tomoregulin-1 Reference Antibody (Bluefin patent anti-TMEFF1)Anti-TMEFF1/Tomoregulin-1 Reference Antibody (Bluefin patent anti-TMEFF1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10268-sec-hplc.jpgAnti-TMEFF1 / Tomoregulin-1 Reference Antibody (Bluefin patent anti-TMEFF1)The purity of Anti-TMEFF1/Tomoregulin-1 Reference Antibody (Bluefin patent anti-TMEFF1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289832026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10351-sds-page.jpgAnti-SIRPg / CD172g Reference Antibody (KWAR23)Anti-SIRPg/CD172g Reference Antibody (KWAR23) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10351-sec-hplc.jpgAnti-SIRPg / CD172g Reference Antibody (KWAR23)The purity of Anti-SIRPg/CD172g Reference Antibody (KWAR23)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10351-od450.jpgAnti-SIRPg / CD172g Reference Antibody (KWAR23)Immobilized human ALCAM His at 2 &mug/mL can bind Anti-SIRPg/CD172g Reference Antibody (KWAR23) https://www.bosterbio.com/catalog/product/view/id/1289842026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10368-sds-page.jpgAnti-TM4SF1 Reference Antibody (Beth Israel Patent Anti-TM4SF1)Anti-TM4SF1 Reference Antibody (Beth Israel Patent Anti-TM4SF1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10368-sec-hplc.jpgAnti-TM4SF1 Reference Antibody (Beth Israel Patent Anti-TM4SF1)The purity of Anti-TM4SF1 Reference Antibody (Beth Israel Patent Anti-TM4SF1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289852026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10986-sds-page.jpgAnti-GPR73 / PROKR1 Reference Antibody (Multiple seq-one in animal)Anti-GPR73/PROKR1 Reference Antibody (Multiple seq-one in animal) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m10986-sec-hplc.jpgAnti-GPR73 / PROKR1 Reference Antibody (Multiple seq-one in animal)The purity of Anti-GPR73/PROKR1 Reference Antibody (Multiple seq-one in animal)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289862026-03-10T04:39:42+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-2-sds-page.jpgAnti-BTN1A1 Reference Antibody (ICT-01)Anti-BTN1A1 Reference Antibody (ICT-01) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-2-sec-hplc.jpgAnti-BTN1A1 Reference Antibody (ICT-01)The purity of Anti-BTN1A1 Reference Antibody (ICT-01)is more than 98.38%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-2-od450.jpgAnti-BTN1A1 Reference Antibody (ICT-01)Immobilized human PVRIG His at 2 &mug/mL can bind Anti-BTN1A1 Reference Antibody (ICT-01)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-2-facs.jpgAnti-BTN1A1 Reference Antibody (ICT-01)Human BTN3 HEK293 cells were stained with Anti-BTN1A1 Reference Antibody (ICT-01) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1289872026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-3-sds-page.jpgAnti-BTN1A1 Reference Antibody (CTX-2026)Anti-BTN1A1 Reference Antibody (CTX-2026) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-3-sec-hplc.jpgAnti-BTN1A1 Reference Antibody (CTX-2026)The purity of Anti-BTN1A1 Reference Antibody (CTX-2026)is more than 98.77%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-3-od450.jpgAnti-BTN1A1 Reference Antibody (CTX-2026)Immobilized human PVRIG His at 2 &mug/mL can bind Anti-BTN1A1 Reference Antibody (CTX-2026)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-3-facs.jpgAnti-BTN1A1 Reference Antibody (CTX-2026)Human BTN3 HEK293 cells were stained with Anti-BTN1A1 Reference Antibody (CTX-2026) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1289882026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-4-sds-page.jpgAnti-BTN1A1 Reference Antibody (ICT-01-N297A)Anti-BTN1A1 Reference Antibody (ICT-01-N297A) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11266-4-sec-hplc.jpgAnti-BTN1A1 Reference Antibody (ICT-01-N297A)The purity of Anti-BTN1A1 Reference Antibody (ICT-01-N297A)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289892026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11590-sds-page.jpgAnti-LRRC15 / LIB Reference Antibody (samrotamab)Anti-LRRC15/LIB Reference Antibody (samrotamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11590-sec-hplc.jpgAnti-LRRC15 / LIB Reference Antibody (samrotamab)The purity of Anti-LRRC15/LIB Reference Antibody (samrotamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289902026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11640-sds-page.jpgAnti-CB1 / CNR1 Reference Antibody (nimacimab)Anti-CB1/CNR1 Reference Antibody (nimacimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11640-sec-hplc.jpgAnti-CB1 / CNR1 Reference Antibody (nimacimab)The purity of Anti-CB1/CNR1 Reference Antibody (nimacimab)is more than 99.42% https://www.bosterbio.com/catalog/product/view/id/1289912026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11640-1-sds-page.jpgAnti-CB1 / CNR1 Reference Antibody (GFB-024)Anti-CB1/CNR1 Reference Antibody (GFB-024) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11640-1-sec-hplc.jpgAnti-CB1 / CNR1 Reference Antibody (GFB-024)The purity of Anti-CB1/CNR1 Reference Antibody (GFB-024)is more than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m11640-1-facs.jpgAnti-CB1 / CNR1 Reference Antibody (GFB-024)Human CB1 EGFP CHOS cells were stained with Anti-CB1/CNR1 Reference Antibody (GFB-024) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1289922026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12456-sds-page.jpgAnti-Histone H1 Reference Antibody (derlotuximab)Anti-Histone H1 Reference Antibody (derlotuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12456-sec-hplc.jpgAnti-Histone H1 Reference Antibody (derlotuximab)The purity of Anti-Histone H1 Reference Antibody (derlotuximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289932026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-26-sds-page.jpgAnti-Histone H3 Reference Antibody (Immunomedics patent anti-Histone H3)Anti-Histone H3 Reference Antibody (Immunomedics patent anti-Histone H3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12477-26-sec-hplc.jpgAnti-Histone H3 Reference Antibody (Immunomedics patent anti-Histone H3)The purity of Anti-Histone H3 Reference Antibody (Immunomedics patent anti-Histone H3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289942026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12642-sds-page.jpgAnti-CLEC14A Reference Antibody (Scripps Korea patent anti-CLEC14A)Anti-CLEC14A Reference Antibody (Scripps Korea patent anti-CLEC14A) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12642-sec-hplc.jpgAnti-CLEC14A Reference Antibody (Scripps Korea patent anti-CLEC14A)The purity of Anti-CLEC14A Reference Antibody (Scripps Korea patent anti-CLEC14A)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289952026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12856-sds-page.jpgAnti-GPR44 / PTGDR2 / CD294 Reference Antibody (KHK patent anti-CRTH2)Anti-GPR44/PTGDR2/CD294 Reference Antibody (KHK patent anti-CRTH2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12856-sec-hplc.jpgAnti-GPR44 / PTGDR2 / CD294 Reference Antibody (KHK patent anti-CRTH2)The purity of Anti-GPR44/PTGDR2/CD294 Reference Antibody (KHK patent anti-CRTH2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289962026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12988-sds-page.jpgAnti-Melanotransferrin / CD228 Reference Antibody (SC-005)Anti-Melanotransferrin/CD228 Reference Antibody (SC-005) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m12988-sec-hplc.jpgAnti-Melanotransferrin / CD228 Reference Antibody (SC-005)The purity of Anti-Melanotransferrin/CD228 Reference Antibody (SC-005)is more than 99.21% https://www.bosterbio.com/catalog/product/view/id/1289972026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13075-sds-page.jpgAnti-GPC2 / Glypican 2 Reference Antibody (Nih Patent Anti-Glypican-2)Anti-GPC2/Glypican 2 Reference Antibody (Nih Patent Anti-Glypican-2) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13075-sec-hplc.jpgAnti-GPC2 / Glypican 2 Reference Antibody (Nih Patent Anti-Glypican-2)The purity of Anti-GPC2/Glypican 2 Reference Antibody (Nih Patent Anti-Glypican-2)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289982026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13374-sds-page.jpgAnti-KID3 Reference Antibody (Macrogenics patent anti-KID3)Anti-KID3 Reference Antibody (Macrogenics patent anti-KID3) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13374-sec-hplc.jpgAnti-KID3 Reference Antibody (Macrogenics patent anti-KID3)The purity of Anti-KID3 Reference Antibody (Macrogenics patent anti-KID3)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1289992026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13912-sds-page.jpgAnti-GPRC5D Reference Antibody (talquetamab)Anti-GPRC5D Reference Antibody (talquetamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13912-sec-hplc.jpgAnti-GPRC5D Reference Antibody (talquetamab)The purity of Anti-GPRC5D Reference Antibody (talquetamab)is more than 95.4%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13912-od450.jpgAnti-GPRC5D Reference Antibody (talquetamab)Immobilized human CD3E/CD3 epsilon Proteinhttps://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13912-facs.jpgAnti-GPRC5D Reference Antibody (talquetamab)Human GPRC5D HEK293 cells were stained with Anti-GPRC5D Reference Antibody (talquetamab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1290002026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14205-sds-page.jpgAnti-GPR20 Reference Antibody (DS-6157)Anti-GPR20 Reference Antibody (DS-6157) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14205-sec-hplc.jpgAnti-GPR20 Reference Antibody (DS-6157)The purity of Anti-GPR20 Reference Antibody (DS-6157)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290012026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14323-sds-page.jpgAnti-Siglec-15 / CD33L3 Reference Antibody (AB-25E9)Anti-Siglec-15/CD33L3 Reference Antibody (AB-25E9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14323-sec-hplc.jpgAnti-Siglec-15 / CD33L3 Reference Antibody (AB-25E9)The purity of Anti-Siglec-15/CD33L3 Reference Antibody (AB-25E9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290022026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14323-1-sds-page.jpgAnti-Siglec-15 / CD33L3 Reference Antibody (NC318)Anti-Siglec-15/CD33L3 Reference Antibody (NC318) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14323-1-sec-hplc.jpgAnti-Siglec-15 / CD33L3 Reference Antibody (NC318)The purity of Anti-Siglec-15/CD33L3 Reference Antibody (NC318)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1290032026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14323-2-sds-page.jpgAnti-Siglec-15 / CD33L3 Reference Antibody (Medimmune patent anti-Siglec-15)Anti-Siglec-15/CD33L3 Reference Antibody (Medimmune patent anti-Siglec-15) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14323-2-sec-hplc.jpgAnti-Siglec-15 / CD33L3 Reference Antibody (Medimmune patent anti-Siglec-15)The purity of Anti-Siglec-15/CD33L3 Reference Antibody (Medimmune patent anti-Siglec-15)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290042026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14402-sds-page.jpgAnti-DPEP3 Reference Antibody (tamrintamab)Anti-DPEP3 Reference Antibody (tamrintamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14402-sec-hplc.jpgAnti-DPEP3 Reference Antibody (tamrintamab)The purity of Anti-DPEP3 Reference Antibody (tamrintamab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290052026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-14-sds-page.jpgAnti-Histone H4 Reference Antibody (Immunomedics patent anti-Histone H4)Anti-Histone H4 Reference Antibody (Immunomedics patent anti-Histone H4) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m14495-14-sec-hplc.jpgAnti-Histone H4 Reference Antibody (Immunomedics patent anti-Histone H4)The purity of Anti-Histone H4 Reference Antibody (Immunomedics patent anti-Histone H4)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290062026-03-10T04:39:43+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m15623-sds-page.jpgAnti-ILDR2 Reference Antibody (bapotulimab)Anti-ILDR2 Reference Antibody (bapotulimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m15623-sec-hplc.jpgAnti-ILDR2 Reference Antibody (bapotulimab)The purity of Anti-ILDR2 Reference Antibody (bapotulimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290072026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m18603-sds-page.jpgAnti-PVRIG Reference Antibody (COM701)Anti-PVRIG Reference Antibody (COM701) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m18603-sec-hplc.jpgAnti-PVRIG Reference Antibody (COM701)The purity of Anti-PVRIG Reference Antibody (COM701)is more than 99.44%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m18603-od450.jpgAnti-PVRIG Reference Antibody (COM701)Immobilized human PVRIG His at 2 &mug/mL can bind Anti-PVRIG Reference Antibody (COM701) https://www.bosterbio.com/catalog/product/view/id/1290092026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m18624-sds-page.jpgAnti-KAAG1 Reference Antibody (ADCT-901)Anti-KAAG1 Reference Antibody (ADCT-901) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m18624-sec-hplc.jpgAnti-KAAG1 Reference Antibody (ADCT-901)The purity of Anti-KAAG1 Reference Antibody (ADCT-901)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290102026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m18624-1-sds-page.jpgAnti-KAAG1 Reference Antibody (ADCT-901-MMAE)Anti-KAAG1 Reference Antibody (ADCT-901-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m18624-1-sec-hplc.jpgAnti-KAAG1 Reference Antibody (ADCT-901-MMAE)The purity of Anti-KAAG1 Reference Antibody (ADCT-901-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290112026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/2/m29279-sds-page.jpgAnti-CCN2 / CTGF Reference Antibody (pamrevlumab)Anti-CCN2/CTGF Reference Antibody (pamrevlumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/2/m29279-sec-hplc.jpgAnti-CCN2 / CTGF Reference Antibody (pamrevlumab)The purity of Anti-CCN2/CTGF Reference Antibody (pamrevlumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/2/m29279-od450.jpgAnti-CCN2 / CTGF Reference Antibody (pamrevlumab)Immobilized human CTGF His at 2 &mug/mL can bind Anti-CCN2/CTGF Reference Antibody (pamrevlumab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/2/m29279-xenograft-colo205-cell-model.jpgAnti-CCN2 / CTGF Reference Antibody (pamrevlumab)Pamrevlumab inhibited the tumor growth of COLO205 on Balb/c nude mice. The result showed significant anti-tumor effects https://www.bosterbio.com/catalog/product/view/id/1290122026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30935-sds-page.jpgAnti-PA Reference Antibody (Raxibacumab)Anti-PA Reference Antibody (Raxibacumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30935-sec-hplc.jpgAnti-PA Reference Antibody (Raxibacumab)The purity of Anti-PA Reference Antibody (Raxibacumab)is more than 98.88% https://www.bosterbio.com/catalog/product/view/id/1290132026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31965-sds-page.jpgAnti-P-Selectin / CD62p Reference Antibody (crizanlizumab)Anti-P-Selectin/CD62p Reference Antibody (crizanlizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m31965-sec-hplc.jpgAnti-P-Selectin / CD62p Reference Antibody (crizanlizumab)The purity of Anti-P-Selectin/CD62p Reference Antibody (crizanlizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290142026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m32104-1-sds-page.jpgAnti-RGMC / HFE2 Reference Antibody (DISC-0974)Anti-RGMC/HFE2 Reference Antibody (DISC-0974) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m32104-1-sec-hplc.jpgAnti-RGMC / HFE2 Reference Antibody (DISC-0974)The purity of Anti-RGMC/HFE2 Reference Antibody (DISC-0974)is more than 98.22 % https://www.bosterbio.com/catalog/product/view/id/1290152026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m32320-1-sds-page.jpgAnti-B7-H5 / VISTA Reference Antibody (onvatilimab)Anti-B7-H5/VISTA Reference Antibody (onvatilimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m32320-1-sec-hplc.jpgAnti-B7-H5 / VISTA Reference Antibody (onvatilimab)The purity of Anti-B7-H5/VISTA Reference Antibody (onvatilimab)is more than 98.11%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m32320-1-od450.jpgAnti-B7-H5 / VISTA Reference Antibody (onvatilimab)Immobilized human B7-H5/VISTA His at 2 &mug/mL can bind Anti-B7-H5/VISTA Reference Antibody (onvatilimab)https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m32320-1-facs.jpgAnti-B7-H5 / VISTA Reference Antibody (onvatilimab)Human B7H5 CHO-K cells were stained with Anti-B7-H5/VISTA Reference Antibody (onvatilimab) and negative control protein respectively https://www.bosterbio.com/catalog/product/view/id/1290162026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-sds-page.jpgAnti-Spike RBD Reference Antibody (Sotrovimab)Anti-Spike RBD Reference Antibody (Sotrovimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Sotrovimab)The purity of Anti-Spike RBD Reference Antibody (Sotrovimab)is more than 96.6%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-od450.jpgAnti-Spike RBD Reference Antibody (Sotrovimab)Immobilized 2019nCoV RBD His at 2 &mug/mL can bind Anti-Spike RBD Reference Antibody (Sotrovimab) https://www.bosterbio.com/catalog/product/view/id/1290172026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-1-sds-page.jpgAnti-Spike RBD Reference Antibody (Imdevimab)Anti-Spike RBD Reference Antibody (Imdevimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-1-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Imdevimab)The purity of Anti-Spike RBD Reference Antibody (Imdevimab)is more than 99.54%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-1-od450.jpgAnti-Spike RBD Reference Antibody (Imdevimab)Immobilized 2019nCoV RBD His at 2 &mug/mL can bind Anti-Spike RBD Reference Antibody (Imdevimab) https://www.bosterbio.com/catalog/product/view/id/1290182026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-2-sds-page.jpgAnti-Spike RBD Reference Antibody (Etesevimab)Anti-Spike RBD Reference Antibody (Etesevimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-2-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Etesevimab)The purity of Anti-Spike RBD Reference Antibody (Etesevimab)is more than 98.76%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-2-od450.jpgAnti-Spike RBD Reference Antibody (Etesevimab)Immobilized 2019nCoV RBD His at 2 &mug/mL can bind Anti-Spike RBD Reference Antibody (Etesevimab) https://www.bosterbio.com/catalog/product/view/id/1290192026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-3-sds-page.jpgAnti-Spike RBD Reference Antibody (Regdanvimab)Anti-Spike RBD Reference Antibody (Regdanvimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-3-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Regdanvimab)The purity of Anti-Spike RBD Reference Antibody (Regdanvimab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-3-od450.jpgAnti-Spike RBD Reference Antibody (Regdanvimab)Immobilized 2019nCoV RBD His at 2 &mug/mL can bind Anti-Spike RBD Reference Antibody (Regdanvimab) https://www.bosterbio.com/catalog/product/view/id/1290202026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-4-sds-page.jpgAnti-Spike RBD Reference Antibody (Cilgavimab)Anti-Spike RBD Reference Antibody (Cilgavimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-4-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Cilgavimab)The purity of Anti-Spike RBD Reference Antibody (Cilgavimab)is more than 99.35%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-4-od450.jpgAnti-Spike RBD Reference Antibody (Cilgavimab)Immobilized 2019nCoV RBD His at 2 &mug/mL can bind Anti-Spike RBD Reference Antibody (Cilgavimab) https://www.bosterbio.com/catalog/product/view/id/1290212026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-5-sds-page.jpgAnti-Spike RBD Reference Antibody (Casirivimab)Anti-Spike RBD Reference Antibody (Casirivimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-5-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Casirivimab)The purity of Anti-Spike RBD Reference Antibody (Casirivimab)is more than 99.84%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-5-od450.jpgAnti-Spike RBD Reference Antibody (Casirivimab)Immobilized 2019nCoV RBD His at 2 &mug/mL can bind Anti-Spike RBD Reference Antibody (Casirivimab) https://www.bosterbio.com/catalog/product/view/id/1290222026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-sds-page.jpgAnti-IgE Reference Antibody (talizumab)Anti-IgE Reference Antibody (talizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-sec-hplc.jpgAnti-IgE Reference Antibody (talizumab)The purity of Anti-IgE Reference Antibody (talizumab)is more than 100%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-od450.jpgAnti-IgE Reference Antibody (talizumab)Immobilized human PD 1 His at 2 &mug/mL can bind Anti-IgE Reference Antibody (talizumab) https://www.bosterbio.com/catalog/product/view/id/1290232026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-3-sds-page.jpgAnti-Clathrin Heavy Chain / CHC Reference Antibody (Academia Sinica patent anti-Clathrin Heavy ChainAnti-Clathrin Heavy Chain/CHC Reference Antibody (Academia Sinica patent anti-Clathrin Heavy Chain) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m03134-3-sec-hplc.jpgAnti-Clathrin Heavy Chain / CHC Reference Antibody (Academia Sinica patent anti-Clathrin Heavy ChainThe purity of Anti-Clathrin Heavy Chain/CHC Reference Antibody (Academia Sinica patent anti-Clathrin Heavy Chain)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290242026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34014-sds-page.jpgAnti-FZD Reference Antibody (vantictumab)Anti-FZD Reference Antibody (vantictumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34014-sec-hplc.jpgAnti-FZD Reference Antibody (vantictumab)The purity of Anti-FZD Reference Antibody (vantictumab)is more than 98.99% https://www.bosterbio.com/catalog/product/view/id/1290252026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30379-2-sds-page.jpgAnti-HBsAg Reference Antibody (OST 577)Anti-HBsAg Reference Antibody (OST 577) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m30379-2-sec-hplc.jpgAnti-HBsAg Reference Antibody (OST 577)The purity of Anti-HBsAg Reference Antibody (OST 577)is more than 98.4% https://www.bosterbio.com/catalog/product/view/id/1290262026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34015-sds-page.jpgAnti-TCR Reference Antibody (TOL101)Anti-TCR Reference Antibody (TOL101) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34015-sec-hplc.jpgAnti-TCR Reference Antibody (TOL101)The purity of Anti-TCR Reference Antibody (TOL101)is more than 98.12% https://www.bosterbio.com/catalog/product/view/id/1290272026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-4-sds-page.jpgAnti-glycoprotein (GP) Iib / IIIa Reference Antibody (Abciximab) Anti-glycoprotein (GP) Iib/IIIa Reference Antibody (Abciximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m01102-4-sec-hplc.jpgAnti-glycoprotein (GP) Iib / IIIa Reference Antibody (Abciximab) The purity of Anti-glycoprotein (GP) Iib/IIIa Reference Antibody (Abciximab) is more than 99.7% https://www.bosterbio.com/catalog/product/view/id/1290282026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-1-sds-page.jpgAnti-RSV glycoprotein F Reference Antibody (Suptavumab)Anti-RSV glycoprotein F Reference Antibody (Suptavumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-1-sec-hplc.jpgAnti-RSV glycoprotein F Reference Antibody (Suptavumab)The purity of Anti-RSV glycoprotein F Reference Antibody (Suptavumab)is more than 98.77% https://www.bosterbio.com/catalog/product/view/id/1290292026-03-10T04:39:44+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34017-sds-page.jpgAnti-EBOV Reference Antibody (Atoltivimab)Anti-EBOV Reference Antibody (Atoltivimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34017-sec-hplc.jpgAnti-EBOV Reference Antibody (Atoltivimab)The purity of Anti-EBOV Reference Antibody (Atoltivimab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290302026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-2-sds-page.jpgAnti-RSV-F Reference Antibody (palivizumab)Anti-RSV-F Reference Antibody (palivizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-2-sec-hplc.jpgAnti-RSV-F Reference Antibody (palivizumab)The purity of Anti-RSV-F Reference Antibody (palivizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290312026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34018-sds-page.jpgAnti-SpA Reference Antibody (Omodenbamab)Anti-SpA Reference Antibody (Omodenbamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34018-sec-hplc.jpgAnti-SpA Reference Antibody (Omodenbamab)The purity of Anti-SpA Reference Antibody (Omodenbamab)is more than 96.8% https://www.bosterbio.com/catalog/product/view/id/1290322026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-sds-page.jpgAnti-RSV Reference Antibody (Nirsevimab)Anti-RSV Reference Antibody (Nirsevimabㄘ on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-sec-hplc.jpgAnti-RSV Reference Antibody (Nirsevimab)The purity of Anti-RSV Reference Antibody (Nirsevimabㄘis more than 95% https://www.bosterbio.com/catalog/product/view/id/1290332026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13556-sds-page.jpgAnti-GFRAL Reference Antibody (NGM120)Anti-GFRAL Reference Antibody (NGM120) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/1/m13556-sec-hplc.jpgAnti-GFRAL Reference Antibody (NGM120)The purity of Anti-GFRAL Reference Antibody (NGM120)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1290342026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34019-sds-page.jpgAnti-GD2 Reference Antibody (naxitamab)Anti-GD2 Reference Antibody (naxitamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34019-sec-hplc.jpgAnti-GD2 Reference Antibody (naxitamab)The purity of Anti-GD2 Reference Antibody (naxitamab)is more than 100.00 % https://www.bosterbio.com/catalog/product/view/id/1290352026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-3-sds-page.jpgAnti-RSV-F Reference Antibody (motavizumab)Anti-RSV-F Reference Antibody (motavizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34016-3-sec-hplc.jpgAnti-RSV-F Reference Antibody (motavizumab)The purity of Anti-RSV-F Reference Antibody (motavizumab)is more than 98.3% https://www.bosterbio.com/catalog/product/view/id/1290362026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-1-sds-page.jpgAnti-IgE Reference Antibody (omalizumab)Anti-IgE Reference Antibody (omalizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-1-sec-hplc.jpgAnti-IgE Reference Antibody (omalizumab)The purity of Anti-IgE Reference Antibody (omalizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290372026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34020-sds-page.jpgAnti-oxLDL Reference Antibody (orticumab)Anti-oxLDL Reference Antibody (orticumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34020-sec-hplc.jpgAnti-oxLDL Reference Antibody (orticumab)The purity of Anti-oxLDL Reference Antibody (orticumab)is more than 97.79% https://www.bosterbio.com/catalog/product/view/id/1290382026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34021-sds-page.jpgAnti-Lewis Y Reference Antibody (MB 311)Anti-Lewis Y Reference Antibody (MB 311) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34021-sec-hplc.jpgAnti-Lewis Y Reference Antibody (MB 311)The purity of Anti-Lewis Y Reference Antibody (MB 311)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290392026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08425-sds-page.jpgAnti-SARS-CoV-2 Reference Antibody (Bebtelovimab)Anti-SARS-CoV-2 Reference Antibody (Bebtelovimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08425-sec-hplc.jpgAnti-SARS-CoV-2 Reference Antibody (Bebtelovimab)The purity of Anti-SARS-CoV-2 Reference Antibody (Bebtelovimab)is more than 97% https://www.bosterbio.com/catalog/product/view/id/1290402026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-2-sds-page.jpgAnti-IgE Reference Antibody (ligelizumab)Anti-IgE Reference Antibody (ligelizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-2-sec-hplc.jpgAnti-IgE Reference Antibody (ligelizumab)The purity of Anti-IgE Reference Antibody (ligelizumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290412026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-sds-page.jpgAnti-Zaire Ebola virus Reference Antibody (Larcaviximab)Anti-Zaire Ebola virus Reference Antibody (Larcaviximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-sec-hplc.jpgAnti-Zaire Ebola virus Reference Antibody (Larcaviximab)The purity of Anti-Zaire Ebola virus Reference Antibody (Larcaviximab)is more than 96.13% https://www.bosterbio.com/catalog/product/view/id/1290422026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34023-sds-page.jpgAnti-GD3 Reference Antibody (ecromeximab)Anti-GD3 Reference Antibody (ecromeximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34023-sec-hplc.jpgAnti-GD3 Reference Antibody (ecromeximab)The purity of Anti-GD3 Reference Antibody (ecromeximab)is more than 96.37% https://www.bosterbio.com/catalog/product/view/id/1290432026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34024-sds-page.jpgAnti-CanAg Reference Antibody (Cantuzumab ravtansine)Anti-CanAg Reference Antibody (Cantuzumab ravtansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34024-sec-hplc.jpgAnti-CanAg Reference Antibody (Cantuzumab ravtansine)The purity of Anti-CanAg Reference Antibody (Cantuzumab ravtansine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290442026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34021-1-sds-page.jpgAnti-Sialyl-Lewis A Reference Antibody (MVT-5873)Anti-Sialyl-Lewis A Reference Antibody (MVT-5873) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34021-1-sec-hplc.jpgAnti-Sialyl-Lewis A Reference Antibody (MVT-5873)The purity of Anti-Sialyl-Lewis A Reference Antibody (MVT-5873)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1290452026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34024-1-sds-page.jpgAnti-CanAg Reference Antibody (Cantuzumab)Anti-CanAg Reference Antibody (Cantuzumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34024-1-sec-hplc.jpgAnti-CanAg Reference Antibody (Cantuzumab)The purity of Anti-CanAg Reference Antibody (Cantuzumab)is more than 100.00% https://www.bosterbio.com/catalog/product/view/id/1290462026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34025-sds-page.jpgAnti-MU5AC Reference Antibody (ensituximab)Anti-MU5AC Reference Antibody (ensituximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34025-sec-hplc.jpgAnti-MU5AC Reference Antibody (ensituximab)The purity of Anti-MU5AC Reference Antibody (ensituximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290472026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34026-sds-page.jpgAnti-Rabies virus GP Reference Antibody (foravirumab)Anti-Rabies virus GP Reference Antibody (foravirumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34026-sec-hplc.jpgAnti-Rabies virus GP Reference Antibody (foravirumab)The purity of Anti-Rabies virus GP Reference Antibody (foravirumab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1290482026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34019-1-sds-page.jpgAnti-GD2 Reference Antibody (dinutuximab)Anti-GD2 Reference Antibody (dinutuximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34019-1-sec-hplc.jpgAnti-GD2 Reference Antibody (dinutuximab)The purity of Anti-GD2 Reference Antibody (dinutuximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290492026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-6-sds-page.jpgAnti-Spike RBD Reference Antibody (Romlusevimab)Anti-Spike RBD Reference Antibody (Romlusevimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-6-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Romlusevimab)The purity of Anti-Spike RBD Reference Antibody (Romlusevimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1290502026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-7-sds-page.jpgAnti-Spike RBD Reference Antibody (Amubarvimab)Anti-Spike RBD Reference Antibody (Amubarvimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-7-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Amubarvimab)The purity of Anti-Spike RBD Reference Antibody (Amubarvimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1290512026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34027-sds-page.jpgAnti-PcrV Reference Antibody (Gremubamab)Anti-PcrV Reference Antibody (Gremubamab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34027-sec-hplc.jpgAnti-PcrV Reference Antibody (Gremubamab)The purity of Anti-PcrV Reference Antibody (Gremubamab)is more than 93.84% https://www.bosterbio.com/catalog/product/view/id/1290522026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34028-sds-page.jpgAnti-RG1 Reference Antibody (19G9)Anti-RG1 Reference Antibody (19G9) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34028-sec-hplc.jpgAnti-RG1 Reference Antibody (19G9)The purity of Anti-RG1 Reference Antibody (19G9)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290532026-03-10T04:39:45+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-8-sds-page.jpgAnti-Spike RBD Reference Antibody (Tixagevimab)Anti-Spike RBD Reference Antibody (Tixagevimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34012-8-sec-hplc.jpgAnti-Spike RBD Reference Antibody (Tixagevimab)The purity of Anti-Spike RBD Reference Antibody (Tixagevimab)is more than 100% https://www.bosterbio.com/catalog/product/view/id/1290542026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34029-sds-page.jpgAnti-alpha-toxin Reference Antibody (Suvratoxumab)Anti-alpha-toxin Reference Antibody (Suvratoxumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34029-sec-hplc.jpgAnti-alpha-toxin Reference Antibody (Suvratoxumab)The purity of Anti-alpha-toxin Reference Antibody (Suvratoxumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290552026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34029-1-sds-page.jpgAnti-Staphylococcus aureus alpha toxin Reference Antibody (Tosatoxumab)Anti-Staphylococcus aureus alpha toxin Reference Antibody (Tosatoxumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34029-1-sec-hplc.jpgAnti-Staphylococcus aureus alpha toxin Reference Antibody (Tosatoxumab)The purity of Anti-Staphylococcus aureus alpha toxin Reference Antibody (Tosatoxumab)is more than 100.00 % https://www.bosterbio.com/catalog/product/view/id/1290562026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-1-sds-page.jpgAnti-Zaire Ebola virus Reference Antibody (Porgaviximab)Anti-Zaire Ebola virus Reference Antibody (Porgaviximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-1-sec-hplc.jpgAnti-Zaire Ebola virus Reference Antibody (Porgaviximab)The purity of Anti-Zaire Ebola virus Reference Antibody (Porgaviximab)is more than 98% https://www.bosterbio.com/catalog/product/view/id/1290572026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08425-1-sds-page.jpgAnti-SARS-CoV-2 Reference Antibody (Adintrevimab)Anti-SARS-CoV-2 Reference Antibody (Adintrevimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/0/m08425-1-sec-hplc.jpgAnti-SARS-CoV-2 Reference Antibody (Adintrevimab)The purity of Anti-SARS-CoV-2 Reference Antibody (Adintrevimab)is more than 96.94% https://www.bosterbio.com/catalog/product/view/id/1290582026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-3-sds-page.jpgAnti-IgE (M1 prime) Reference Antibody (quilizumab)Anti-IgE (M1 prime) Reference Antibody (quilizumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34013-3-sec-hplc.jpgAnti-IgE (M1 prime) Reference Antibody (quilizumab)The purity of Anti-IgE (M1 prime) Reference Antibody (quilizumab)is more than 97.29% https://www.bosterbio.com/catalog/product/view/id/1290592026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34032-sds-page.jpgAnti-158P1D7 Reference Antibody (Agensys patent anti-158P1D7)Anti-158P1D7 Reference Antibody (Agensys patent anti-158P1D7) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34032-sec-hplc.jpgAnti-158P1D7 Reference Antibody (Agensys patent anti-158P1D7)The purity of Anti-158P1D7 Reference Antibody (Agensys patent anti-158P1D7)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290602026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34033-sds-page.jpgAnti-Abm Reference Antibody ( IgG1+Kappa Isotype Control)Anti-Abm Reference Antibody ( IgG1+Kappa Isotype Control) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34033-sec-hplc.jpgAnti-Abm Reference Antibody ( IgG1+Kappa Isotype Control)The purity of Anti-Abm Reference Antibody ( IgG1+Kappa Isotype Control)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290612026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34033-1-sds-page.jpgAnti-Abm Reference Antibody ( IgG4+Kappa Isotype Control)Anti-Abm Reference Antibody ( IgG4+Kappa Isotype Control) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34033-1-sec-hplc.jpgAnti-Abm Reference Antibody ( IgG4+Kappa Isotype Control)The purity of Anti-Abm Reference Antibody ( IgG4+Kappa Isotype Control)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290622026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34024-2-sds-page.jpgAnti-CanAg Reference Antibody (Cantuzumab mertansine)Anti-CanAg Reference Antibody (Cantuzumab mertansine) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34024-2-sec-hplc.jpgAnti-CanAg Reference Antibody (Cantuzumab mertansine)The purity of Anti-CanAg Reference Antibody (Cantuzumab mertansine)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290632026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34030-sds-page.jpgAnti-Cdiff Toxin A Reference Antibody (actoxumab)Anti-Cdiff Toxin A Reference Antibody (actoxumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34030-sec-hplc.jpgAnti-Cdiff Toxin A Reference Antibody (actoxumab)The purity of Anti-Cdiff Toxin A Reference Antibody (actoxumab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290642026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34034-sds-page.jpgAnti-CXC-ELR Reference Antibody (Lilly patent anti-Pan-ELR+)Anti-CXC-ELR Reference Antibody (Lilly patent anti-Pan-ELR+) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34034-sec-hplc.jpgAnti-CXC-ELR Reference Antibody (Lilly patent anti-Pan-ELR+)The purity of Anti-CXC-ELR Reference Antibody (Lilly patent anti-Pan-ELR+)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290652026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34019-2-sds-page.jpgAnti-GD2 Reference Antibody (EMD 273063)Anti-GD2 Reference Antibody (EMD 273063) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34019-2-sec-hplc.jpgAnti-GD2 Reference Antibody (EMD 273063)The purity of Anti-GD2 Reference Antibody (EMD 273063)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290662026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34023-1-sds-page.jpgAnti-GD3 Reference Antibody (ecromeximab-MMAE)Anti-GD3 Reference Antibody (ecromeximab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34023-1-sec-hplc.jpgAnti-GD3 Reference Antibody (ecromeximab-MMAE)The purity of Anti-GD3 Reference Antibody (ecromeximab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290672026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34038-sds-page.jpgAnti-HA Reference Antibody (Navivumab)Anti-HA Reference Antibody (Navivumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34038-sec-hplc.jpgAnti-HA Reference Antibody (Navivumab)The purity of Anti-HA Reference Antibody (Navivumab)is more than 99.1% https://www.bosterbio.com/catalog/product/view/id/1290682026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34038-1-sds-page.jpgAnti-IAV HA Reference AntibodyAnti-IAV HA Reference Antibody on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34038-1-sec-hplc.jpgAnti-IAV HA Reference AntibodyThe purity of Anti-IAV HA Reference Antibodyis more than 95% https://www.bosterbio.com/catalog/product/view/id/1290692026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34039-sds-page.jpgAnti-IAV Reference Antibody Anti-IAV Reference Antibody on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34039-sec-hplc.jpgAnti-IAV Reference Antibody The purity of Anti-IAV Reference Antibody is more than 95.11% https://www.bosterbio.com/catalog/product/view/id/1290702026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34040-sds-page.jpgAnti-Meflin Reference Antibody (Tokai U. Patent Anti-Meflin)Anti-Meflin Reference Antibody (Tokai U. Patent Anti-Meflin) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34040-sec-hplc.jpgAnti-Meflin Reference Antibody (Tokai U. Patent Anti-Meflin)The purity of Anti-Meflin Reference Antibody (Tokai U. Patent Anti-Meflin)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290712026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34025-1-sds-page.jpgAnti-MU5AC Reference Antibody (ensituximab-MMAE)Anti-MU5AC Reference Antibody (ensituximab-MMAE) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34025-1-sec-hplc.jpgAnti-MU5AC Reference Antibody (ensituximab-MMAE)The purity of Anti-MU5AC Reference Antibody (ensituximab-MMAE)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290722026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34020-1-sds-page.jpgAnti-oxLDL Reference Antibody (Okayama U. patent anti-oxLDL)Anti-oxLDL Reference Antibody (Okayama U. patent anti-oxLDL) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34020-1-sec-hplc.jpgAnti-oxLDL Reference Antibody (Okayama U. patent anti-oxLDL)The purity of Anti-oxLDL Reference Antibody (Okayama U. patent anti-oxLDL)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290732026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34037-sds-page.jpgAnti-PCLA Reference Antibody (U.Penn. patent anti-PCLA)Anti-PCLA Reference Antibody (U.Penn. patent anti-PCLA) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90% https://www.bosterbio.com/catalog/product/view/id/1290742026-03-10T04:39:46+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34026-1-sds-page.jpgAnti-Rabies virus GP Reference Antibody (rafivirumab)Anti-Rabies virus GP Reference Antibody (rafivirumab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34026-1-sec-hplc.jpgAnti-Rabies virus GP Reference Antibody (rafivirumab)The purity of Anti-Rabies virus GP Reference Antibody (rafivirumab)is more than 98.43% https://www.bosterbio.com/catalog/product/view/id/1290752026-03-10T04:39:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34031-sds-page.jpgAnti-Shiga toxin (E.coli) Reference Antibody (pritoxaximab)Anti-Shiga toxin (E.coli) Reference Antibody (pritoxaximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34031-sec-hplc.jpgAnti-Shiga toxin (E.coli) Reference Antibody (pritoxaximab)The purity of Anti-Shiga toxin (E.coli) Reference Antibody (pritoxaximab)is more than 100.00% https://www.bosterbio.com/catalog/product/view/id/1290762026-03-10T04:39:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34031-1-sds-page.jpgAnti-Shiga toxin (E.coli) Reference Antibody (setoxaximab)Anti-Shiga toxin (E.coli) Reference Antibody (setoxaximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34031-1-sec-hplc.jpgAnti-Shiga toxin (E.coli) Reference Antibody (setoxaximab)The purity of Anti-Shiga toxin (E.coli) Reference Antibody (setoxaximab)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290772026-03-10T04:39:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34035-sds-page.jpgAnti-STOP1 Reference Antibody (Genentech patent anti-STOP-1)Anti-STOP1 Reference Antibody (Genentech patent anti-STOP-1) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34035-sec-hplc.jpgAnti-STOP1 Reference Antibody (Genentech patent anti-STOP-1)The purity of Anti-STOP1 Reference Antibody (Genentech patent anti-STOP-1)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290782026-03-10T04:39:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34036-sds-page.jpgAnti-TAT226 Reference Antibody (Genentech patent anti-TAT226)Anti-TAT226 Reference Antibody (Genentech patent anti-TAT226) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34036-sec-hplc.jpgAnti-TAT226 Reference Antibody (Genentech patent anti-TAT226)The purity of Anti-TAT226 Reference Antibody (Genentech patent anti-TAT226)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290792026-03-10T04:39:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34015-1-sds-page.jpgAnti-TCR Reference Antibody (NKTT320)Anti-TCR Reference Antibody (NKTT320) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34015-1-sec-hplc.jpgAnti-TCR Reference Antibody (NKTT320)The purity of Anti-TCR Reference Antibody (NKTT320)is more than 95% https://www.bosterbio.com/catalog/product/view/id/1290802026-03-10T04:39:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-2-sds-page.jpgAnti-Zaire Ebola virus Reference Antibody (Cosfroviximab)Anti-Zaire Ebola virus Reference Antibody (Cosfroviximab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-2-sec-hplc.jpgAnti-Zaire Ebola virus Reference Antibody (Cosfroviximab)The purity of Anti-Zaire Ebola virus Reference Antibody (Cosfroviximab)is more than 98.99% https://www.bosterbio.com/catalog/product/view/id/1290812026-03-10T04:39:47+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-3-sds-page.jpgAnti-Zaire Ebola virus Reference Antibody (Odesivimab)Anti-Zaire Ebola virus Reference Antibody (Odesivimab) on SDS-PAGE under reducing (R) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 95%https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/m/3/m34022-3-sec-hplc.jpgAnti-Zaire Ebola virus Reference Antibody (Odesivimab)The purity of Anti-Zaire Ebola virus Reference Antibody (Odesivimab)is more than 99.64% https://www.bosterbio.com/catalog/product/view/id/1290822026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02514-2-ctss-primary-antibodies-wb-testing-1.jpgAnti-CTSS Antibody Picoband® Western blot analysis of CTSS using anti-CTSS antibody (A02514-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-CTSS antigen affinity purified polyclonal antibody (A02514-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for CTSS at approximately 25 kDa. The expected band size for CTSS is at 37 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02514-2-ctss-primary-antibodies-fcm-testing-2.jpgAnti-CTSS Antibody Picoband® Flow Cytometry analysis of THP-1 cells using anti-CTSS antibody (A02514-2). Overlay histogram showing THP-1 cells stained with A02514-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-CTSS Antibody (A02514-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290832026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03397-ncoa6-primary-antibodies-wb-testing-1.jpgAnti-NCOA6 Antibody Picoband® Western blot analysis of NCOA6 using anti-NCOA6 antibody (A03397). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hacat whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NCOA6 antigen affinity purified polyclonal antibody (A03397) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NCOA6 at approximately 250 kDa. The expected band size for NCOA6 is at 219 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03397-ncoa6-primary-antibodies-if-testing-2.jpgAnti-NCOA6 Antibody Picoband® IF analysis of NCOA6 using anti-NCOA6 antibody (A03397) and anti-Beta Tubulin antibody (M01857-3). NCOA6 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-NCOA6 Antibody (A03397) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight?594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03397-ncoa6-primary-antibodies-fcm-testing-3.jpgAnti-NCOA6 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-NCOA6 antibody (A03397). Overlay histogram showing A431 cells stained with A03397 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NCOA6 Antibody (A03397, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290842026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14058-2-nudt18-primary-antibodies-wb-testing-1.jpgAnti-NUDT18 Antibody Picoband® Western blot analysis of NUDT18 using anti-NUDT18 antibody (A14058-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat C6 whole cell lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-NUDT18 antigen affinity purified polyclonal antibody (A14058-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for NUDT18 at approximately 36 kDa. The expected band size for NUDT18 is at 36 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14058-2-nudt18-primary-antibodies-fcm-testing-2.jpgAnti-NUDT18 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-NUDT18 antibody (A14058-2). Overlay histogram showing Jurkat cells stained with A14058-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-NUDT18 Antibody (A14058-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290852026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09716-1-reps2-primary-antibodies-wb-testing-1.jpgAnti-REPS2 Antibody Picoband® Western blot analysis of REPS2 using anti-REPS2 antibody (A09716-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat brain tissue lysates, Lane 2: rat NRK whole cell lysates, Lane 3: mouse brain tissue lysates, Lane 4: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-REPS2 antigen affinity purified polyclonal antibody (A09716-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for REPS2 at approximately 72 kDa. The expected band size for REPS2 is at 72 kDa. https://www.bosterbio.com/catalog/product/view/id/1290862026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08369-1-garnl1-ralgapa1-primary-antibodies-wb-testing-1.jpgAnti-GARNL1/RALGAPA1 Antibody Picoband® Western blot analysis of GARNL1/RALGAPA1 using anti-GARNL1/RALGAPA1 antibody (A08369-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse brain tissue lysates, Lane 5: mouse Neuro-2a whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-GARNL1/RALGAPA1 antigen affinity purified polyclonal antibody (A08369-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for GARNL1/RALGAPA1 at approximately 250 kDa. The expected band size for GARNL1/RALGAPA1 is at 230 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08369-1-garnl1-ralgapa1-primary-antibodies-fcm-testing-2.jpgAnti-GARNL1/RALGAPA1 Antibody Picoband® Flow Cytometry analysis of SH-SY5Y cells using anti-GARNL1/RALGAPA1 antibody (A08369-1). Overlay histogram showing SH-SY5Y cells stained with A08369-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-GARNL1/RALGAPA1 Antibody (A08369-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290872026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31823-2-c14orf166-rtraf-primary-antibodies-wb-testing-1.jpgAnti-C14orf166/RTRAF Antibody Picoband® Western blot analysis of C14orf166/RTRAF using anti-C14orf166/RTRAF antibody (A31823-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human PC-3 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human SIHA whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat heart tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C14orf166/RTRAF antigen affinity purified polyclonal antibody (A31823-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for C14orf166/RTRAF at approximately 28 kDa. The expected band size for C14orf166/RTRAF is at 28 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31823-2-c14orf166-rtraf-primary-antibodies-ihc-testing-2.jpgAnti-C14orf166/RTRAF Antibody Picoband® IHC analysis of C14orf166/RTRAF using anti-C14orf166/RTRAF antibody (A31823-2). C14orf166/RTRAF was detected in a paraffin-embedded section of human ovarian cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C14orf166/RTRAF Antibody (A31823-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31823-2-c14orf166-rtraf-primary-antibodies-ihc-testing-3.jpgAnti-C14orf166/RTRAF Antibody Picoband® IHC analysis of C14orf166/RTRAF using anti-C14orf166/RTRAF antibody (A31823-2). C14orf166/RTRAF was detected in a paraffin-embedded section of human lung cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C14orf166/RTRAF Antibody (A31823-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31823-2-c14orf166-rtraf-primary-antibodies-ihc-testing-4.jpgAnti-C14orf166/RTRAF Antibody Picoband® IHC analysis of C14orf166/RTRAF using anti-C14orf166/RTRAF antibody (A31823-2). C14orf166/RTRAF was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C14orf166/RTRAF Antibody (A31823-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31823-2-c14orf166-rtraf-primary-antibodies-ihc-testing-5.jpgAnti-C14orf166/RTRAF Antibody Picoband® IHC analysis of C14orf166/RTRAF using anti-C14orf166/RTRAF antibody (A31823-2). C14orf166/RTRAF was detected in a paraffin-embedded section of human tonsil tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C14orf166/RTRAF Antibody (A31823-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31823-2-c14orf166-rtraf-primary-antibodies-ihc-testing-6.jpgAnti-C14orf166/RTRAF Antibody Picoband® IHC analysis of C14orf166/RTRAF using anti-C14orf166/RTRAF antibody (A31823-2). C14orf166/RTRAF was detected in a paraffin-embedded section of human prostate cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-C14orf166/RTRAF Antibody (A31823-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/3/a31823-2-c14orf166-rtraf-primary-antibodies-if-testing-7.jpgAnti-C14orf166/RTRAF Antibody Picoband® IF analysis of C14orf166/RTRAF using anti-C14orf166/RTRAF antibody (A31823-2) and anti-Beta Tubulin antibody (M01857-3). C14orf166/RTRAF was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-C14orf166/RTRAF Antibody (A31823-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight?594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1290882026-03-17T05:16:24+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11986-1-c1orf103-lrif1-primary-antibodies-wb-testing-1.jpgAnti-C1orf103/LRIF1 Antibody Picoband® Western blot analysis of C1orf103/LRIF1 using anti-C1orf103/LRIF1 antibody (A11986-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-C1orf103/LRIF1 antigen affinity purified polyclonal antibody (A11986-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for C1orf103/LRIF1 at approximately 85 kDa. The expected band size for C1orf103/LRIF1 is at 85 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11986-1-c1orf103-lrif1-primary-antibodies-if-testing-2.jpgAnti-C1orf103/LRIF1 Antibody Picoband® IF analysis of C1orf103/LRIF1 using anti-C1orf103/LRIF1 antibody (A11986-1) and anti-Beta Tubulin antibody (M01857-3). C1orf103/LRIF1 was detected in an immunocytochemical section of A549 cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-C1orf103/LRIF1 Antibody (A11986-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight?594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11986-1-c1orf103-lrif1-primary-antibodies-fcm-testing-3.jpgAnti-C1orf103/LRIF1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-C1orf103/LRIF1 antibody (A11986-1). Overlay histogram showing HEL cells stained with A11986-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-C1orf103/LRIF1 Antibody (A11986-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290892026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04973-1-edem1-primary-antibodies-wb-testing-1.jpgAnti-EDEM1 Antibody Picoband® Western blot analysis of EDEM1 using anti-EDEM1 antibody (A04973-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human THP-1 whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EDEM1 antigen affinity purified polyclonal antibody (A04973-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EDEM1 at approximately 66 kDa. The expected band size for EDEM1 is at 74 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04973-1-edem1-primary-antibodies-fcm-testing-2.jpgAnti-EDEM1 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-EDEM1 antibody (A04973-1). Overlay histogram showing HEL cells stained with A04973-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EDEM1 Antibody (A04973-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290902026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04026-2-bop1-primary-antibodies-wb-testing-1.jpgAnti-BOP1 Antibody Picoband® Western blot analysis of BOP1 using anti-BOP1 antibody (A04026-2). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human PC-3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-BOP1 antigen affinity purified polyclonal antibody (A04026-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for BOP1 at approximately 110 kDa. The expected band size for BOP1 is at 84 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04026-2-bop1-primary-antibodies-if-testing-2.jpgAnti-BOP1 Antibody Picoband® IF analysis of BOP1 using anti-BOP1 antibody (A04026-2) and anti-Beta Tubulin antibody (M01857-3). BOP1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-BOP1 Antibody (A04026-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight?594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04026-2-bop1-primary-antibodies-fcm-testing-3.jpgAnti-BOP1 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-BOP1 antibody (A04026-2). Overlay histogram showing CACO-2 cells stained with A04026-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-BOP1 Antibody (A04026-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290912026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01535-2-dkc1-primary-antibodies-wb-testing-1.jpgAnti-DKC1 Antibody Picoband® Western blot analysis of DKC1 using anti-DKC1 antibody (A01535-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human U251 whole cell lysates, Lane 3: human A431 whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DKC1 antigen affinity purified polyclonal antibody (A01535-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DKC1 at approximately 58 kDa. The expected band size for DKC1 is at 58 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01535-2-dkc1-primary-antibodies-ihc-testing-2.jpgAnti-DKC1 Antibody Picoband® IHC analysis of DKC1 using anti-DKC1 antibody (A01535-2). DKC1 was detected in a paraffin-embedded section of human breast cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DKC1 Antibody (A01535-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01535-2-dkc1-primary-antibodies-ihc-testing-3.jpgAnti-DKC1 Antibody Picoband® IHC analysis of DKC1 using anti-DKC1 antibody (A01535-2). DKC1 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DKC1 Antibody (A01535-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01535-2-dkc1-primary-antibodies-ihc-testing-4.jpgAnti-DKC1 Antibody Picoband® IHC analysis of DKC1 using anti-DKC1 antibody (A01535-2). DKC1 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DKC1 Antibody (A01535-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01535-2-dkc1-primary-antibodies-if-testing-5.jpgAnti-DKC1 Antibody Picoband® IF analysis of DKC1 using anti-DKC1 antibody (A01535-2) and anti-Beta Tubulin antibody (M01857-3). DKC1 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-DKC1 Antibody (A01535-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) and DyLight?594 Conjugated Goat Anti-Mouse IgG (BA1141) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01535-2-dkc1-primary-antibodies-fcm-testing-6.jpgAnti-DKC1 Antibody Picoband® Flow Cytometry analysis of A431 cells using anti-DKC1 antibody (A01535-2). Overlay histogram showing A431 cells stained with A01535-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-DKC1 Antibody (A01535-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290922026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01771-1-dock8-primary-antibodies-wb-testing-1.jpgAnti-DOCK8 Antibody Picoband® Western blot analysis of DOCK8 using anti-DOCK8 antibody (A01771-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DOCK8 antigen affinity purified polyclonal antibody (A01771-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DOCK8 at approximately 230 kDa. The expected band size for DOCK8 is at 239 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01771-1-dock8-primary-antibodies-ihc-testing-2.jpgAnti-DOCK8 Antibody Picoband® IHC analysis of DOCK8 using anti-DOCK8 antibody (A01771-1). DOCK8 was detected in a paraffin-embedded section of mouse bone marrow tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DOCK8 Antibody (A01771-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01771-1-dock8-primary-antibodies-ihc-testing-3.jpgAnti-DOCK8 Antibody Picoband® IHC analysis of DOCK8 using anti-DOCK8 antibody (A01771-1). DOCK8 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-DOCK8 Antibody (A01771-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01771-1-dock8-primary-antibodies-fcm-testing-4.jpgAnti-DOCK8 Antibody Picoband® Flow Cytometry analysis of Raji cells using anti-DOCK8 antibody (A01771-1). Overlay histogram showing Raji cells stained with A01771-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-DOCK8 Antibody (A01771-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290932026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01509-1-dysbindin-dtnbp1-primary-antibodies-wb-testing-1.jpgAnti-Dysbindin/DTNBP1 Antibody Picoband® Western blot analysis of Dysbindin/DTNBP1 using anti-Dysbindin/DTNBP1 antibody (A01509-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SHSY-5Y whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: human Hela whole cell lysates, Lane 4: human Jurkat whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: rat testis tissue lysates, Lane 7: mouse brain tissue lysates, Lane 8: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Dysbindin/DTNBP1 antigen affinity purified polyclonal antibody (A01509-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Dysbindin/DTNBP1 at approximately 50 kDa. The expected band size for Dysbindin/DTNBP1 is at 39 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a01509-1-dysbindin-dtnbp1-primary-antibodies-fcm-testing-2.jpgAnti-Dysbindin/DTNBP1 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-Dysbindin/DTNBP1 antibody (A01509-1). Overlay histogram showing Jurkat cells stained with A01509-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-Dysbindin/DTNBP1 Antibody (A01509-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290942026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07823-2-elp2-primary-antibodies-wb-testing-1.jpgAnti-ELP2 Antibody Picoband® Western blot analysis of ELP2 using anti-ELP2 antibody (A07823-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human MCF-7 whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human HUVEC whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ELP2 antigen affinity purified polyclonal antibody (A07823-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ELP2 at approximately 93 kDa. The expected band size for ELP2 is at 93 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07823-2-elp2-primary-antibodies-if-testing-2.jpgAnti-ELP2 Antibody Picoband® IF analysis of ELP2 using anti-ELP2 antibody (A07823-2). ELP2 was detected in an immunocytochemical section of Hela cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-ELP2 Antibody (A07823-2) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a07823-2-elp2-primary-antibodies-fcm-testing-3.jpgAnti-ELP2 Antibody Picoband® Flow Cytometry analysis of K562 cells using anti-ELP2 antibody (A07823-2). Overlay histogram showing K562 cells stained with A07823-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-ELP2 Antibody (A07823-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290952026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05656-1-eif3h-primary-antibodies-wb-testing-1.jpgAnti-EIF3H Antibody Picoband® Western blot analysis of EIF3H using anti-EIF3H antibody (A05656-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human K562 whole cell lysates, Lane 3: human THP-1 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-EIF3H antigen affinity purified polyclonal antibody (A05656-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for EIF3H at approximately 40 kDa. The expected band size for EIF3H is at 40 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05656-1-eif3h-primary-antibodies-ihc-testing-2.jpgAnti-EIF3H Antibody Picoband® IHC analysis of EIF3H using anti-EIF3H antibody (A05656-1). EIF3H was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3H Antibody (A05656-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05656-1-eif3h-primary-antibodies-ihc-testing-3.jpgAnti-EIF3H Antibody Picoband® IHC analysis of EIF3H using anti-EIF3H antibody (A05656-1). EIF3H was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3H Antibody (A05656-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05656-1-eif3h-primary-antibodies-ihc-testing-4.jpgAnti-EIF3H Antibody Picoband® IHC analysis of EIF3H using anti-EIF3H antibody (A05656-1). EIF3H was detected in a paraffin-embedded section of rat bladder tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-EIF3H Antibody (A05656-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a05656-1-eif3h-primary-antibodies-fcm-testing-5.jpgAnti-EIF3H Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-EIF3H antibody (A05656-1). Overlay histogram showing PC-3 cells stained with A05656-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-EIF3H Antibody (A05656-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290962026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00797-2-dmpk-primary-antibodies-wb-testing-1.jpgAnti-DMPK Antibody Picoband® Western blot analysis of DMPK using anti-DMPK antibody (A00797-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat heart tissue lysates, Lane 2: rat skeletal muscle tissue lysates, Lane 3: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-DMPK antigen affinity purified polyclonal antibody (A00797-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for DMPK at approximately 70 kDa. The expected band size for DMPK is at 69 kDa. https://www.bosterbio.com/catalog/product/view/id/1290972026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-2-fbxo7-primary-antibodies-wb-testing-1.jpgAnti-FBXO7 Antibody Picoband® Western blot analysis of FBXO7 using anti-FBXO7 antibody (A04086-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HUVEC whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: human 293T whole cell lysates, Lane 5: rat lung tissue lysates, Lane 6: rat small intestine tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FBXO7 antigen affinity purified polyclonal antibody (A04086-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FBXO7 at approximately 59, 72 kDa. The expected band size for FBXO7 is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-2-fbxo7-primary-antibodies-ihc-testing-2.jpgAnti-FBXO7 Antibody Picoband® IHC analysis of FBXO7 using anti-FBXO7 antibody (A04086-2). FBXO7 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FBXO7 Antibody (A04086-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-2-fbxo7-primary-antibodies-ihc-testing-3.jpgAnti-FBXO7 Antibody Picoband® IHC analysis of FBXO7 using anti-FBXO7 antibody (A04086-2). FBXO7 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FBXO7 Antibody (A04086-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-2-fbxo7-primary-antibodies-ihc-testing-4.jpgAnti-FBXO7 Antibody Picoband® IHC analysis of FBXO7 using anti-FBXO7 antibody (A04086-2). FBXO7 was detected in a paraffin-embedded section of human endometrial cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FBXO7 Antibody (A04086-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-2-fbxo7-primary-antibodies-if-testing-5.jpgAnti-FBXO7 Antibody Picoband® IF analysis of FBXO7 using anti-FBXO7 antibody (A04086-2) and anti-Beta Tubulin antibody (M01857-3). FBXO7 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-FBXO7 Antibody (A04086-2) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight?488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-2-fbxo7-primary-antibodies-ip-testing-6.jpgAnti-FBXO7 Antibody Picoband® Immunoprecipitating FBXO7 in HepG2 whole cell lysate. Western blot analysis of FBXO7 using anti-FBXO7 antibody (A04086-2). Lane 1: HepG2 whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-FBXO7 antibody in HepG2 whole cell lysate, Lane 3: anti-FBXO7 antibody (2μg) + HepG2 whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-FBXO7 antigen affinity purified polyclonal antibody (A04086-2) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for FBXO7 at approximately 59-72 kDa. The expected band size for FBXO7 is at 59 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04086-2-fbxo7-primary-antibodies-fcm-testing-7.jpgAnti-FBXO7 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-FBXO7 antibody (A04086-2). Overlay histogram showing HepG2 cells stained with A04086-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FBXO7 Antibody (A04086-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1290982026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06760-1-fbxw8-primary-antibodies-wb-testing-1.jpgAnti-FBXW8 Antibody Picoband® Western blot analysis of FBXW8 using anti-FBXW8 antibody (A06760-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human A549 whole cell lysates, Lane 4: rat small intestine tissue lysates, Lane 5: rat lung tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FBXW8 antigen affinity purified polyclonal antibody (A06760-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FBXW8 at approximately 67 kDa. The expected band size for FBXW8 is at 67 kDa. https://www.bosterbio.com/catalog/product/view/id/1290992026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06691-1-fyco1-primary-antibodies-wb-testing-1.jpgAnti-FYCO1 Antibody Picoband® Western blot analysis of FYCO1 using anti-FYCO1 antibody (A06691-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HUVEC whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: rat testis tissue lysates, Lane 4: mouse heart tissue lysates, Lane 5: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FYCO1 antigen affinity purified polyclonal antibody (A06691-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FYCO1 at approximately 167 kDa. The expected band size for FYCO1 is at 167 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06691-1-fyco1-primary-antibodies-ihc-testing-2.jpgAnti-FYCO1 Antibody Picoband® IHC analysis of FYCO1 using anti-FYCO1 antibody (A06691-1). FYCO1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FYCO1 Antibody (A06691-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06691-1-fyco1-primary-antibodies-fcm-testing-3.jpgAnti-FYCO1 Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-FYCO1 antibody (A06691-1). Overlay histogram showing Jurkat cells stained with A06691-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FYCO1 Antibody (A06691-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291002026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00925-2-fasl-faslg-primary-antibodies-wb-testing-1.jpgAnti-FASL/FASLG Antibody Picoband® Western blot analysis of FASL/FASLG using anti-FASL/FASLG antibody (A00925-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FASL/FASLG antigen affinity purified polyclonal antibody (A00925-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FASL/FASLG at approximately 31 kDa. The expected band size for FASL/FASLG is at 31 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a00925-2-fasl-faslg-primary-antibodies-fcm-testing-2.jpgAnti-FASL/FASLG Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-FASL/FASLG antibody (A00925-2). Overlay histogram showing Jurkat cells stained with A00925-2 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-FASL/FASLG Antibody (A00925-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291012026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06536-espn-primary-antibodies-wb-testing-1.jpgAnti-ESPN Antibody Picoband® Western blot analysis of ESPN using anti-ESPN antibody (A06536). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat testis tissue lysates, Lane 2: mouse testis tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-ESPN antigen affinity purified polyclonal antibody (A06536) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for ESPN at approximately 110 kDa. The expected band size for ESPN is at 92 kDa. https://www.bosterbio.com/catalog/product/view/id/1291022026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a10673-2-pou6f2-primary-antibodies-wb-testing-1.jpgAnti-POU6F2 Antibody Picoband® Western blot analysis of POU6F2 using anti-POU6F2 antibody (A10673-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: rat testis tissue lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse testis tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-POU6F2 antigen affinity purified polyclonal antibody (A10673-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for POU6F2 at approximately 73 kDa. The expected band size for POU6F2 is at 73 kDa. https://www.bosterbio.com/catalog/product/view/id/1291032026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03058-2-iaspp-ppp1r13l-primary-antibodies-wb-testing-1.jpgAnti-iASPP/PPP1R13L Antibody Picoband® Western blot analysis of iASPP/PPP1R13L using anti-iASPP/PPP1R13L antibody (A03058-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human RT4 whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human U20S whole cell lysates, Lane 5: rat heart tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-iASPP/PPP1R13L antigen affinity purified polyclonal antibody (A03058-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for iASPP/PPP1R13L at approximately 110 kDa. The expected band size for iASPP/PPP1R13L is at 89 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a03058-2-iaspp-ppp1r13l-primary-antibodies-fcm-testing-2.jpgAnti-iASPP/PPP1R13L Antibody Picoband® Flow Cytometry analysis of U20S cells using anti-iASPP/PPP1R13L antibody (A03058-2). Overlay histogram showing U20S cells stained with A03058-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-iASPP/PPP1R13L Antibody (A03058-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291042026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08462-3-minpp1-primary-antibodies-wb-testing-1.jpgAnti-MINPP1 Antibody Picoband® Western blot analysis of MINPP1 using anti-MINPP1 antibody (A08462-3). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human HEL whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human A549 whole cell lysates, Lane 5: rat liver tissue lysates, Lane 6: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MINPP1 antigen affinity purified polyclonal antibody (A08462-3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MINPP1 at approximately 47 kDa. The expected band size for MINPP1 is at 55 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08462-3-minpp1-primary-antibodies-ihc-testing-2.jpgAnti-MINPP1 Antibody Picoband® IHC analysis of MINPP1 using anti-MINPP1 antibody (A08462-3). MINPP1 was detected in a paraffin-embedded section of rat kidney tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MINPP1 Antibody (A08462-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08462-3-minpp1-primary-antibodies-ihc-testing-3.jpgAnti-MINPP1 Antibody Picoband® IHC analysis of MINPP1 using anti-MINPP1 antibody (A08462-3). MINPP1 was detected in a paraffin-embedded section of human thyroid cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-MINPP1 Antibody (A08462-3) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08462-3-minpp1-primary-antibodies-fcm-testing-4.jpgAnti-MINPP1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-MINPP1 antibody (A08462-3). Overlay histogram showing 293T cells stained with A08462-3 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MINPP1 Antibody (A08462-3, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291052026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04139-1-myo1e-primary-antibodies-wb-testing-1.jpgAnti-MYO1E Antibody Picoband® Western blot analysis of MYO1E using anti-MYO1E antibody (A04139-1). Electrophoresis was performed on a 8% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human A549 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MYO1E antigen affinity purified polyclonal antibody (A04139-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MYO1E at approximately 127 kDa. The expected band size for MYO1E is at 127 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a04139-1-myo1e-primary-antibodies-fcm-testing-2.jpgAnti-MYO1E Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-MYO1E antibody (A04139-1). Overlay histogram showing Jurkat cells stained with A04139-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MYO1E Antibody (A04139-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291062026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02060-1-masp1-primary-antibodies-wb-testing-1.jpgAnti-MASP1 Antibody Picoband® Western blot analysis of MASP1 using anti-MASP1 antibody (A02060-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: rat liver tissue lysates, Lane 3: rat brain tissue lysates, Lane 4: mouse liver tissue lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse HEPA1-6 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MASP1 antigen affinity purified polyclonal antibody (A02060-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MASP1 at approximately 79 kDa. The expected band size for MASP1 is at 79 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a02060-1-masp1-primary-antibodies-fcm-testing-2.jpgAnti-MASP1 Antibody Picoband® Flow Cytometry analysis of PC-3 cells using anti-MASP1 antibody (A02060-1). Overlay histogram showing PC-3 cells stained with A02060-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-MASP1 Antibody (A02060-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291072026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08501-1-mcmbp-primary-antibodies-wb-testing-1.jpgAnti-MCMBP Antibody Picoband® Western blot analysis of MCMBP using anti-MCMBP antibody (A08501-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human 293T whole cell lysates, Lane 4: human Hacat whole cell lysates, Lane 5: rat thymus tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse thymus tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MCMBP antigen affinity purified polyclonal antibody (A08501-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MCMBP at approximately 73 kDa. The expected band size for MCMBP is at 73 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08501-1-mcmbp-primary-antibodies-ip-testing-2.jpgAnti-MCMBP Antibody Picoband® Immunoprecipitating MCMBP in 293T whole cell lysate. Western blot analysis of MCMBP using anti-MCMBP antibody (A08501-1). Lane 1: 293T whole cell lysates (30ug), Lane 2: Rabbit control IgG instead of anti-MCMBP antibody in 293T whole cell lysate, Lane 3: anti-MCMBP antibody (2μg) + 293T whole cell lysate (500μg). After electrophoresis, proteins were transferred to a membrane. Then the membrane was incubated with rabbit anti-MCMBP antigen affinity purified polyclonal antibody (A08501-1) at a dilution of 0.5 μg/mL and probed with a goat anti-rabbit IgG-HRP secondary antibody (Catalog # BA1054). The signal is developed using ECL Plus Western Blotting Substrate (Catalog # AR1197). A specific band was detected for MCMBP at approximately 73 kDa. The expected band size for MCMBP is at 73 kDa. https://www.bosterbio.com/catalog/product/view/id/1291082026-03-17T05:16:25+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-2-fundc1-primary-antibodies-wb-testing-1.jpgAnti-FUNDC1 Antibody Picoband® Western blot analysis of FUNDC1 using anti-FUNDC1 antibody (A08688-2). Electrophoresis was performed on a 12% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SiHa whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat C6 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-FUNDC1 antigen affinity purified polyclonal antibody (A08688-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for FUNDC1 at approximately 17 kDa. The expected band size for FUNDC1 is at 17 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-2-fundc1-primary-antibodies-ihc-testing-2.jpgAnti-FUNDC1 Antibody Picoband® IHC analysis of FUNDC1 using anti-FUNDC1 antibody (A08688-2). FUNDC1 was detected in a paraffin-embedded section of human cervical cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FUNDC1 Antibody (A08688-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-2-fundc1-primary-antibodies-ihc-testing-3.jpgAnti-FUNDC1 Antibody Picoband® IHC analysis of FUNDC1 using anti-FUNDC1 antibody (A08688-2). FUNDC1 was detected in a paraffin-embedded section of mouse midbrain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FUNDC1 Antibody (A08688-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-2-fundc1-primary-antibodies-ihc-testing-4.jpgAnti-FUNDC1 Antibody Picoband® IHC analysis of FUNDC1 using anti-FUNDC1 antibody (A08688-2). FUNDC1 was detected in a paraffin-embedded section of human pancreas cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FUNDC1 Antibody (A08688-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-2-fundc1-primary-antibodies-ihc-testing-5.jpgAnti-FUNDC1 Antibody Picoband® IHC analysis of FUNDC1 using anti-FUNDC1 antibody (A08688-2). FUNDC1 was detected in a paraffin-embedded section of rat midbrain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-FUNDC1 Antibody (A08688-2) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08688-2-fundc1-primary-antibodies-fcm-testing-6.jpgAnti-FUNDC1 Antibody Picoband® Flow Cytometry analysis of SiHa cells using anti-FUNDC1 antibody (A08688-2). Overlay histogram showing SiHa cells stained with A08688-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-FUNDC1 Antibody (A08688-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291092026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11103-1-matrilin-4-matn4-primary-antibodies-wb-testing-1.jpgAnti-Matrilin-4/MATN4 Antibody Picoband® Western blot analysis of Matrilin-4/MATN4 using anti-Matrilin-4/MATN4 antibody (A11103-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human Jurkat whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Matrilin-4/MATN4 antigen affinity purified polyclonal antibody (A11103-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for Matrilin-4/MATN4 at approximately 68 kDa. The expected band size for Matrilin-4/MATN4 is at 68 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a11103-1-matrilin-4-matn4-primary-antibodies-fcm-testing-2.jpgAnti-Matrilin-4/MATN4 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-Matrilin-4/MATN4 antibody (A11103-1). Overlay histogram showing HEL cells stained with A11103-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-Matrilin-4/MATN4 Antibody (A11103-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291102026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12907-1-lmbr1l-primary-antibodies-wb-testing-1.jpgAnti-LMBR1L Antibody Picoband® Western blot analysis of LMBR1L using anti-LMBR1L antibody (A12907-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: rat liver tissue lysates, Lane 2: mouse liver tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMBR1L antigen affinity purified polyclonal antibody (A12907-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LMBR1L at approximately 57 kDa. The expected band size for LMBR1L is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a12907-1-lmbr1l-primary-antibodies-fcm-testing-2.jpgAnti-LMBR1L Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-LMBR1L antibody (A12907-1). Overlay histogram showing HepG2 cells stained with A12907-1 (Blue line). The cells were fixed with 4% paraformaldehyde and blocked with 10% normal goat serum. And then incubated with rabbit anti-LMBR1L Antibody (A12907-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291112026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18456-lmntd2-primary-antibodies-wb-testing-1.jpgAnti-LMNTD2 Antibody Picoband® Western blot analysis of LMNTD2 using anti-LMNTD2 antibody (A18456). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human Hacat whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human Hela whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat C6 whole cellue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse RAW264.7 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMNTD2 antigen affinity purified polyclonal antibody (A18456) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LMNTD2 at approximately 70 kDa. The expected band size for LMNTD2 is at 70 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18456-lmntd2-primary-antibodies-fcm-testing-2.jpgAnti-LMNTD2 Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-LMNTD2 antibody (A18456). Overlay histogram showing CACO-2 cells stained with A18456 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LMNTD2 Antibody (A18456, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18456-lmntd2-primary-antibodies-fcm-testing-3.jpgAnti-LMNTD2 Antibody Picoband® Flow Cytometry analysis of HEL cells using anti-LMNTD2 antibody (A18456). Overlay histogram showing HEL cells stained with A18456 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LMNTD2 Antibody (A18456, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291122026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09390-2-pip4k2b-primary-antibodies-wb-testing-1.jpgAnti-PIP4K2B Antibody Picoband® Western blot analysis of PIP4K2B using anti-PIP4K2B antibody (A09390-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Hela whole cell lysates, Lane 2: human 293T whole cell lysates, Lane 3: rat brain tissue lysates, Lane 4: rat PC-12 whole cellue lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse NIH/3T3 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIP4K2B antigen affinity purified polyclonal antibody (A09390-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PIP4K2B at approximately 50 kDa. The expected band size for PIP4K2B is at 47 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09390-2-pip4k2b-primary-antibodies-fcm-testing-2.jpgAnti-PIP4K2B Antibody Picoband® Flow Cytometry analysis of HeLa cells using anti-PIP4K2B antibody (A09390-2). Overlay histogram showing HeLa cells stained with A09390-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PIP4K2B Antibody (A09390-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291132026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08932-1-pip5k1b-primary-antibodies-wb-testing-1.jpgAnti-PIP5K1B Antibody Picoband® Western blot analysis of PIP5K1B using anti-PIP5K1B antibody (A08932-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human HepG2 whole cell lysates, Lane 3: human Caco-2 whole cell lysates, Lane 4: rat testis tissue lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse testis tissue lysates, Lane 7: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PIP5K1B antigen affinity purified polyclonal antibody (A08932-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PIP5K1B at approximately 62 kDa. The expected band size for PIP5K1B is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08932-1-pip5k1b-primary-antibodies-fcm-testing-2.jpgAnti-PIP5K1B Antibody Picoband® Flow Cytometry analysis of CACO-2 cells using anti-PIP5K1B antibody (A08932-1). Overlay histogram showing CACO-2 cells stained with A08932-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PIP5K1B Antibody (A08932-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291142026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a09816-1-plagl2-primary-antibodies-wb-testing-1.jpgAnti-PLAGL2 Antibody Picoband® Western blot analysis of PLAGL2 using anti-PLAGL2 antibody (A09816-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HEL whole cell lysates, Lane 2: human Caco-2 whole cell lysates, Lane 3: human HepG2 whole cell lysates, Lane 4: rat brain tissue lysates, Lane 5: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PLAGL2 antigen affinity purified polyclonal antibody (A09816-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PLAGL2 at approximately 50 kDa. The expected band size for PLAGL2 is at 55 kDa. https://www.bosterbio.com/catalog/product/view/id/1291152026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18010-phldb3-primary-antibodies-wb-testing-1.jpgAnti-PHLDB3 Antibody Picoband® Western blot analysis of PHLDB3 using anti-PHLDB3 antibody (A18010). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human Caco-2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: rat lung tissue lysates, Lane 4: rat kidney tissue lysates, Lane 5: mouse lung tissue lysates, Lane 6: mouse kidney tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-PHLDB3 antigen affinity purified polyclonal antibody (A18010) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for PHLDB3 at approximately 72 kDa. The expected band size for PHLDB3 is at 72 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18010-phldb3-primary-antibodies-ihc-testing-2.jpgAnti-PHLDB3 Antibody Picoband® IHC analysis of PHLDB3 using anti-PHLDB3 antibody (A18010). PHLDB3 was detected in a paraffin-embedded section of human esophageal cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-PHLDB3 Antibody (A18010) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a18010-phldb3-primary-antibodies-fcm-testing-3.jpgAnti-PHLDB3 Antibody Picoband® Flow Cytometry analysis of MCF-7 cells using anti-PHLDB3 antibody (A18010). Overlay histogram showing MCF-7 cells stained with A18010 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-PHLDB3 Antibody (A18010, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291162026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14225-2-mpnd-primary-antibodies-wb-testing-1.jpgAnti-MPND Antibody Picoband® Western blot analysis of MPND using anti-MPND antibody (A14225-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human HepG2 whole cell lysates, Lane 2: human MCF-7 whole cell lysates, Lane 3: human Jurkat whole cell lysates, Lane 4: human RT-4 whole cell lysates, Lane 5: rat brain tissue lysates, Lane 6: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-MPND antigen affinity purified polyclonal antibody (A14225-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for MPND at approximately 51 kDa. The expected band size for MPND is at 51 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a14225-2-mpnd-primary-antibodies-fcm-testing-2.jpgAnti-MPND Antibody Picoband® Flow Cytometry analysis of Jurkat cells using anti-MPND antibody (A14225-2). Overlay histogram showing Jurkat cells stained with A14225-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-MPND Antibody (A14225-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291172026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08163-1-lmbrd1-primary-antibodies-wb-testing-1.jpgAnti-LMBRD1 Antibody Picoband® Western blot analysis of LMBRD1 using anti-LMBRD1 antibody (A08163-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human 293T whole cell lysates, Lane 2: human RT4 whole cell lysates, Lane 3: human K562 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-LMBRD1 antigen affinity purified polyclonal antibody (A08163-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for LMBRD1 at approximately 61 kDa. The expected band size for LMBRD1 is at 61 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a08163-1-lmbrd1-primary-antibodies-fcm-testing-2.jpgAnti-LMBRD1 Antibody Picoband® Flow Cytometry analysis of 293T cells using anti-LMBRD1 antibody (A08163-1). Overlay histogram showing 293T cells stained with A08163-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-LMBRD1 Antibody (A08163-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight?488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1291222026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0430_1.pngHuman IL-17/IL-17A PicoKine&reg Quick ELISA KitHuman IL-17 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291232026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0389.pngHuman IL-1 Alpha/IL-1F1/IL1A PicoKine&reg Quick ELISA KitHuman IL-1 alpha PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291242026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0779_1.pngHuman IL-7/Interleukin-7 PicoKine&reg Quick ELISA KitHuman IL-7 PicoKine ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291252026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/f/e/fek0413_1.pngHuman IL-8/Interleukin-8/CXCL8 PicoKine&reg Quick ELISA KitHuman IL-8 PicoKine ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/anti-sea-lamprey-gamma-synuclein-antibody-dz41665-boster.html2026-03-10T04:39:49+00:00daily0.9 https://www.bosterbio.com/catalog/product/view/id/1291312026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0672.pngHuman Cathepsin D EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Cathepsin D EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291322026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0842.pngHuman TNFSF11/RANKL EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TNFSF11/RANKL EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291332026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1422.pngHuman CD73/NT5E/Ecto-5'-nucleotidase EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CD73/NT5E/Ecto-5'-nucleotidase EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291342026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0513.pngHuman TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291352026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0514.pngRat TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291362026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0515.pngMouse TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291372026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0513-bv.pngBovine TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Bovine TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291382026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0513-cn.pngDog Canine TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Dog Canine TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291392026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0513-po.pngPig porcine TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Pig porcine TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291402026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0513-pr.pngMonkey primate TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Monkey primate TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291412026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0513-rb.pngrabbit TGF Beta 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)rabbit TGF Beta 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291422026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1349.pngHuman JAM-A/F11R/Junctional Adhesion Molecule 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human JAM-A/F11R/Junctional Adhesion Molecule 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291432026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1702.pngHuman Haptoglobin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Haptoglobin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291442026-03-10T04:39:49+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0376.pngHuman IGF-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human IGF-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291452026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0376-bv.pngBovine IGF-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Bovine IGF-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291462026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0376-eq.pngHorse equine IGF-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Horse equine IGF-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291472026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0376-rb.pngrabbit IGF-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)rabbit IGF-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291482026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1220.pngHuman soluble CD5 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human soluble CD5 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291492026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1289.pngHuman REG-4 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human REG-4 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291502026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0831.pngHuman RBP4/Retinol Binding Protein 4 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human RBP4/Retinol Binding Protein 4 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291512026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1259.pngHuman Ficolin-3 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Ficolin-3 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291522026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2038.pngHuman TCN2/Transcobalamin-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TCN2/Transcobalamin-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291532026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0707.pngHuman B7-1/CD80 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human B7-1/CD80 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291542026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1208.pngMouse SAP/PTX2/APCS EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse SAP/PTX2/APCS EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291552026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1116.pngHuman IL-1 RL1/ST2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human IL-1 RL1/ST2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291562026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1414.pngMouse CD5L/CT-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CD5L/CT-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291572026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0521.pngMouse TIMP-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse TIMP-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291582026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1499.pngMouse Persephin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Persephin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291592026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1665.pngMouse CRLF2/TSLP R EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CRLF2/TSLP R EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291602026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0365.pngMouse GM-CSF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse GM-CSF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291612026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0562.pngMouse E-Cadherin/CDH1/Cadherin-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse E-Cadherin/CDH1/Cadherin-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291622026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0765.pngMouse Galectin-3/LGALS3 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Galectin-3/LGALS3 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291632026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0458.pngHuman MMP-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human MMP-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291642026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0311-bv.pngBovine BMP-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Bovine BMP-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291652026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0311-eq.pngHorse equine BMP-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Horse equine BMP-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291662026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0311-po.pngPig porcine BMP-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Pig porcine BMP-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291672026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0311-pr.pngMonkey primate BMP-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Monkey primate BMP-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291682026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0311-rb.pngrabbit BMP-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)rabbit BMP-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291692026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0313-cn.pngDog Canine BMP-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Dog Canine BMP-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291702026-03-10T04:39:50+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1281.pngRat RANK EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat RANK EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291712026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0541.pngMouse VEGF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse VEGF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291722026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1351.pngRat EPO/Erythropoietin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat EPO/Erythropoietin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291732026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0333.pngMouse EPO/Erythropoietin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse EPO/Erythropoietin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291742026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1760.pngHuman Endorepellin/HSPG2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Endorepellin/HSPG2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291752026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0363.pngRat GDNF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat GDNF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291762026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0935.pngMouse GDNF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse GDNF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291772026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0481.pngMouse OPG (TNFRSF11B)/Osteoprotegerin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse OPG (TNFRSF11B)/Osteoprotegerin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291782026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0936.pngRat sE-Selectin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat sE-Selectin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291792026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1743.pngHuman VWF-A2/VWF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human VWF-A2/VWF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291802026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0370.pngHuman ICAM-1/CD54 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human ICAM-1/CD54 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291812026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0395.pngHuman IL1R1/Il 1 Ri EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human IL1R1/Il 1 Ri EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291822026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1393.pngHuman Serpin C1/Antithrombin-III EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Serpin C1/Antithrombin-III EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291832026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0752.pngHuman ESM1/Endocan EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human ESM1/Endocan EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291842026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1280.pngHuman Granulysin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Granulysin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291852026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0426.pngHuman IL-15/Interleukin-15 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human IL-15/Interleukin-15 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291862026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1835.pngMouse REG3A EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse REG3A EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291872026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0400.pngHuman CD25/IL-2sR Alpha EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CD25/IL-2sR Alpha EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291882026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0974.pngHuman Chitinase 3-like 1/YKL-40 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Chitinase 3-like 1/YKL-40 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291892026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1425.pngHuman Caspase 3/CASP3 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Caspase 3/CASP3 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291902026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0863.pngMouse PLGF-2/PGF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse PLGF-2/PGF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291912026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0444.pngHuman M-CSF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human M-CSF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291922026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0663.pngHuman BAFF/TNFSF13B EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human BAFF/TNFSF13B EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291932026-03-10T04:39:51+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1781.pngMouse Contactin-4 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Contactin-4 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291942026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0919.pngMouse CXCL5/LIX/ENA-78/GCP 2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CXCL5/LIX/ENA-78/GCP 2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291952026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1320.pngHuman CD93/C1qR EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CD93/C1qR EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291962026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0446.pngHuman CCL22/MDC EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CCL22/MDC EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291972026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0568.pngMouse MCP-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse MCP-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291982026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0350.pngRat Fibronectin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat Fibronectin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1291992026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0351.pngMouse Fibronectin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Fibronectin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292002026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0484.pngHuman PDGF-AB EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human PDGF-AB EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292012026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0909.pngHuman Aggrecan/ACAN EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Aggrecan/ACAN EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292022026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0362.pngHuman GDNF/Glial Derived Neurotrophic Factor EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human GDNF/Glial Derived Neurotrophic Factor EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292032026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0506.pngMouse P-Selectin/CD62P EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse P-Selectin/CD62P EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292042026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1419.pngMouse CD44 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CD44 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292052026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1654.pngHuman Cystatin SN/CST1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Cystatin SN/CST1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292062026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1614.pngHuman Dystroglycan EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Dystroglycan EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292072026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0731.pngRat CXCL7/PPBP EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat CXCL7/PPBP EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292082026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1329.pngHuman Chemerin/RARRES2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Chemerin/RARRES2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292092026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0520.pngHuman TIMP-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TIMP-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292102026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0445.pngMouse M-CSF EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse M-CSF EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292112026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0805.pngHuman MBL2/MPB-C EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human MBL2/MPB-C EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292122026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0596.pngMouse Adiponectin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Adiponectin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292132026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1128.pngMouse CCL12/MCP5 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CCL12/MCP5 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292142026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1192.pngMouse Progranulin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Progranulin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292152026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0816.pngHuman Prostate-specific antigen EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Prostate-specific antigen EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292162026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0337.pngHuman FASL/CD95LG/CD95 Ligand EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human FASL/CD95LG/CD95 Ligand EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292172026-03-10T04:39:52+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1618.pngMouse PGLYRP1/Pgrps EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse PGLYRP1/Pgrps EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292182026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0535.pngHuman uPA/PLAU/URK EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human uPA/PLAU/URK EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292192026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0331.pngHuman CCL24/Eotaxin-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CCL24/Eotaxin-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292202026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1125.pngMouse CCL6/C10 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CCL6/C10 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292212026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0755.pngHuman EPCAM/Trop1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human EPCAM/Trop1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292222026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0430.pngHuman IL-17/IL-17A EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human IL-17/IL-17A EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292232026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0377.pngRat IGF-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat IGF-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292242026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0378.pngMouse IGF-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse IGF-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292252026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2107.pngMouse Plasma Kallikrein/KLKB1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Plasma Kallikrein/KLKB1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292262026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1383.pngHuman TGFBR3/Tgf Beta Riii EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TGFBR3/Tgf Beta Riii EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292272026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0447.pngMouse CCL22/MDC EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CCL22/MDC EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292282026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1989.pngMouse STC2/Stanniocalcin 2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse STC2/Stanniocalcin 2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292292026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1844.pngHuman JAM-C EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human JAM-C EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292302026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0914.pngHuman Clusterin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Clusterin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292312026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1939.pngHuman CA4/Carbonic anhydrase 4 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CA4/Carbonic anhydrase 4 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292322026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1711.pngMouse Serpin A1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Serpin A1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292332026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0577.pngMouse Gp130/IL6ST EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Gp130/IL6ST EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292342026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1943.pngHuman CLEC11A EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CLEC11A EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292352026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1739.pngHuman PROS1/Protein S EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human PROS1/Protein S EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292362026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1413.pngHuman CD5L/CT-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CD5L/CT-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292372026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1353.pngHuman Neuropilin-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Neuropilin-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292382026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1466.pngHuman Hemopexin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Hemopexin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292392026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0501.pngHuman sE-Selectin/CD62E EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human sE-Selectin/CD62E EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292402026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2145.pngHuman complement C3a EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human complement C3a EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292412026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1327.pngRat Adiponectin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat Adiponectin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292422026-03-10T04:39:53+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0967.pngHuman LYVE-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human LYVE-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292432026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1954.pngHuman Complement C1R EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Complement C1R EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292442026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0757.pngHuman Fetuin A/AHSG EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Fetuin A/AHSG EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292452026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0644.pngHuman Endoglin/CD105/ENG EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Endoglin/CD105/ENG EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292462026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0829.pngHuman RANK EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human RANK EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292472026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1240.pngHuman Galectin-3BP EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Galectin-3BP EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292482026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1881.pngHuman CTRP9 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CTRP9 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292492026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0867.pngHuman DKK-1/Dickkopf 1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human DKK-1/Dickkopf 1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292502026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0475.pngHuman NT-4/NTF4/Neurotrophin-4 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human NT-4/NTF4/Neurotrophin-4 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292512026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0482.pngHuman OPN/Osteopontin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human OPN/Osteopontin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292522026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0960.pngHuman ANGPTL4/Angiopoietin Like 4/ARP4 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human ANGPTL4/Angiopoietin Like 4/ARP4 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292532026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0730.pngMouse CXCL7/PPBP EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CXCL7/PPBP EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292542026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1812.pngHuman REG1A EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human REG1A EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292552026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2062.pngRat MAG EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat MAG EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292562026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0582.pngMouse Resistin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse Resistin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292572026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2123.pngHuman LILRB1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human LILRB1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292582026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0442.pngHuman CCL8/MCP-2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CCL8/MCP-2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292592026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2136.pngHuman ZAG/AZGP1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human ZAG/AZGP1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292602026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0920.pngHuman TNFSF12/Tweak EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TNFSF12/Tweak EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292612026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0533.pngHuman TRAILR3/TNFRSF10C EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TRAILR3/TNFRSF10C EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292622026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0684.pngHuman CCL17/TARC EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CCL17/TARC EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292632026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1255.pngHuman CD320/8D6A/TCblR EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CD320/8D6A/TCblR EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292642026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1315.pngHuman CD21/CR2 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CD21/CR2 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292652026-03-10T04:39:54+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1765.pngHuman PAM EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human PAM EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292662026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1114.pngHuman Granzyme B EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Granzyme B EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292672026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1653.pngHuman Properdin/Complement Factor P EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Properdin/Complement Factor P EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292682026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0844.pngHuman TREM-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human TREM-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292692026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2033.pngMouse CHIT1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CHIT1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292702026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0372.pngRat ICAM-1 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat ICAM-1 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292712026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez2052.pngHuman CD69 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CD69 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292722026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0978.pngRat CRP/C Reactive Protein EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat CRP/C Reactive Protein EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292732026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1184.pngMouse ALCAM/CD166 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse ALCAM/CD166 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292742026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1572.pngRat ALCAM/CD166 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat ALCAM/CD166 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292752026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0456.pngHuman CCL19/MIP-3 Beta EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human CCL19/MIP-3 Beta EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292762026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1634.pngHuman Serpin A1/alpha 1-Antitrypsin EZ-Set™ ELISA Kit (DIY Antibody Pairs)Human Serpin A1/alpha 1-Antitrypsin EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292772026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez1209.pngRat SAP/PTX2/APCS EZ-Set™ ELISA Kit (DIY Antibody Pairs)Rat SAP/PTX2/APCS EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292782026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0703.pngMouse CD40/TNFRSF5 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse CD40/TNFRSF5 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/catalog/product/view/id/1292792026-03-10T04:39:55+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/e/z/ez0930.pngMouse IL-33 EZ-Set™ ELISA Kit (DIY Antibody Pairs)Mouse IL-33 EZ-Set ELISA Kit standard curve https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-abce1-picoband-antibody-azq6tnw3-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azq6tnw3-abce1-primary-antibodies-wb-testing-1.jpgAnti-Zebrafish ABCE1 Antibody Picoband® Western blot analysis of Zebrafish ABCE1 using anti-Zebrafish ABCE1 antibody (AZQ6TNW3). Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: Zebrafish embryo tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Zebrafish ABCE1 antigen affinity purified polyclonal antibody (AZQ6TNW3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Zebrafish ABCE1 at approximately 67 kDa. The expected band size for Zebrafish ABCE1 is at 67 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azq6tnw3-abce1-primary-antibodies-ihc-testing-2.jpgAnti-Zebrafish ABCE1 Antibody Picoband® IHC analysis of Zebrafish ABCE1 using anti-Zebrafish ABCE1 antibody (AZQ6TNW3). Zebrafish ABCE1 was detected in paraffin-embedded section of zebrafish brain tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Zebrafish ABCE1 Antibody (AZQ6TNW3) overnight at 4°C.Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azq6tnw3-abce1-primary-antibodies-ihc-testing-3.jpgAnti-Zebrafish ABCE1 Antibody Picoband® IHC analysis of Zebrafish ABCE1 using anti-Zebrafish ABCE1 antibody (AZQ6TNW3). Zebrafish ABCE1 was detected in paraffin-embedded section of zebrafish eye tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Zebrafish ABCE1 Antibody (AZQ6TNW3) overnight at 4°C.Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-afg3l2-picoband-antibody-aza9jrg9-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/aza9jrg9-afg3l2-primary-antibodies-ihc-testing-1.jpgAnti-Zebrafish AFG3L2 Antibody Picoband® Western blot analysis of Zebrafish AFG3L2 using anti-Zebrafish AFG3L2 antibody (AZA9JRG9). Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: Zebrafish head tissue lysates, Lane 2: Zebrafish embryo tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Zebrafish AFG3L2 antigen affinity purified polyclonal antibody (AZA9JRG9) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Zebrafish AFG3L2 at approximately 80-90 kDa. The expected band size for Zebrafish AFG3L2 is at 89 kDa. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-ago4-picoband-antibody-azk4iah1-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azk4iah1-ago4-primary-antibodies-ihc-testing-1.jpgAnti-Zebrafish AGO4 Antibody Picoband® IHC analysis of Zebrafish AGO4 using anti-Zebrafish AGO4 antibody (AZK4IAH1). Zebrafish AGO4 was detected in paraffin-embedded section of zebrafish cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Zebrafish AGO4 Antibody (AZK4IAH1) overnight at 4°C.Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-atg5-picoband-antibody-azf1rdc0-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azf1rdc0-atg5-primary-antibodies-ihc-testing-1.jpgAnti-Zebrafish ATG5 Antibody Picoband® IHC analysis of Zebrafish ATG5 using anti-Zebrafish ATG5 antibody (AZF1RDC0). Zebrafish ATG5 was detected in paraffin-embedded section of zebrafish cerebellum tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Zebrafish ATG5 Antibody (AZF1RDC0) overnight at 4°C.Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-bag5-picoband-antibody-azf1qgm6-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azf1qgm6-bag5-primary-antibodies-wb-testing-1.jpgAnti-Zebrafish BAG5 Antibody Picoband® Western blot analysis of Zebrafish BAG5 using anti-Zebrafish BAG5 antibody (AZF1QGM6). Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: Zebrafish tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Zebrafish BAG5 antigen affinity purified polyclonal antibody (AZF1QGM6) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Zebrafish BAG5 at approximately 50 kDa. The expected band size for Zebrafish BAG5 is at 57 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azf1qgm6-bag5-primary-antibodies-ihc-testing-2.jpgAnti-Zebrafish BAG5 Antibody Picoband® IHC analysis of Zebrafish BAG5 using anti-Zebrafish BAG5 antibody (AZF1QGM6). Zebrafish BAG5 was detected in paraffin-embedded section of zebrafish heart tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Zebrafish BAG5 Antibody (AZF1QGM6) overnight at 4°C.Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-c1qbp-picoband-antibody-azf1r3f7-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azf1r3f7-c1qbp-primary-antibodies-wb-testing-1.jpgAnti-Zebrafish C1QBP Antibody Picoband® Western blot analysis of Zebrafish C1QBP using anti-Zebrafish C1QBP antibody (AZF1R3F7). Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: Zebrafish tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Zebrafish C1QBP antigen affinity purified polyclonal antibody (AZF1R3F7) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Zebrafish C1QBP at approximately 35 kDa. The expected band size for Zebrafish C1QBP is at 30 kDa. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-cct2-picoband-antibody-azq6pbw6-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azq6pbw6-cct2-primary-antibodies-wb-testing-1.jpgAnti-Zebrafish CCT2 Antibody Picoband® Western blot analysis of Zebrafish CCT2 using anti-Zebrafish CCT2 antibody (AZQ6PBW6). Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: Zebrafish tissue lysates, Lane 2: Zebrafish embryo tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Zebrafish CCT2 antigen affinity purified polyclonal antibody (AZQ6PBW6) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Zebrafish CCT2 at approximately 58 kDa. The expected band size for Zebrafish CCT2 is at 58 kDa. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-cct5-picoband-antibody-azq6nvi6-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azq6nvi6-cct5-primary-antibodies-wb-testing-1.jpgAnti-Zebrafish CCT5 Antibody Picoband® Western blot analysis of Zebrafish CCT5 using anti-Zebrafish CCT5 antibody (AZQ6NVI6). Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: Zebrafish head tissue lysates, Lane 2: Zebrafish embyro tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Zebrafish CCT5 antigen affinity purified polyclonal antibody (AZQ6NVI6) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Zebrafish CCT5 at approximately 59 kDa. The expected band size for Zebrafish CCT5 is at 59 kDa. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-cul1a-b-picoband-antibody-azq6nys3-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azq6nys3-cul1ab-primary-antibodies-wb-testing-1.jpgAnti-Zebrafish CUL1A/B Antibody Picoband® Western blot analysis of Zebrafish CUL1A/B using anti-Zebrafish CUL1A/B antibody (AZQ6NYS3). Electrophoresis was performed on a 10% SDS-PAGE gel at 70V (Stacking gel) / 90V (Resolving gel) for 2-3 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: Zebrafish head tissue lysates, Lane 2: Zebrafish embyro tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-Zebrafish CUL1A/B antigen affinity purified polyclonal antibody (AZQ6NYS3) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an Enhanced Chemiluminescent detection (ECL) kit (Catalog # EK1002) with Tanon 5200 system. A specific band was detected for Zebrafish CUL1A/B at approximately 80-90 kDa. The expected band size for Zebrafish CUL1A/B is at 90 kDa. https://www.bosterbio.com/products/primary-antibodies/zebrafish-antibodies/anti-dmrt1-picoband-antibody-azq71mm5-boster.html2026-03-17T05:16:26+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/z/azq71mm5-dmrt1-primary-antibodies-ihc-testing-1.jpgAnti-Zebrafish DMRT1 Antibody Picoband® IHC analysis of Zebrafish DMRT1 using anti-Zebrafish DMRT1 antibody (AZQ71MM5). Zebrafish DMRT1 was detected in paraffin-embedded section of zebrafish ovary tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2μg/ml rabbit anti-Zebrafish DMRT1 Antibody (AZQ71MM5) overnight at 4°C.Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen. https://www.bosterbio.com/catalog/product/view/id/1292942026-03-17T05:16:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17241-1-tmem232-primary-antibodies-wb-testing-1.jpgAnti-TMEM232 Antibody Picoband® Western blot analysis of TMEM232 using anti-TMEM232 antibody (A17241-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human Jurkat whole cell lysates, Lane 3: human U251 whole cell lysates, Lane 4: human PC-3 whole cell lysates, Lane 5: rat testis tissue lysates, Lane 6: rat brain tissue lysates, Lane 7: mouse testis tissue lysates, Lane 8: mouse brain tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TMEM232 antigen affinity purified polyclonal antibody (A17241-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TMEM232 at approximately 76 kDa. The expected band size for TMEM232 is at 76 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17241-1-tmem232-primary-antibodies-ihc-testing-2.jpgAnti-TMEM232 Antibody Picoband® IHC analysis of TMEM232 using anti-TMEM232 antibody (A17241-1). TMEM232 was detected in a paraffin-embedded section of human colon tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TMEM232 Antibody (A17241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17241-1-tmem232-primary-antibodies-ihc-testing-3.jpgAnti-TMEM232 Antibody Picoband® IHC analysis of TMEM232 using anti-TMEM232 antibody (A17241-1). TMEM232 was detected in a paraffin-embedded section of human colon cancer tissue. Heat mediated antigen retrieval was performed in EDTA buffer (pH 8.0, epitope retrieval solution). The tissue section was blocked with 10% goat serum. The tissue section was then incubated with 2 μg/ml rabbit anti-TMEM232 Antibody (A17241-1) overnight at 4°C. Peroxidase Conjugated Goat Anti-rabbit IgG was used as secondary antibody and incubated for 30 minutes at 37°C. The tissue section was developed using HRP Conjugated Rabbit IgG Super Vision Assay Kit (Catalog # SV0002) with DAB as the chromogen.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a17241-1-tmem232-primary-antibodies-if-testing-4.jpgAnti-TMEM232 Antibody Picoband® IF analysis of TMEM232 using anti-TMEM232 antibody (A17241-1). TMEM232 was detected in an immunocytochemical section of SIHA cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TMEM232 Antibody (A17241-1) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) was used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. The section was counterstained with DAPI. Visualize using a fluorescence microscope and filter sets appropriate for the label used. https://www.bosterbio.com/catalog/product/view/id/1292952026-03-17T05:16:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06035-1-tox3-primary-antibodies-wb-testing-1.jpgAnti-TOX3 Antibody Picoband® Western blot analysis of TOX3 using anti-TOX3 antibody (A06035-1). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human SH-SY5Y whole cell lysates, Lane 2: human A431 whole cell lysates, Lane 3: human RT4 whole cell lysates, Lane 4: human HepG2 whole cell lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-TOX3 antigen affinity purified polyclonal antibody (A06035-1) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for TOX3 at approximately 69 kDa. The expected band size for TOX3 is at 63 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06035-1-tox3-primary-antibodies-if-testing-2.jpgAnti-TOX3 Antibody Picoband® IF analysis of TOX3 using anti-TOX3 antibody (A06035-1) and anti-Beta Tubulin antibody (M01857-3). TOX3 was detected in an immunocytochemical section of U2OS cells. Enzyme antigen retrieval was performed using IHC enzyme antigen retrieval reagent (AR0022) for 15 mins. The cells were blocked with 10% goat serum. And then incubated with 5 μg/mL rabbit anti-TOX3 Antibody (A06035-1) and mouse anti-Beta Tubulin antibody (M01857-3) overnight at 4°C. DyLight®488 Conjugated Goat Anti-Rabbit IgG (BA1127) and Cy3 Conjugated Goat Anti-Mouse IgG (BA1031) were used as secondary antibody at 1:500 dilution and incubated for 30 minutes at 37°C. Visualize using a fluorescence microscope and filter sets appropriate for the label used.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/0/a06035-1-tox3-primary-antibodies-fcm-testing-3.jpgAnti-TOX3 Antibody Picoband® Flow Cytometry analysis of HepG2 cells using anti-TOX3 antibody (A06035-1). Overlay histogram showing HepG2 cells stained with A06035-1 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-TOX3 Antibody (A06035-1, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control. https://www.bosterbio.com/catalog/product/view/id/1292962026-03-17T05:16:27+00:00daily0.9https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13578-2-serpinb12-primary-antibodies-wb-testing-1.jpgAnti-SERPINB12 Antibody Picoband® Western blot analysis of SERPINB12 using anti-SERPINB12 antibody (A13578-2). Electrophoresis was performed on a 10% SDS-PAGE gel at 80V (Stacking gel) / 120V (Resolving gel) for 2 hours. The sample well of each lane was loaded with 30 ug of sample under reducing conditions. Lane 1: human K562 whole cell lysates, Lane 2: human Hela whole cell lysates, Lane 3: human SIHA whole cell lysates, Lane 4: human U251 whole cell lysates, Lane 5: mouse brain tissue lysates, Lane 6: mouse heart tissue lysates. After electrophoresis, proteins were transferred to a nitrocellulose membrane at 150 mA for 50-90 minutes. Blocked the membrane with 5% non-fat milk/TBS for 1.5 hour at RT. The membrane was incubated with rabbit anti-SERPINB12 antigen affinity purified polyclonal antibody (A13578-2) at 0.5 μg/mL overnight at 4°C, then washed with TBS-0.1%Tween 3 times with 5 minutes each and probed with a goat anti-rabbit IgG-HRP secondary antibody at a dilution of 1:5000 for 1.5 hour at RT. The signal is developed using an ECL Plus Western Blotting Substrate (Catalog # AR1196-200) with Tanon 5200 system. A specific band was detected for SERPINB12 at approximately 46 kDa. The expected band size for SERPINB12 is at 46 kDa.https://www.bosterbio.com/pub/media/catalog/product/cache/ac8b64ee610939d0b5d6545d1a7fa448/a/1/a13578-2-serpinb12-primary-antibodies-fcm-testing-2.jpgAnti-SERPINB12 Antibody Picoband® Flow Cytometry analysis of RT4 cells using anti-SERPINB12 antibody (A13578-2). Overlay histogram showing RT4 cells stained with A13578-2 (Blue line). To facilitate intracellular staining, cells were fixed with 4% paraformaldehyde and permeabilized with permeabilization buffer. The cells were blocked with 10% normal goat serum. And then incubated with rabbit anti-SERPINB12 Antibody (A13578-2, 1 μg/1x106 cells) for 30 min at 20°C. DyLight®488 conjugated goat anti-rabbit IgG (BA1127, 5-10 μg/1x106 cells) was used as secondary antibody for 30 minutes at 20°C. Isotype control antibody (Green line) was rabbit IgG (1 μg/1x106) used under the same conditions. Unlabelled sample without incubation with primary antibody and secondary antibody (Red line) was used as a blank control.